17 results on '"Attout, Tarik"'
Search Results
2. Mast cells aggravate sepsis by inhibiting peritoneal macrophage phagocytosis
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Dahdah, Albert, Gautier, Gregory, Attout, Tarik, Fiore, Frederic, Msallam, Emeline Lebourdais Rasha, Daeron, Marc, Monteiro, Renato C., Benhamou, Marc, Charles, Nicolas, Davoust, Jean, Blank, Ulrich, Malissen, Bernard, and Launay, Pierre
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Sepsis -- Development and progression -- Genetic aspects ,Mast cells -- Properties ,Macrophages -- Genetic aspects ,Phagocytosis -- Genetic aspects ,Health care industry - Abstract
Controlling the overwhelming inflammatory reaction associated with polymicrobial sepsis remains a prevalent clinical challenge with few treatment options. In septic peritonitis, blood neutrophils and monocytes are rapidly recruited into the peritoneal cavity to control infection, but the role of resident sentinel cells during the early phase of infection is less clear. In particular, the influence of mast cells on other tissue-resident cells remains poorly understood. Here, we developed a mouse model that allows both visualization and conditional ablation of mast cells and basophils to investigate the role of mast cells in severe septic peritonitis. Specific depletion of mast cells led to increased survival rates in mice with acute sepsis. Furthermore, we determined that mast cells impair the phagocytic action of resident macrophages, thereby allowing local and systemic bacterial proliferation. Mast cells did not influence local recruitment of neutrophils and monocytes or the release of inflammatory cytokines. Phagocytosis inhibition by mast cells involved their ability to release prestored IL-4 within 15 minutes after bacterial encounter, and treatment with an IL-4 -neutralizing antibody prevented this inhibitory effect and improved survival of septic mice. Our study uncovers a local crosstalk between mast cells and macrophages during the early phase of sepsis development that aggravates the outcome of severe bacterial infection., Introduction Sepsis is a life-threatening condition described as a syndrome of infection complicated by acute organ dysfunction. It is still a leading cause of death in intensive care units despite [...]
- Published
- 2014
- Full Text
- View/download PDF
3. Mast cells in renal inflammation and fibrosis: Lessons learnt from animal studies
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Madjene, Lydia Celia, Pons, Maguelonne, Danelli, Luca, Claver, Julien, Ali, Liza, Madera-Salcedo, Iris K., Kassas, Asma, Pellefigues, Christophe, Marquet, Florian, Dadah, Albert, Attout, Tarik, El-Ghoneimi, Alaa, Gautier, Gregory, Benhamou, Marc, Charles, Nicolas, Daugas, Eric, Launay, Pierre, and Blank, Ulrich
- Published
- 2015
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- View/download PDF
4. Increased early local immune responses and altered worm development in high-dose infections of mice susceptible to the filaria Litomosoides sigmodontis
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Babayan, Simon, Attout, Tarik, Specht, Sabine, Hoerauf, Achim, Snounou, Georges, Rénia, Laurent, Korenaga, Masataka, Bain, Odile, and Martin, Coralie
- Published
- 2005
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5. Vaccination against filarial nematodes with irradiated larvae provides long-term protection against the third larval stage but not against subsequent life cycle stages
- Author
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Babayan, Simon A., Attout, Tarik, Harris, Anjanette, Taylor, Matthew D., Le Goff, Laetitia, Vuong, Phat. N., Rénia, Laurent, Allen, Judith E., and Bain, Odile
- Published
- 2006
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6. CD47 agonist peptides induce programmed cell death in refractory chronic lymphocytic leukemia B cells via PLC[gamma]1 activation: evidence from mice and humans
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Martinez-Torres, Ana-Carolina, Quiney, Claire, Attout, Tarik, Boullet, Heloise, Herbi, Linda, Vela, Laura, Barbier, Sandrine, Chateau, Danielle, Chapiro, Elise, Nguyen-Khac, Florence, Davi, Frederic, Le Garff-Tavernier, Magali, Moumne, Roba, Sarfati, Marika, Karoyan, Philippe, Merle-Beral, Helene, Launay, Pierre, and Susin, Santos A.
