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Previous literature suggests that acute opioid use results in the functional impairment of the immune response, thereby decreasing resistance to viral infection. Here, we assessed if innate and adaptive immune responses are compromised ex vivo in persons who inject drugs (PWID) and whether long-term injection drug use may impact host susceptibility to in vitro HIV infection. We measured the frequency, activation state, and functional profile of NK cells, dendritic cells, and CD4+ and CD8+ T cells in low-risk PWID who do not share needles, high-risk needle-sharing PWID, and control donors who did not inject drugs. We also assessed plasma levels of inflammatory markers and CD4+ T cell susceptibility to HIV infection. We observed a significant increase in the amount of sCD14 (P = 0.0023, n = 16) and sCD163 (P = 0.0001, n = 16) in the plasma of PWID compared to controls. Evidence of constitutive activation was noted in PWID as compared to controls with increased CD69 expression in CD56dim NK cells (P = 0.0103, n = 26) and increased CD38 and HLA-DR expression in CD4+ T cells (P = 0.0355, n = 23). However, no innate or adaptive functional differences were detected between PWID and controls, including: NK cell direct or antibody-dependent cellular cytotoxicity poly-functional response, TLR-stimulated dendritic cell/NK crosstalk, CD8+ T cell response to Staphylococcal enterotoxin B or CMV/EBV/FLU peptides, or constitutive or anti-CD3/CD28-stimulated CD4+ T cell infectivity with CCR5-tropic or CXCR4-tropic HIV-1 isolates. Our data indicate that PWID who utilize opioids over as prolonged time frame can retain a functional ex vivo immune response without a measurable increase in CD4+ T cell infectivity suggesting that leukocytes from PWID are not intrinsically more susceptibility to infection with HIV than non-PWID controls.

The ultrastructure of the pseudobranch of the euryhaline, self-fertilizing fish, Rivulus marmoratus (Cyprinodontidae) was studied with thin sectio and freeze-fracture transmission electron microscopy. In specimens raised from birth in 1% or 200% seawater, the pseudobranch contains two mitochondria-rich cell types, pseudobranchial cells and chloride cells, each of which has an extensive tubular system. Chloride cells only occur on the lateral aspects of the pseudobranch, with their apical crypts open to the environment. Apical crypt invagination to a “pit” structure and multicellular complexes occur in both salinity extremes. The ultrastructure of chloride cells in 1% and 200% SW is consistent with that described previously in the opercular epithelium, opercular skin, and gill of this species; elaboration of mitochondria and basolateral membrane accompanies increased environmental salinity (King et al.: Cell and Tissue Research 257:367–377, 1989). Pseudobranchial cells constitute the majority of the cells; they do not extend to the surface but have a more organized tubular system that is continuous with the basal membrane. These cells do not exhibit ultrastructural changes in response to increased salinity. © 1993 Wiley-Liss, Inc.

Ultraviolet light and the heavy metal, cadmium, both have toxic effects on many microorganisms. In this communication we describe a method by which the bacterium Klebsiella aerogenes surmounts both problems using one biological process: the synthesis of cadmium sulfide (CdS) crystallites. These semiconductor particles absorb radiation in the UV spectral region and therefore, when K. aerogenes produces extracellular CdS material in response to environments containing cadmium ions, a photoprotective layer is formed. The effect of UVA radiation on cultures of Klebsiella aerogenes was monitored using electron microscopy, energy-dispersive X-ray analysis and electronic spectroscopy. The results show that at wavelengths 320 nm Λ 400 nm, a photoprotection period of between 4 and 6 h is induced, which eventually fails due to photodegradation of the semiconductor layer to metallic cadmium and elemental sulfur.

Proton-gated Na(+) channels (ASIC) are new members of the epithelial sodium channel/degenerin gene family. ASIC3 mRNA has been detected in the homogenate of pulmonary tissues. However, whether ASIC3 is expressed in the apical membranes of lung epithelial cells and whether it regulates cystic fibrosis transmembrane conductance regulator (CFTR) function are not known at the present time. Using reverse transcription-PCR, we found that the ASIC3 mRNA was expressed in the human airway mucosal gland (Calu-3) and human airway epithelial (16HBE14o) cells. Indirect immunofluorescence microscopy revealed that ASIC3 was co-segregated with CFTR in the apical membranes of Calu-3 cells. Proton-gated, amiloride-sensitive short circuit Na(+) currents were recorded across Calu-3 monolayers mounted in an Ussing chamber. In whole-cell patch clamp studies, activation of CFTR channels with cAMP reduced proton-gated Na(+) current in Calu-3 cells from -154 +/- 28 to -33 +/- 16 pA (n = 5, p0.05) at -100 mV. On the other hand, cAMP-activated CFTR activity was significantly inhibited following constitutive activation of putative ASIC3 at pH 6.0. Immunoassays showed that both ASIC3 and CFTR proteins were expressed and co-immunoprecipitated mutually in Calu-3 cells. Similar results were obtained in human embryonic kidney 293T cells following transient co-transfection of ASIC3 and CFTR. Our results indicate that putative CFTR and ASIC3 channels functionally interact with each other, possibly via an intermolecular association. Because acidic luminal fluid in the cystic fibrosis airway and lung tends to stimulate ASIC3 channel expression and activity, the interaction of ASIC3 and CFTR may contribute to defective salt and fluid transepithelial transport in the cystic fibrotic pulmonary system.

