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Past work has shown that a subset of effector T cells with unique characteristics could abrogate hapten- or antigen-induced tolerance, and the reconstitution of this immune response has been termed contrasuppression. We have studied contrasuppression in a model of oral tolerance (OT) in which adoptively transferred antigen-specific T contrasuppressor (Tcs) cells reverse OT and result in antibody responses to the eliciting antigen. In the present study, we show that murine intraepithelial lymphocytes (IELs) from mice orally immunized with sheep red blood cells (SRBC) contain T cells that exhibit Tcs cell activity. This effect was mediated by CD3+ gamma/delta T cell receptor-positive (TCR+), but not alpha/beta TCR+ T cells, and gamma/delta TCR+ Tcs cells were associated with both the CD4-,CD8+ and CD4-,CD8- (double-negative) IEL fractions. The CD4-,CD8+ gamma/delta TCR+ IELs were further separated into Vicia villosa-adherent and -nonadherent fractions. Adoptive transfer of V. villosa-adherent gamma/delta TCR+ T cells to mice with OT to SRBC resulted in splenic IgA, IgM, and IgG subclass anti-SRBC responses, while V. villosa-nonadherent gamma/delta TCR+ T cells were without activity. The gamma/delta TCR+ IELs did not support in vitro antibody responses in B cell cultures, while alpha/beta TCR+ IELs were effective T helper cells. Further, cytokine production by the gamma/delta TCR+ IELs was examined, and the gamma/delta TCR+ V. villosa-adherent fraction, which possessed contrasuppressor function, contained low levels of IL-5 mRNA and small numbers of IL-5-producing cells when compared with alpha/beta TCR+ IELs and V. villosa-nonadherent gamma/delta TCR+ IELs. Our results now show that mouse IELs contain two distinct types of T cells that function in the immune response, e.g., alpha/beta TCR+ T cells that produce IL-5 and function as helper cells, and gamma/delta TCR+ T cells that restore antibody responses in mice that had been orally tolerized with antigen.

Procedures introduced here make it possible, first, to show that background (piecemeal) extinction is recorded throughout geologic stages and substages (not all extinction has occurred suddenly at the ends of such intervals); second, to separate out background extinction from mass extinction for a major crisis in earth history; and third, to correct for clustering of extinctions when using the rarefaction method to estimate the percentage of species lost in a mass extinction. Also presented here is a method for estimating the magnitude of the Signor-Lipps effect, which is the incorrect assignment of extinctions that occurred during a crisis to an interval preceding the crisis because of the incompleteness of the fossil record. Estimates for the magnitudes of mass extinctions presented here are in most cases lower than those previously published. They indicate that only ~81% of marine species died out in the great terminal Permian crisis, whereas levels of 90-96% have frequently been quoted in the literature. Calculations of the latter numbers were incorrectly based on combined data for the Middle and Late Permian mass extinctions. About 90 orders and more than 220 families of marine animals survived the terminal Permian crisis, and they embodied an enormous amount of morphological, physiological, and ecological diversity. Life did not nearly disappear at the end of the Permian, as has often been claimed. [ABSTRACT FROM AUTHOR]

We propose a new ecological ranking of the major Phanerozoic biodiversity crises in which the Serpukhovian biodiversity crisis is ranked fifth in ecological impact, lesser than the Late Devonian but greater than the end-Ordovician, and the end-Ordovician mass extinction is ranked sixth. It is interesting that both the end-Ordovician mass extinction and the Serpukhovian biodiversity crisis were triggered by glaciations. Other than that common trigger, the two events were very different. Glaciation in the Ordovician triggered an enormous jump in the extinction rate of marine organisms and was taxonomically very severe, yet the ecological impact of those extinctions was minimal. Glaciation in the Serpukhovian triggered a precipitous drop in the speciation rate but only moderate diversity losses, yet the ecological impact of those diversity losses and ecosystem restructuring was an ecological level of magnitude larger than that seen in the end-Ordovician mass extinction. [ABSTRACT FROM AUTHOR]

A geometric analysis of lophophore shape and arrangement in the fenestrate dendroid graptolite genus Dictyonema reveals that the shape of the zooid domain in the majority of Dictyonema species colonies is highly elliptical, with the long axis of the ellipse perpendicular to the proximodistal axis of the stipe. A complex lophophore, bilaterally symmetrical and consisting of two tentaculated arms that are laterally directed and perpendicular to the stipe axis, provides the best geometric solution to completely filling the elliptical zooid domain seen in the majority of Dictyonema species. Working under the assumption that fenestrate graptolites, like fenestrate bryozoans, needed to form a continuous filtering surface with contact between adjacent lophophores, two optimum close-parking models exist for lophophores with elliptical zooid domains: either a proximodistal-row arrangement or a lateral-row arrangement of the lophophores. Of the two possible geometries, the most probable close-packing arrangement of hypothetical biplumed lophophores within the fenestrate graptolite meshwork is in proximodistal rows. [ABSTRACT FROM AUTHOR]

Oral administration of large doses of protein antigen generally induces a state of systemic unresponsiveness currently termed mucosally induced tolerance. In this study, we used human milk protein (HMP) without casein as a multi-protein antigen for the study of mucosally induced tolerance. The HMP utilized in this study mainly contained secretory (S) IgA, lactoferrin (LO and a-lactalbumin (Lact). When mice were given 1 or 25 mg of HMP orally 3 times or 25 mg orally four consecutive weeks prior to systemic immunization, antigen-specific serum IgG responses to HMP were induced by subsequent parenteral immunization with 100 μg of HMP. Analysis of IgG subclasses revealed that IgG1 followed by IgG2b accounted for the IgG responses noted. When both HMP and ovalbumin (OVA) were fed to mice, tolerance developed to OVA but not to HMP. To further investigate the nature of immune responses seen following oral gavage of HMP, we examined responses to individual protein of HMP. Brisk serum IgG1 and IgG2b responses to both S-IgA and Lf were induced by oral followed by systemic immunization with HMP. Analysis of splenic CD4+ T cells from mice given oral HMP revealed production of Th2- but not Thl-type cytokines. These results show that oral administration of HMP preferentially induces exclusive Th2-type immune responses, which may prevent the development of HMP (S-IgA and Lf)-specific mucosally induced tolerance. [ABSTRACT FROM PUBLISHER]

The article presents the material of geometric models as an addendum to the research published in the March 2003 issue of the periodical "Journal of Paleontology." The said models will allow other researchers to assess the geometry of lophophore shapes and arrangements in the construction of such extinct modular organisms.