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B cells -- Health aspects ,Phospholipases -- Health aspects ,Peptides -- Health aspects ,Cell death -- Identification and classification ,Chronic lymphocytic leukemia -- Physiological aspects ,Biological sciences - Abstract
Background Chronic lymphocytic leukemia (CLL), the most common adulthood leukemia, is characterized by the accumulation of abnormal [CD5.sup.+] B lymphocytes, which results in a progressive failure of the immune system. Despite intense research efforts, drug resistance remains a major cause of treatment failure in CLL, particularly in patients with dysfunctional TP53. The objective of our work was to identify potential approaches that might overcome CLL drug refractoriness by examining the pro-apoptotic potential of targeting the cell surface receptor CD47 with serum-stable agonist peptides. Methods and Findings In peripheral blood samples collected from 80 patients with CLL with positive and adverse prognostic features, we performed in vitro genetic and molecular analyses that demonstrate that the targeting of CD47 with peptides derived from the C-terminal domain of thrombospondin-1 efficiently kills the malignant CLL B cells, including those from high-risk individuals with a dysfunctional TP53 gene, while sparing the normal T and B lymphocytes from the CLL patients. Further studies reveal that the differential response of normal B lymphocytes, collected from 20 healthy donors, and leukemic B cells to CD47 peptide targeting results from the sustained activation in CLL B cells of phospholipase C gamma-1 (PLC[gamma]1), a protein that is significantly over-expressed in CLL. Once phosphorylated at tyrosine 783, PLC[gamma]1 enables a [Ca.sup.2+]-mediated, caspase-independent programmed cell death (PCD) pathway that is not down-modulated by the lymphocyte microenvironment. Accordingly, down-regulation of PLC[gamma]1 or pharmacological inhibition of PLC[gamma]1 phosphorylation abolishes CD47-mediated killing. Additionally, in a CLL-xenograft model developed in NOD/scid gamma mice, we demonstrate that the injection of CD47 agonist peptides reduces tumor burden without inducing anemia or toxicity in blood, liver, or kidney. The limitations of our study are mainly linked to the affinity of the peptides targeting CD47, which might be improved to reach the standard requirements in drug development, and the lack of a CLL animal model that fully mimics the human disease. Conclusions Our work provides substantial progress in (i) the development of serum-stable CD47 agonist peptides that are highly effective at inducing PCD in CLL, (ii) the understanding of the molecular events regulating a novel PCD pathway that overcomes CLL apoptotic avoidance, (iii) the identification of PLC[gamma]1 as an over-expressed protein in CLL B cells, and (iv) the description of a novel peptide-based strategy against CLL., Introduction Chronic lymphocytic leukemia (CLL), a human malignancy caused by an imbalance between proliferation and programmed cell death (PCD) [1], is the most common form of leukemia in adults. CLL [...]
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- 2015
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7. Visualizing Non Infectious and Infectious Anopheles gambiae Blood Feedings in Naive and Saliva-Immunized Mice.