The interaction of ion channels with the actin-based cytoskeleton in epithelial cells not only maintains the polarized expression of ion channels within specific membrane domains, it also functions in the intracellular trafficking and regulation of channel activity. Initial evidence supporting an interaction between epithelial ion channels and the actin-based cytoskeleton came from patch-clamp studies examining the effects of cytochalasins on channel activity. Cytochalasins were shown to either activate or inactivate epithelial ion channels. An interaction between the actin-based cytoskeleton and epithelial ion channels was further supported by the fact that the addition of monomeric or filamentous actin to excised patches had an effect on channel activity comparable to that of cytochalasins. Through the recent application of molecular and proteomic approaches, we now know that the interactions between epithelial ion channels and actin can either be direct or indirect, the latter being mediated through scaffolding or actin-binding proteins that serve as links between the channels and the actin-based cytoskeleton. This review discusses recent advances in our understanding of the interactions between epithelial ion channels and the actin-based cytoskeleton, and the roles these interactions play in regulating the cell surface expression, activity, and intracellular trafficking of epithelial ion channels.

The activity of the amiloride-sensitive epithelial sodium channel (ENaC) is modulated by F-actin. However, it is unknown if there is a direct interaction between alpha-ENaC and actin. We have investigated the hypothesis that the actin cytoskeleton directly binds to the carboxyl terminus of alpha-ENaC using a combination of confocal microscopy, co-immunoprecipitation, and protein binding studies. Confocal microscopy of Madin-Darby canine kidney cell monolayers stably transfected with wild type, rat isoforms of alpha-, beta-, and gamma-ENaC revealed co-localization of alpha-ENaC with the cortical F-actin cytoskeleton both at the apical membrane and within the subapical cytoplasm. F-actin was found to co-immunoprecipitate with alpha-ENaC from whole cell lysates of this cell line. Gel overlay assays demonstrated that F-actin specifically binds to the carboxyl terminus of alpha-ENaC. A direct interaction between F-actin and the COOH terminus of alpha-ENaC was further corroborated by F-actin co-sedimentation studies. This is the first study to report a direct and specific biochemical interaction between F-actin and ENaC.

Lovastatin, an inhibitor of the rate-limiting enzyme in cholesterol biosynthesis, is widely used to treat hypercholesterolemia. We investigated the long-term effects of lovastatin alone and in combination with ursodeoxycholic acid on biliary lipid composition and gallstone dissolution. Forty-two prairie dogs were fed 1.2% cholesterol diet for 5 weeks, and cholecystectomy was performed on 6 animals to confirm gallstones. The remaining animals were maintained on a 0.4% cholesterol diet and were randomized to receive placebo, lovastatin (3.3 mg/g diet), ursodeoxycholic acid (10 mg/g), or combination of both drugs. After 10 weeks, animals underwent cholecystectomy. Dissolution response to therapy was determined, and serum and biliary lipids were measured. All treatment groups had significant reductions in serum cholesterol. Lovastatin treatment reduced both hepatic and gallbladder bile cholesterol, altered bile acid composition, and induced a 79% total response compared to placebo. Although ursodeoxycholic treatment induced a 44% response, long-term combination treatment elevated both gallbladder bile cholesterol and calcium and failed to produce an augmented response. These data suggest that lovastatin therapy alone may promote gallstone dissolution in humans.

The renal epithelial cell line A6, derived from Xenopus laevis, expresses epithelial Na+channels (ENaCs) and serves as a model system to study hormonal regulation and turnover of ENaCs. Our previous studies suggest that the α-subunit of Xenopus ENaC (α- xENaC) is detectable as 150- and 180-kDa polypeptides, putative immature and mature α-subunit heterodimers. The 150- and 180-kDa α- xENaC were present in distinct fractions after sedimentation of A6 cell lysate through a sucrose density gradient. Two anti-α- xENaC antibodies directed against distinct domains demonstrated that only 180-kDa α- xENaC was expressed at the apical cell surface. The half-life of cell surface-expressed α- xENaC was 24–30 h, suggesting that once ENaC matures and is expressed at the plasma membrane, its turnover is similar to that reported for mature cystic fibrosis transmembrane conductance regulator. No significant changes in apical surface expression of α- xENaC were observed after treatment of A6 cells with aldosterone for 24 h, despite a 5.3-fold increase in short-circuit current. This lack of change in surface expression is consistent with previous observations in A6 cells and suggests that aldosterone regulates ENaC gating and increases channel open probability.

Gallbladder Na+ absorption is linked to gallstone formation in prairie dogs. Na+/H+ exchange (NHE) is one of the major Na+ absorptive pathways in gallbladder. In this study, we measured gallbladder Na+/H+ exchange and characterized the NHE isoforms expressed in prairie dogs. Na+/H+ exchange activity was assessed by measuring amiloride-inhibitable transepithelial Na+ flux and apical 22Na+ uptake using dimethylamiloride (DMA). HOE-694 was used to determine NHE2 and NHE3 contributions. Basal JNams was higher than JNasm with JNanet absorption. Mucosal DMA inhibited transepithelial Na+ flux in a dose-dependent fashion, causing JNams equal to JNasm and blocking JNanet absorption at 100 μm. Basal 22Na+ uptake rate was 10.9 ± 1.0 μmol · cm−2· hr−1 which was inhibited by ∼43% by mucosal DMA and ∼30% by mucosal HOE-694 at 100 μm. RT-PCR and Northern blot analysis demonstrated expression of mRNAs encoding NHE1, NHE2 and NHE3 in the gallbladder. Expression of NHE1, NHE2 and NHE3 polypeptides was confirmed using isoform-specific anti-NHE antibodies. These data suggest that Na+/H+ exchange accounts for a substantial fraction of gallbladder apical Na+ entry and most of net Na+ absorption in prairie dogs. The NHE2 and NHE3 isoforms, but not NHE1, are involved in gallbladder apical Na+ uptake and transepithelial Na+ absorption.