- Author
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Choumet, Valerie, Attout, Tarik, Chartier, Loïc, Khun, Huot, Sautereau, Jean, Robbe-Vincent, Annie, Brey, Paul, Huerre, Michel, and Bain, Odile
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ANOPHELES gambiae , *BLOOD , *SALIVA , *LABORATORY mice , *SKIN , *FILARIASIS - Abstract
Background: Anopheles gambiae is a major vector of malaria and lymphatic filariasis. The arthropod-host interactions occurring at the skin interface are complex and dynamic. We used a global approach to describe the interaction between the mosquito (infected or uninfected) and the skin of mammals during blood feeding. Methods: Intravital video microscopy was used to characterize several features during blood feeding. The deposition and movement of Plasmodium berghei sporozoites in the dermis were also observed. We also used histological techniques to analyze the impact of infected and uninfected feedings on the skin cell response in naive mice. Results: The mouthparts were highly mobile within the skin during the probing phase. Probing time increased with mosquito age, with possible effects on pathogen transmission. Repletion was achieved by capillary feeding. The presence of sporozoites in the salivary glands modified the behavior of the mosquitoes, with infected females tending to probe more than uninfected females (86% versus 44%). A white area around the tip of the proboscis was observed when the mosquitoes fed on blood from the vessels of mice immunized with saliva. Mosquito feedings elicited an acute inflammatory response in naive mice that peaked three hours after the bite. Polynuclear and mast cells were associated with saliva deposits. We describe the first visualization of saliva in the skin by immunohistochemistry (IHC) with antibodies directed against saliva. Both saliva deposits and sporozoites were detected in the skin for up to 18 h after the bite. Conclusion: This study, in which we visualized the probing and engorgement phases of Anopheles gambiae blood meals, provides precise information about the behavior of the insect as a function of its infection status and the presence or absence of anti-saliva antibodies. It also provides insight into the possible consequences of the inflammatory reaction for blood feeding and pathogen transmission. [ABSTRACT FROM AUTHOR]
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- 2012
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8. The Chemokine CXCL12 Is Essential for the Clearance of the Filaria Litomosoides sigmodontis in Resistant Mice.
- Author
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Bouchery, Tiffany, Dénécé, Gaelle, Attout, Tarik, Ehrhardt, Katharina, Lhermitte-Vallarino, Nathaly, Hachet-Haas, Muriel, Galzi, Jean Luc, Brotin, Emilie, Bachelerie, Françoise, Gavotte, Laurent, Moulia, Catherine, Bain, Odile, and Martin, Coralie
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RAT diseases ,LITOMOSOIDES ,SKIN ,CHEMOKINES ,PARASITES ,CELLS - Abstract
Litomosoides sigmodontis is a cause of filarial infection in rodents. Once infective larvae overcome the skin barrier, they enter the lymphatic system and then settle in the pleural cavity, causing soft tissue infection. The outcome of infection depends on the parasite's modulatory ability and also on the immune response of the infected host, which is influenced by its genetic background. The goal of this study was to determine whether host factors such as the chemokine axis CXCL12/ CXCR4, which notably participates in the control of immune surveillance, can influence the outcome of the infection. We therefore set up comparative analyses of subcutaneous infection by L. sigmodontis in two inbred mouse strains with different outcomes: one susceptible strain (BALB/c) and one resistant strain (C57BL/6). We showed that rapid parasite clearance was associated with a L. sigmodontis-specific CXCL12-dependent cell response in C57BL/6 mice. CXCL12 was produced mainly by pleural mesothelial cells during infection. Conversely, the delayed parasite clearance in BALB/c mice was neither associated with an increase in CXCL12 levels nor with cell influx into the pleural cavity. Remarkably, interfering with the CXCL12/CXCR4 axis in both strains of mice delayed filarial development, as evidenced by the postponement of the fourth molting process. Furthermore, the in vitro growth of stage 4 filariae was favored by the addition of low amounts of CXCL12. The CXCL12/CXCR4 axis thus appears to have a dual effect on the L. sigmodontis life cycle: by acting as a host-cell restriction factor for infection, and as a growth factor for worms. [ABSTRACT FROM AUTHOR]
- Published
- 2012
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9. Lymphatic Vascularisation and Involvement of Lyve-1+ Macrophages in the Human Onchocerca Nodule.