The mammalian urinary bladder exhibits transepithelial Na+absorption that contributes to Na+gradients established by the kidney. Electrophysiological studies have demonstrated that electrogenic Na+absorption across the urinary bladder is mediated in part by amiloride-sensitive Na+channels situated within the apical membrane of the bladder epithelium. We have used a combination of in situ hybridization, Northern blot analysis, and immunocytochemistry to examine whether the recently cloned epithelial Na+channel (ENaC) is expressed in the rat urinary bladder. In situ hybridization and Northern blot analyses indicate that α-, β-, and γ-rat ENaC (rENaC) are expressed in rat urinary bladder epithelial cells. Quantitation of the levels of α-, β-, and γ-rENaC mRNA expression in rat urinary bladder, relative to β-actin mRNA expression, indicates that, although comparable levels of α- and β-rENaC subunits are expressed in the urinary bladder of rats maintained on standard chow, the level of γ-rENaC mRNA expression is 5- to 10-fold lower than α- or β-rENaC mRNA. Immunocytochemistry, using an antibody directed against α-rENaC, revealed that ENaCs are predominantly localized to the luminal membrane of the bladder epithelium. Together, these data demonstrate that ENaC is expressed in the mammalian urinary bladder and suggest that amiloride-sensitive Na+transport across the apical membrane of the mammalian urinary bladder epithelium is mediated primarily by ENaC.

The toad urinary bladder and epithelial cell lines derived from the urinary bladder, including TBM, serve as model systems for the study of transepithelial Na+ transport. We examined biochemical characteristics of epithelial Na+ channels in toad urinary bladder and TBM cells and their cellular localization in the urinary bladder. The radiolabeled amiloride analogue [3H]benzamil bound to a single class of high-affinity binding sites in membrane vesicles from toad urinary bladder with a dissociation constant (Kd) of 10 nM. Photoactive benzamil analogues specifically labeled a 135,000-Da polypeptide in toad urinary bladder and TBM cells. A monoclonal anti-Na+ channel antibody directed against the amiloride-binding component of the channel specifically recognized a 135,000-Da polypeptide in TBM cells. Polyclonal anti-Na+ channel antibodies generated against purified bovine epithelial Na+ channel specifically recognized a 235,000-Da polypeptide in toad urinary bladder and localized Na+ channels to the apical plasma membrane of urinary bladder epithelial cells. The biochemical characteristics and the cellular localization of epithelial Na+ channels in toad urinary bladder are similar to those previously described in mammalian kidney and in the A6 cell line.

The transforming growth factor β (TGFB) superfamily proteins bone morphogenetic protein 15 (BMP15) and growth differentiation factor 9 (GDF9), are essential for mammalian fertility. Recent in vitro evidence suggests that the proregions of mouse BMP15 and GDF9 interact with their mature proteins after secretion. In this study, we have actively immunized mice against these proregions to test the potential in vivo roles on fertility. Mice were immunized with either N- or C-terminus proregion peptides of BMP15 or GDF9, or a full-length GDF9 proregion protein, each conjugated to keyhole limpet hemocyanin (KLH). For each immunization group, ovaries were collected from ten mice for histology after immunization, while a further 20 mice were allowed to breed and litter sizes were counted. To link the ovulation and fertility data of these two experimental end points, mice were joined during the time period identified by histology as being the ovulatory period resulting in to the corpora lutea (CL) counted. Antibody titers in sera increased throughout the study period, with no cross-reactivity observed between BMP15 and GDF9 sera and antigens. Compared with KLH controls, mice immunized with the N-terminus BMP15 proregion peptide had ovaries with fewer CL (PPPP

To determine the mechanism by which vasopressin increases apical membrane Na+ entry, we evaluated whether or not this hormone could recruit Na+ channels from a subapical membrane pool using specific polyclonal antibodies raised against high amiloride affinity bovine renal papillary Na+ channels. We also studied the effect of protein kinase A (PKA)-mediated phosphorylation on single-channel activity of highly purified Na+ channels incorporated into planar lipid bilayer membranes. PKA induced a significant increase in open-channel probability (Po) with no change in single-channel conductance. As shown previously and reconfirmed in the present work, PKA catalyzed the phosphorylation of a single subunit of this Na+ channel protein, namely, a 300-kDa polypeptide. On the other hand, protein kinase C, in combination with diacylglycerol, Ca2+, and phosphatidylserine, phosphorylated both the 130- and 55-kDa subunits of this purified Na+ channel, with a concomitant decrease in Po of both untreated and previously PKA-treated channels. We also found, in expression studies conducted in confluent monolayers of amphibian renal A6 cells, that vasopressin did not induce the apical insertion of new channel proteins. These observations support the hypothesis that vasopressin increases the apical Na+ permeability by activating Na+ channels already resident in the apical membrane by a direct phosphorylation mechanism rather than by cytoplasmic recruitment of latent Na+ channels.