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Attout, Tarik, Hoerauf, Achim, Dénécé, Gaëlle, Debrah, Alexander Yaw, Marfo-Debrekyei, Yeboah, Boussinesq, Michel, Wanji, Samuel, Martinez, Valérie, Mand, Sabine, Adjei, Ohene, Bain, Odile, Specht, Sabine, and Martin, Coralie
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ONCHOCERCIASIS , *NEMATODES , *ONCHOCERCA volvulus , *SKIN diseases , *FILARIASIS , *NEOVASCULARIZATION , *BLOOD vessels - Abstract
Onchocerciasis, caused by the filarial nematode Onchocerca volvulus, is a parasitic disease leading to debilitating skin disease and blindness, with major economic and social consequences. The pathology of onchocerciasis is principally considered to be a consequence of long-standing host inflammatory responses. In onchocerciasis a subcutaneous nodule is formed around the female worms, the core of which is a dense infiltrate of inflammatory cells in which microfilariae are released. It has been established that the formation of nodules is associated with angiogenesis. In this study, we show using specific markers of endothelium (CD31) and lymphatic endothelial cells (Lyve-1, Podoplanin) that not only angiogenesis but also lymphangiogenesis occurs within the nodule. 7% of the microfilariae could be found within the lymphatics, but none within blood vessels in these nodules, suggesting a possible route of migration for the larvae. The neovascularisation was associated with a particular pattern of angio/lymphangiogenic factors in nodules of onchocerciasis patients, characterized by the expression of CXCL12, CXCR4, VEGF-C, Angiopoietin-1 and Angiopoietin-2. Interestingly, a proportion of macrophages were found to be positive for Lyve-1 and some were integrated into the endothelium of the lymphatic vessels, revealing their plasticity in the nodular micro-environment. These results indicate that lymphatic as well as blood vascularization is induced around O. volvulus worms, either by the parasite itself, e.g. by the release of angiogenic and lymphangiogenic factors, or by consecutive host immune responses. [ABSTRACT FROM AUTHOR]
- Published
- 2009
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10. Pleural cellular reaction to the filarial infection Litomosoides sigmodontis is determined by the moulting process, the worm alteration, and the host strain
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Attout, Tarik, Martin, Coralie, Babayan, Simon A., Kozek, Wieslaw J., Bazzocchi, Chiara, Oudet, François, Gallagher, Iain J., Specht, Sabine, and Bain, Odile
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GRANULOMA , *INFLAMMATION , *CHRONIC granulomatous disease , *RODENTS - Abstract
Abstract: The filarial nematode Litomosoides sigmodontis model was used to decipher the complex in vivo relationships between filariae, granulomas and leukocytes in the host''s pleural cavity. The study was performed from D5 p.i.: to D47 p.i. in resistant C57BL/6 mice, to D74 p.i. in susceptible BALB/c mice, and to D420 p.i. in permissive jirds. We showed that, during the first month, leukocytes only clustered as granulomas around shed cuticles (exuviae) and with eosinophils as the major constituents. In addition, carbohydrates residues became abundant on exuviae only, suggesting a glycan-dependent mechanism of eosinophil attachment. Neutrophils were absent from the pleural cavity of all rodents and from the murine granulomas, but they made up 25% of the granuloma cell population in jirds. After the first month of infection granulomas formed around developed adult worms and morphological evidence suggested that leukocytes preferentially clustered around altered, but still motile, worms. No carbohydrates were detected on these worms and neutrophils were abundant in those granulomas. Finally, a rare third type of granuloma was observed in the resistant mice only; they contained young newly moulted adult worms; typically these granulomas were attached to the lateral lines of the worm via eosinophils; this feature correlated with the persistence of carbohydrate residues on the worms'' lateral lines. Neutrophils were always in low proportion in all granulomas from resistant mice, suggesting difference in their adhesive properties in these mice. In vitro neutrophil recruitment in resistant mice was similar to that observed in susceptible mice although they expressed less cell surface CD11b. [Copyright &y& Elsevier]
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- 2008
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11. Increased early local immune responses and altered worm development in high-dose infections of mice susceptible to the filariaLitomosoides sigmodontis.
- Author
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Babayan, Simon, Attout, Tarik, Specht, Sabine, Hoerauf, Achim, Snounou, Georges, Rénia, Laurent, Korenaga, Masataka, Bain, Odile, and Martin, Coralie
- Subjects
IMMUNE response ,IMMUNOLOGY ,BLOOD plasma ,MICE ,LYMPH nodes ,SERUM - Abstract
The relationship between the number of larvae inoculated and filarial infection outcome is an important fundamental and epidemiological issue. Our study was carried out with BALB/c mice infected with the filariaLitomosoides sigmodontis. For the first time, an immunological analysis of infection with various doses was studied in parallel with parasitological data. Mice were inoculated with 200, 60 or 25 infective larvae (third stage larvae, L3), and monitored over 80 days. At 60 h post-inoculation the immune response was stronger in the 200 L3 group than the 25 L3 group. Cells from lymph nodes draining the site of inoculation proliferated intensely and produced large amounts of IL-5 and IL-4. In the pleural cavity, leukocyte populations accumulated earlier and in larger quantities. IgG1, IL-4 and IL-10 serum concentrations were transiently higher. During the first 10 days the worm recovery rates were identical in all groups, but decreased thereafter in the 200 L3 group. In this group, the development of the worms was altered, with reduced lengths, diminished intra-uterine production of microfilariae and abnormalities of male copulatory organs. Whereas mice inoculated with 25 L3 became microfilaraemic, only one third reached patency in the 200 L3 group. However, detrimental effects of high numbers of worms are not seen in studies using different inoculation protocols. This suggests that the very early events determine subsequent immune response and infection outcome rather than competitive interactions between the worms. [ABSTRACT FROM AUTHOR]
- Published
- 2005
- Full Text
- View/download PDF
12. The subcutaneous movements of filarial infective larvae are impaired in vaccinated hosts in comparison to primary infected hosts.
- Author
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Babayan, Simon A., Attout, Tarik, Vuong, Phat N., Le Goff, Laetitia, Gantier, Jean-Charles, and Bain, Odile
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FILARIAL worms , *LARVAE , *FILARIASIS , *ANIMAL models in research , *LITOMOSOIDES , *LEUCOCYTES - Abstract
Our aim in this study was to observe the movements of filarial infective larvae following inoculation into the mammalian host and to assess the effect of vaccination on larval migration, in situ. Here we present recordings of larvae progressing through the subcutaneous tissues and inguinal lymph node of primary infected or vaccinated mice. We used the filaria Litomosoides sigmodontis in BALB/c mice that were necropsied 6 hours after the challenge inoculation of 200 larvae. Subcutaneous tissue sections were taken from the inoculation site and larvae were filmed in order to quantify their movements. Our analyses showed that the subcutaneous larvae were less motile in the vaccinated mice than in primary-infected mice and had more leucocytes attached to the cuticle. We propose that this reduced motility may result in the failure of a majority of larvae to evade the inflammatory reaction, thereby being a possible mechanism involved in the early vaccine-induced protection. [ABSTRACT FROM AUTHOR]
- Published
- 2005
- Full Text
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13. Munc18-2 and Syntaxin 3 Control Distinct Essential Steps in Mast Cell Degranulation.