We examined the development of epithelial Na+ conductance in 6- and 7-day post coitus (p.c.) preimplantation rabbit embryos using the whole-cell patch-clamp technique on dissociated rabbit trophectodermal cells and by immunocytochemical localization using a polyclonal antibody directed against subunits of an apical epithelial Na+ channel on the intact blastocyst. In Day 6 and 7 p.c. trophectodermal cells, we observed an outwardly rectified whole-cell Na+ current. The current-voltage characteristics did not differ between the 6- and the 7-day p.c. cells. Replacement of Na+ with the impermeant cation N-methyl-D-glucamine in the pipette or bath reduced outward currents and inward currents, respectively, indicating that the current was Na(+)-dependent. Treatment of 7-day p.c. cells with 100 microM amiloride, benzamil, or ethylisopropyl amiloride (EIPA) blocked the whole-cell currents within 5 min. However, the current of the Day 6 p.c. embryo was not blocked by amiloride. The amiloride block at Day 7 p.c. was only partially reversible after 15 min of continuous perfusion of the bath with an amiloride-free solution. The apparent dissociation constant (Ki) for amiloride, benzamil, and EIPA was 12, 50, and 16 microM, respectively, when measured 5 min after drug addition. Immunolocalization studies of blastocysts with a polyclonal antibody raised against a high amiloride affinity Na+ channel isolated from bovine kidney revealed no specific binding to the trophectodermal cells at Day 6 p.c.(ABSTRACT TRUNCATED AT 250 WORDS)

Pleural effusions are commonly clinical disorders, resulting from the imbalance between pleural fluid turnover and reabsorption. The mechanisms underlying pleural fluid clearance across the mesothelium remain to be elucidated. We hypothesized that epithelial Na(+) channel (ENaC) is expressed and forms the molecular basis of the amiloride-sensitive resistance in human mesothelial cells. Our RT-PCR results showed that three ENaC subunits, namely, alpha, beta, gamma, and two delta ENaC subunits, are expressed in human primary pleural mesothelial cells, a human mesothelioma cell line (M9K), and mouse pleural tissue. In addition, Western blotting and immunofluorescence microscopy studies revealed that alpha, beta, gamma, and delta ENaC subunits are expressed in primary human mesothelial cells and M9K cells at the protein level. An amiloride-inhibitable short-circuit current was detected in M9K monolayers and mouse pleural tissues when mounted in Ussing chambers. Whole-cell patch clamp recordings showed an ENaC-like channel with an amiloride concentration producing 50% inhibition of 12 microM in M9K cells. This cation channel has a high affinity for extracellular Na+ ions (K(m): 53 mM). The ion selectivity of this channel to cations follows the same order as ENaC: Li+Na+K+. The unitary Li(+) conductance was 15 pS in on-cell patches. Four ENaC subunits form a functional Na+ channel when coinjected into Xenopus oocytes. Furthermore, we found that both forskolin and cGMP increased the short-circuit currents in mouse pleural tissues. Taken together, our data demonstrate that the ENaC channels are biochemically and functionally expressed in human pleural mesothelial cells, and can be up-regulated by cyclic AMP and cyclic GMP.

Transtrophectodermal 3-0-methyl glucose (3-0MG) transport in the rabbit blastocyst at Days 6 and 7 post coitum was investigated to understand better how the trophectoderm can regulate inner cell mass growth by controlling substrate availability. 3-0MG rapidly traversed the trophectoderm and displayed saturation kinetics (Km = 4.3 +/- 0.5 mM, Vmax = 79 +/- 3.8 nmol.cm-2). The flux of 3-0MG was inhibited nearly 95% by 10(-4) M-phloretin, and only 15% by 10(-4) M-phlorizin. Furthermore, 3-0MG influx was inhibited by cytochalasin B (5 microM) and was unaffected by removal of sodium. The transport system had a high specificity for 2-deoxy-D-glucose and glucose, and a very low specificity for fructose and 4-alpha-methyl glucoside. Western blots probed with a polyclonal antibody to the human erythrocyte glucose transport protein and also with a polyclonal antibody to the C-terminus of the glucose transport protein of the rat brain revealed a broad band with a molecular weight of 55,000. Using immuno-gold labelling techniques, Na(+)-independent glucose transporters were localized to both the apical and basolateral borders of the trophectodermal cell. These results suggest that the mechanism in the trophectoderm responsible for transport of glucose is similar to other sodium-independent glucose transport systems. In addition, 3-0MG influx was unaffected by short-term incubation with progesterone, the progesterone antagonist mifepristone (RU-486), PGF-2 alpha, PGE-2, insulin, or cAMP. Day-7 p.c. embryos also transported hexoses by a similar system because the influx rate and the phlorizin/phloretin sensitivity were the same as in the Day-6 p.c. embryo.

Shroom is a recently-described regulator of cell shape changes in the developing nervous system. This protein is a member of a small family of related proteins that are defined by sequence similarity and in most cases by some link to the actin cytoskeleton. At present these proteins are named Shroom, APX, APXL, and KIAA1202. In light of the growing interest in this family of proteins, we propose here a new standard nomenclature.