- Author
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Brochetta, Cristiana, Suzuki, Ryo, Vita, Francesca, Soranzo, Maria Rosa, Claver, Julien, Madjene, Lydia Celia, Attout, Tarik, Vitte, Joana, Varin-Blank, Nadine, Zabucchi, Giuliano, Rivera, Juan, and Blank, Ulrich
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SYNTAXINS , *MAST cells , *PROTEIN receptors , *MEMBRANE fusion , *SMALL interfering RNA , *CYTOPLASMIC granules , *CHEMOKINES - Abstract
Mast cell degranulation requires N-ethylmaleimide-sensitive factor attachment protein receptors (SNARE) and mammalian uncoordinated18 (Munc18) fusion accessory proteins for membrane fusion. However, it is still unknown how their interaction supports fusion. In this study, we found that small interfering RNA-mediated silencing of the isoform Munc18-2 in mast cells inhibits cytoplasmic secretory granule (SG) release but not CCL2 chemokine secretion. Silencing of its SNARE-binding partner syntaxin 3 (STX3) also markedly inhibited degranulation, whereas combined knockdown produced an additive inhibitory effect. Strikingly, while Munc18-2 silencing impaired SG translocation, silencing of STX3 inhibited fusion, demonstrating unique roles of each protein. Immunogold studies showed that both Munc18-2 and STX3 are located on the granule surface, but also within the granule matrix and in small nocodazole-sensitive clusters of the cytoskeletal meshwork surrounding SG. After stimulation, clusters containing both effectors were detected at fusion sites. In resting cells, Munc18-2, but not STX3, interacted with tubulin. This interaction was sensitive to nocodazole treatment and decreased after stimulation. Our results indicate that Munc18-2 dynamically couples the membrane fusion machinery to the microtubule cytoskeleton and demonstrate that Munc18-2 and STX3 perform distinct, but complementary, functions to support, respectively, SG translocation and membrane fusion in mast cells. [ABSTRACT FROM AUTHOR]
- Published
- 2014
- Full Text
- View/download PDF
14. The TRPM4 Channel Controls Monocyte and Macrophage, but Not Neutrophil, Function for Survival in Sepsis.
- Author
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Serafini, Nicolas, Dahdah, Albert, Barbet, Gaëtan, Demion, Marie, Attout, Tarik, Gautier, Grégory, Arcos-Fajardo, Michelle, Souche, Hervé, Jouvin, Marie-Hélène, Vrtovsnik, François, Kinet, Jean-Pierre, Benhamou, Marc, Monteiro, Renato C., and Launay, Pierre
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MONOCYTES , *MACROPHAGES , *NEUTROPHILS , *SEPSIS , *BACTERIAL diseases , *HEALTH outcome assessment - Abstract
A favorable outcome following acute bacterial infection depends on the ability of phagocytic cells to be recruited and properly activated within injured tissues. Calcium (Ca2+) is a ubiquitous second messenger implicated in the functions of many cells, but the mechanisms involved in the regulation of Ca2+ mobilization in hematopoietic cells are largely unknown. The monovalent cation channel transient receptor potential melastatin (TRPM) 4 is involved in the control of Ca2+ signaling in some hematopoietic cell types, but the role of this channel in phagocytes and its relevance in the control of inflammation remain unexplored. In this study, we report that the ablation of the Trpm4 gene dramatically increased mouse mortality in a model of sepsis induced by cecal ligation and puncture. The lack of the TRPM4 channel affected macrophage population within bacteria-infected peritoneal cavities and increased the systemic level of Ly6C+ monocytes and proinflammatory cytokine production. Impaired Ca2+ mobili-zation in Trpm4-/- macrophages downregulated the AKT signaling pathway and the subsequent phagocytic activity, resulting in bacterial overgrowth and translocation to the bloodstream. In contrast, no alteration in the distribution, function, or Ca2+ mobilization of Trpm4-/- neutrophils was observed, indicating that the mechanism controlling Ca2+ signaling differs among phagocytes. Our results thus show that the tight control of Ca2+ influx by the TRPM4 channel is critical for the proper functioning of monocytes/macrophages and the efficiency of the subsequent response to infection. [ABSTRACT FROM AUTHOR]