Gallbladder Na+ absorption and biliary Ca2+ are both increased during gallstone formation and may promote cholesterol nucleation. Na+/H+ exchange (NHE) is a major pathway for gallbladder Na+ transport. Ca2+-dependent second messengers, including protein kinase C (PKC), inhibit basal gallbladder Na+ transport. Multiple PKC isoforms with species- and tissue-specific expression have been reported. In this study we sought to characterize Ca2+-dependent PKC isoforms in gallbladder and to examine their roles in Na+ transport during gallstone formation. Gallbladders were harvested from prairie dogs fed either nonlithogenic chow or 1.2% cholesterol-enriched diet for varying periods to induce various stages of gallstone formation. PKC was activated with the use of phorboldibutyrate, and we assessed gallbladder NHE regulation by measuring unidirectional Na+ flux and dimethylamiloride-inhibitable 22Na+ uptake. We measured gallbladder PKC activity with the use of histone III-S phosphorylation and used Gö 6976 to determine PKC-alpha contributions. Gallbladder PKC isoform messenger RNA and protein expression were examined with the use of Northern- and Western-blot analysis, respectively. Prairie dog and human gallbladder expresses PKC-alpha, betaII, and delta isoforms. The PKC activation significantly decreased gallbladder J(Na)(ms) and reduced baseline 22Na+ uptake by inhibiting NHE. PKC-alpha mediated roughly 42% of total PKC activity under basal conditions. PKC-alpha regulates basal gallbladder Na+ transport by way of stimulation of NHE isoform NHE-2 and inhibition of isoform NHE-3. PKC-alpha blockade reversed PKC-induced inhibition of J(Na)(ms) and 22Na+ uptake by about 45% in controls but was progressively less effective during gallstone formation. PKC-alpha contribution to total PKC activity is progressively reduced, whereas expression of PKC-alpha mRNA, and protein increases significantly during gallstone formation. We conclude that PKC-alpha regulation of gallbladder NHE becomes progressively more dysfunctional and may in part account for the increased Na+ absorption observed during gallstone formation.

The early development of the Atlantic cod, Gadus morhua was studied from fertilization until first-feeding. Multiple families were reared at 7 degrees C and a developmental staging series was prepared using morphological landmarks visible with the light microscope. Stages were named rather than numbered to allow for future additions and broadly grouped into larger time intervals called periods. The most useful staging features were found to be initially cell number, and later in development, somite number. The mean cell cycle time for the first six cleavages was 135 min and the linear regression equation for development of somites(s) over time (t) was s = 0.29t - 18.14. The segmentation period began at 220 h postfertilization (hpf), and unlike some other teleosts, the addition of new somites continued throughout the majority of embryonic development, until just prior to hatching. Hatching occurred at 256 hpf, after which individuals remained motionless at the water's surface, undergoing negative phototaxis only after the first day posthatch. The first-feeding stage was reached at the end of the third day posthatch, subsequent to development of a functional jaw and hindgut. This staging series provides an essential baseline reference for future experiments involving developing cod embryos and for the aquaculture industry.

In this study, the presence of Na(+)-permeable cation channels was determined and characterized in LLC-PK1 cells, a renal tubular epithelial cell line with proximal tubule characteristics derived from pig kidney. Patch-clamp analysis under cell-attached conditions indicated the presence of spontaneously active Na(+)-permeable cation channels. The channels displayed nonrectifying single channel conductance of 11 pS, substates, and an approximately 3:1 Na(+)/K(+) permeability-selectivity ratio. The Na(+)-permeable cation channels were inhibited by pertussis toxin and reactivated by G protein agonists. Cation channel activity was observed in quiescent cell-attached patches after vasopressin stimulation. The addition of protein kinase A and ATP to excised patches also induced Na(+) channel activity. Spontaneous and vasopressin-induced Na(+) channel activity were inhibited by extracellular amiloride. To begin assessing potential molecular candidates for this cation channel, both reverse transcription-PCR and immunocytochemical analyses were conducted in LLC-PK1 cells. Expression of porcine orthologs of the alphaENaC and ApxL genes were found in LLC-PK1 cells. The expression of both gene products was confirmed by immunocytochemical analysis. Although alphaENaC labeling was mostly intracellular, ApxL labeled to both the apical membrane and cytoplasmic compartments of subconfluent LLC-PK1 cells. Vasopressin stimulation had no effect on alphaENaC immunolabeling but modified the cellular distribution of ApxL, consistent with an increased membrane-associated ApxL. The data indicate that proximal tubular LLC-PK1 renal epithelial cells express amiloride-sensitive, Na(+)-permeable cation channels, which are regulated by the cAMP pathway, and G proteins. This channel activity may implicate previously reported epithelial channel proteins, although this will require further experimentation. The evidence provides new clues as to potentially relevant Na(+) transport mechanisms in the mammalian proximal nephron.

the amiloride-sensitive epithelial Na+ channel (ENaC) plays a central role in the reabsorption of salt and fluids across Na+-reabsorbing epithelia such as the distal nephron, distal colon, lungs, and ducts of the exocrine glands. ENaC is rate limiting for net Na+ reabsorption because it mediates

Recent molecular cloning of the epithelial sodium channel (ENaC) provides the opportunity to identify ENaC-associated proteins that function in regulating its cell surface expression and activity. We have examined whether ENaC is associated with Apx (apical protein Xenopus) and the spectrin-based membrane cytoskeleton in Xenopus A6 renal epithelial cells. We have also addressed whether Apx is required for the expression of amiloride-sensitive Na(+) currents by cloned ENaC. Sucrose density gradient centrifugation of A6 cell detergent extracts showed co-sedimentation of xENaC, alpha-spectrin, and Apx. Immunoblot analysis of proteins co-immunoprecipitating under high stringency conditions from peak Xenopus ENaC/Apx-containing gradient fractions indicate that ENaC, Apx, and alpha-spectrin are associated in a macromolecular complex. To examine whether Apx is required for the functional expression of ENaC, alphabetagamma mENaC cRNAs were coinjected into Xenopus oocytes with Apx sense or antisense oligodeoxynucleotides. The two-electrode voltage clamp technique showed there was a marked reduction in amiloride-sensitive current in oocytes coinjected with antisense oligonucleotides when to compared with oocytes coinjected with sense oligonucleotides. These studies indicate that ENaC is associated in a macromolecular complex with Apx and alpha-spectrin in A6 cells and suggest that Apx is required for the functional expression of ENaC in Xenopus epithelia.

Publisher Summary The chapter presents a discussion on the mechanisms, whereby intracellular cyclic adenosine monophosphate (cAMP) increases amiloride-sensitive sodium ion (Na + ) channel activity. In some tissues, such as the rat distal colon and human nasal epithelia amiloride-sensitive Na + channel activity is not stimulated by CAMP. The peptide hormone vasopressin and its analogs, vasotocin and oxytocin, increase amiloride-sensitive Na + transport across mammalian collecting ducts and amphibian epithelia (that is, toad urinary bladder, frog skin and colon, and Xenopus A6 renal epithelial cells) two- to fourfold through an increase in intracellular cAMP. This increase in Na + transport develops rapidly over a period of 5–30 minutes and is initiated by the binding of vasopressin to V 2 receptors situated in the basolateral membrane. This in turn leads to the stimulation of adenylate cyclase via the heterotrimeric G protein, Gα s , and a concomitant increase in intracellular cAMP, which results in increased Na + channel activity. The fact that membrane-permeable cAMP analogs, inhibitors of phosphodiesterase, and activators of adenylate cyclase, all mimic the vasopressin induced activation of amiloride sensitive Na + channels clearly indicates that the action of vasopressin is mediated by cAMP. The chapter summarizes the data supporting activation of quiescent channels through a protein kinase A (PKA) mediated phosphorylation of a channel subunit or an associated regulatory protein.

Publisher Summary This chapter discusses the role of the membrane cytoskeleton in regulating epithelial ion channel activity. The function of epithelial cells as selective permeability barriers between the transcellular and interstitial fluid compartments depends upon the establishment and maintenance of the polarized distribution of membrane-transport proteins and ion channels to specific membrane domains. For example, Na + reabsorption by the kidney requires the localization of specific transporters, such as the Na + –H + exchanger, Na'-dependent glucose, amino acid and phosphate co-transporters, and Na' channels, to the apical membrane domain and Na + ,K + -ATPase to the basolateral membrane domain. If these proteins are not segregated into different membrane domains, as can result from neoplastic growth or can occur in renal diseases such as ischemia or adult polycystic kidney disease, renal Na + transport would be significantly impaired, and such a compromise in polarity may ultimately lead to renal failure. The understanding of the role of the membrane cytoskeleton in the regulation of epithelial ion channels is just beginning. Work on epithelial Na + channels has revealed that epithelial ion channels can be directly associated with the spectrin-based membrane cytoskeleton.

A new and highly unusual species of Lachnum Retz (ascomycetes, Hyaloscyphaceae) is described from decaying leaves of Deschampsia caespitosa (L) Beauv. collected from Argyll, Scotland.

We have previously demonstrated that apical Na+ channels in A6 renal epithelial cells are associated with spectrin-based membrane cytoskeleton proteins and that the lateral mobility of these channels, as determined by fluorescence photobleach recovery (FPR) analysis, is severely restricted by this association (Smith et al., 1991. Proc. Natl. Acad. Sci. USA 88:6971-6975). Recent data indicate that the actin component of the cytoskeleton may play a role in modulating Na+ channel activity (Cantiello et al., 1991. Am. J. Physiol. 261:C882-C888); however, it is unknown if the Na+ channel's linkage to the spectrin-based membrane cytoskeleton is also involved in regulating channel activity. In this study, we have used FPR to examine if the linkage of the Na+ channels to the membrane cytoskeleton is a site for modulation of Na+ channel activity in filter grown A6 cells by vasopressin and aldosterone. We hypothesized that if the linkage of the Na+ channels to the membrane cytoskeleton is a site for regulation of Na+ channel activity by vasopressin and aldosterone, then hormone-mediated changes in either the membrane cytoskeleton or the affinity of the Na+ channel for the membrane cytoskeleton, should be reflected in changes in the lateral mobility and/or mobile fraction of Na+ channels on the cell surface. FPR revealed that although the rates of lateral mobility were not affected, there was a twofold increase in mobility fraction (f) of apical Na+ channels in aldosterone-treated (16 hr) monolayers (f = 32.31 +/- 5.42%) when compared to control (unstimulated) (f = 14.2 +/- 0.77%) and vasopressin-treated (20 min) (f = 12.7 +/- 2.4%) monolayers. The twofold increase in mobile fraction of Na+ channels corresponds to the average increase in Na+ transport in response to aldosterone in A6 cells. The aldosterone-induced increase in Na+ transport and mobile fraction can be inhibited by the methylation inhibitor, 3-deazaadenosine, consistent with the hypothesis that a methylation event is involved in aldosterone induced upregulation of Na+ transport. We propose that the membrane cytoskeleton is involved in the aldosterone-mediated activation of epithelial Na+ channels.

We have used polyclonal antibodies generated against purified bovine renal amiloride-sensitive Na+ channels to localize amiloride-sensitive Na+ channels within the lower intestine (colon and coprodeum) of the hen. These antibodies cross-reacted with two polypeptides exhibiting M(r)'s of 235 and 150 kDa on immunoblots of detergent-solubilized apical membrane fractions from both the colon and coprodeum. The apparent molecular masses of theses polypeptides are in agreement with the M(r)'s of 2 of the subunits of the renal high amiloride-affinity Na+ channel, namely the alpha and the beta (= amiloride binding) subunits. The cellular distribution of Na+ channels was determined by immunoperoxidase and indirect immunofluorescence cytochemical techniques. The apical (luminal) membrane and cytoplasm of villar principal cells in both colon and coprodeum exhibited immunoreactivity, whereas goblet cells were negative. Both principal and goblet cells of the crypts were also negative. We conclude that the amiloride-sensitive Na+ channels are localized to the principal cells of the intestinal villi and that these cells are responsible for intestinal Na+ absorption.

The development of the polychaete Sabellaria cementarium Moore, 1906 proceeds at 10–14 °C, as follows: 23 h, early trochophore with prototroch and apical tuft; 65 h, 1 pair of provisional setae; 3.5 days, feeding trochophore; 18 days, metatrochophore; 4 weeks, metatrochophore with tentacle buds; 5–6 weeks, nectochaeta competent to metamorphose; 6–8 weeks, settlement and metamorphosis. Larval behavior is described. Tube sand of adult sabellariids (S. cementarium, Phragmatopoma lapidosa, ldanthrysus ornamentatus) and beach sand induced metamorphosis. Larvae exhibit a low degree of substrate specificity in their settlement, but sand is essential. Metamorphosis involves a loss of provisional setae, anterior rotation of tentacles and opercular cirri, and reduction of episphere. Following these changes, the juvenile secretes a mucoid tube to which sand grains are attached. Metamorphosis is considered complete when the caudal appendage has formed; this occurs 7–10 days postsettlement. Juveniles were kept in the laboratory for 38 days. During this time, they develop three pairs of tentacles, lose all larval pigment, and form a second thoracic segment. Within the opercular crown, primary opercular paleae replace settling paleae.

The mitraria larva of 0. fusiformis possesses a pair of nephridi@ which are not typical polychaete larval protonephridia, rather they resemble the pore canal-hydro pore complex ofdeuterostome larvae. An ultrastructural analysis ofthe nephridium reveals a small body cavity, lined by monciciliated podocytes, which opens to the exterior by a monociliated nephridioduct. Extracellular matrix between podocyte pedicels forms the filtration surface and podocyte and nephridioduct cilia produce the pressure gradient driving filtration. Therefore, each nephridium is considered a giant protonephridium. Although this organization is unique to Owenia among the annelids, it is identical ultrastructurally to the hydropore, pore canal, and adjoining coelom ofdeuterostome larvae, which is also a nephndium. It is concluded that this cytological similarity between the nephridia ofthe mitraria and deuterostome larvae reflects a cellular homology which has a wide distribution and is oflimited usefulness in the recognition of relationships. The anatomical differences between them suggest they are, at best, serially homologous organs. Mitraria nephridia compare more favor ably to the typical protonephridia (head kidneys) of polychaete trochophores and larval protonephridia of phoronids. Data support the view that Owenia is primitive among the polychaetes and suggest that the mitraria nephridium represents the plesi omorphic design of protonephridium within the Polychaeta.

The development of the blood vascular system (BVS) in larvae of the polychaete (Sabellaria cementarium was studied by light and electron microscopy. BVS formation begins in the metatrochophore, concomitant with onset of segmentation, and all major vessels and sinuses of the BVS have formed by the nectochaeta stage. Blood vessels form de novo by a separation of apposing basal extracellular matrices (ECM) of adjacent myoepithelial peritoneal cell layers, and blood sinuses also form de novo by a separation of the basal ECM of peritoneal cells from the basal ECM of the gut epithelium. Blood vessels and sinuses are lined only by the ECM of overlying cell layers. Podocytes are present overlying lateral esophageal and ventro-lateral trunk blood vessels. The results support the blastocoel theory of Lang (1904) and the “segmentation hypothesis” and structural model of Ruppert and Carle (1983) which presents the BVS of triploblastic Metazoa as a developmental and evolutionary modification of the basal ECM of overlying cell layers and argues that the adaptive significance of the BVS is to bypass septal partitions with a fluid transport system.

The histology of the nectochaeta larva of the polychaete Sabellaria cementarium Moore and its changes during metamorphosis are described. The epidermis of the nectochaeta consists of five types of cells: locomotory, sensory, pigment, gland, and nonciliated. Setal sacs, containing provisional setae and settling paleae, are located on either side of the body. The muscle system consists of circular and longitudinal trunk muscles and a setal sac – esophageal muscle complex. The alimentary tract consists of an esophagus possessing three types of gland cells, a stomach composed of large vacuolated cells anteriorly and squamous cells containing lipid droplets posteriorly, and an intestine. The nervous system is composed of a cerebral ganglion, circumesophageal connectives, subesophageal ganglia, and paired ventral nerve cords. The blood vascular system consists of supraesophageal, lateral esophageal, dorsal and ventral blood vessels, and dorsal and ventral blood sinuses. Mucous glands are present in the episphere and pygidium and five types of gland cells are found in the parathoracic region. Metamorphosis of the nectochaeta into a sedentary, benthic juvenile involves the following morphological changes: atrophy of prototrochal cells, loss of provisional setae and regional histolysis within the setal sacs, loss of epispheral and pygidial mucous glands, discharge of parathoracic glands that form the mucoid tube, formation of a head coelom, enlargement of cerebral ganglion, histolysis of the setal sac – esophageal muscle complex, and hypertrophy and dissociation of the vacuolated stomach cells.

The presence of hemoglobin in tissues of a small number of species is puzzling when homologous tissues of closely related species do not possess hemoglobin. Several species of bivalve molluscs possess nervous systems with nerve hemoglobin (neurohemoglobin). These systems were compared to nervous systems from other bivalve molluscs without neurohemoglobin to determine ultrastructural and electrophysiological characteristics under normoxic conditions in an attempt to locate any differences between these two types of nervous systems. Cerebro-visceral connectives from the bivalves Tellina alternata and Spisula solidissima with neurohemoglobin and Tagelus plebeius and Geukensia demissa without neurohemoglobin possess a perineural sheath, a subjacent peripheral layer of glial cells, and glial cell processes that enwrap bundles of 0.2-0.4 µm diameter axons. Neurohemoglobin-containing cerebro-visceral connectives have smaller axon bundles and more dense perineural sheaths than those without neurohemoglobin. These features may be important in oxygen delivery from the neurohemoglobin to the axons. Action potential traces, conduction velocities, refractory periods, strength-duration relationships, and temperature responses of all four connectives are typical of nerves possessing very small axons. There are no obvious electrophysiological differences between cerebro-visceral connectives with and without neurohemoglobin.

Summary (1) Based on the classical studies of Goodrich, protonephridia are believed to be phylogenetic antecedents of metanephridia. It is argued here that the primary factor determining the type of nephridium expressed is body size rather than phylogenetic status. (2) The proposed model defines a nephridium functionally and predicts two general configurations for filtration nephridia in animals. (3) Application of the model to metanephridial and protonephridial systems indicates differences in the sites of ultrafiltration and mechanisms of pressure generation. (4) Metanephridial systems function by muscle-mediated filtration of vascular fluid into a coelomic space before modification by an excretory duct. (5) Protonephridial systems function by cilia-mediated filtration of extracellular fluid into the lumen of a protonephridial terminal cell before modification in an adjoining duct. (6) The model predicts a correlation between animals with blood vessels and metanephridia, and animals without blood vessels and protonephridia. The correlation is shown to be nearly perfect. (7) Exceptions to the model are discussed. (8) Original experimental evidence is given for the permeability of the protonephridial terminal cell to iron dextran and its reabsorption by the protonephridial duct in the polychaete, Glycera dibranchiata. (9) Experimental data for proto- and metanephridial systems are summarized and shown to support the proposed model. (10) The ultrastructure of the exceptional amphioxus ‘protonephridium’ is reviewed and original data are presented. Its organization is structurally and perhaps functionally intermediate between proto- and metanephridial systems. (11) An original ultrastructural comparison is made of monociliated nitration cells in a size range of larval invertebrates from five phyla. Filtration cells that are structurally intermediate between protonephridial solenocytes and metanephridial podocytes are noted in larvae intermediate in body size between the two extremes. The comparative data suggest that (i) podocytes and solenocytes are homologous cells and (ii) that body size is correlated with which of the two designs is expressed. (12) The fates of larval podocytes are followed through metamorphosis in three species. The results confirm the equivalence of podocytes and solenocytes as suggested by the comparative analysis. They further indicate that which morph is expressed is a function of body design factors discussed in the model. (13) Protonephridia are believed to be primitive to metanephridia because they occur in presumably primitive animals and in ontogenetic stages of many animals with metanephridia as adults. It is suggested here that the distribution of protonephridia is related to small body size and the lack of blood vessels, regardless of phylogenetic status. The occurrence of protonephridia in the larvae of species with metanephridia as adults is explained similarly as a function of the small larval size and lack of blood vessels.

In immunohistochemical studies of rat liver tissue slices and purified nuclei, adenosine 3':5'-cyclic monophosphate (cAMP) and guanosine 3':5'-cyclic monophosphate (cGMP) immunofluorescence on the nuclear membrane are sequentially increased after glucagon administration. An explanation for the increased cGMP immunofluorescence was sought in experiments in which guanylate cyclase [GTP pyrophosphate-lyase (cyclizing), EC 4.6.1.2]activity of hepatic subcellular fractions was determined. The results showed that a nuclear guanylate cyclase exists which can be distinguished from the soluble and crude particulate guanylate cyclases. The activity of the nuclear enzyme was increased by 35% in nuclei isolated from rats 30 min after glucagon injection, the time at which maximal nuclear membrane cGMP immunofluorescence is observed. Because glucagon altered both cAMP location and levels prior to the observed changes in nuclear cGMP metabolism, the hypothesis that cAMP acted as the second messenger was tested. In vitro incubation of nuclei isolated from control rats with 10(-5) M cAMP produced a 25% increase in nuclear guanylate cyclase activity. With nuclei isolated from glucagon-treated rats, no significant increase in enzyme activity was observed; this indicates that maximal stimulation of nuclear guanylate cyclase by cAMP occurred at levels that are obtained in vivo after glucagon administration. These findings suggest that hepatic nuclear cGMP content may be regulated by a specific organelle guanylate cyclase and that cAMP may be one of the determinants of this enzyme's activity.