- Published
- 2012
- Full Text
- View/download PDF
15. Calcium channels in Fc receptor signaling.
- Author
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Attout T, Floto A, and Launay P
- Subjects
- Animals, Calcium metabolism, Calcium Signaling, Humans, Calcium Channels physiology, Receptors, Fc physiology, Signal Transduction physiology
- Abstract
The calcium ion (Ca(2+)) is the main common second messenger involved in signaling transduction subsequent to immunoreceptor activation. Its rapid intracellular elevation induces multiple cellular responses, such as secretion, proliferation, mobility, and gene transcription. Intracellular levels of Ca(2+) need to reach a specific threshold to efficiently transduce the signal to activate transcription factors through the recruitment of Ca(2+)-binding molecules. However, since Ca(2+) cannot be metabolized, its intracellular concentration is tightly regulated to avoid the induction of programmed cell death. This highly controlled regulation of Ca(2+) homeostasis has recently been clarified by the uncovering of new ion channels. The regulation of these channels allows the role of Ca(2+) in Fc receptor transduction pathways to be more precisely defined.
- Published
- 2014
- Full Text
- View/download PDF
16. Lymphatic vascularisation and involvement of Lyve-1+ macrophages in the human onchocerca nodule.
- Author
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Attout T, Hoerauf A, Dénécé G, Debrah AY, Marfo-Debrekyei Y, Boussinesq M, Wanji S, Martinez V, Mand S, Adjei O, Bain O, Specht S, and Martin C
- Subjects
- Angiogenesis Inducing Agents metabolism, Animals, Cell Movement, Dermis parasitology, Dermis pathology, Endothelium, Lymphatic metabolism, Endothelium, Lymphatic parasitology, Female, Humans, Lymphatic Vessels parasitology, Macrophages parasitology, Microfilariae cytology, Onchocerca volvulus cytology, Onchocerca volvulus physiology, Lymphatic Vessels blood supply, Macrophages metabolism, Onchocerciasis parasitology, Onchocerciasis pathology, Vesicular Transport Proteins metabolism
- Abstract
Onchocerciasis, caused by the filarial nematode Onchocerca volvulus, is a parasitic disease leading to debilitating skin disease and blindness, with major economic and social consequences. The pathology of onchocerciasis is principally considered to be a consequence of long-standing host inflammatory responses. In onchocerciasis a subcutaneous nodule is formed around the female worms, the core of which is a dense infiltrate of inflammatory cells in which microfilariae are released. It has been established that the formation of nodules is associated with angiogenesis. In this study, we show using specific markers of endothelium (CD31) and lymphatic endothelial cells (Lyve-1, Podoplanin) that not only angiogenesis but also lymphangiogenesis occurs within the nodule. 7% of the microfilariae could be found within the lymphatics, but none within blood vessels in these nodules, suggesting a possible route of migration for the larvae. The neovascularisation was associated with a particular pattern of angio/lymphangiogenic factors in nodules of onchocerciasis patients, characterized by the expression of CXCL12, CXCR4, VEGF-C, Angiopoietin-1 and Angiopoietin-2. Interestingly, a proportion of macrophages were found to be positive for Lyve-1 and some were integrated into the endothelium of the lymphatic vessels, revealing their plasticity in the nodular micro-environment. These results indicate that lymphatic as well as blood vascularization is induced around O. volvulus worms, either by the parasite itself, e.g. by the release of angiogenic and lymphangiogenic factors, or by consecutive host immune responses.
- Published
- 2009
- Full Text
- View/download PDF
17. Resistance and susceptibility to filarial infection with Litomosoides sigmodontis are associated with early differences in parasite development and in localized immune reactions.
- Author
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Babayan S, Ungeheuer MN, Martin C, Attout T, Belnoue E, Snounou G, Rénia L, Korenaga M, and Bain O
- Subjects
- Animals, Antibodies, Helminth blood, Female, Filariasis parasitology, Filariasis physiopathology, Filarioidea immunology, Larva growth & development, Larva immunology, Larva pathogenicity, Lymph Nodes parasitology, Male, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Pleural Cavity parasitology, Species Specificity, Cytokines biosynthesis, Disease Susceptibility, Filariasis immunology, Filarioidea growth & development, Filarioidea pathogenicity, Lymph Nodes immunology, Pleural Cavity immunology
- Abstract
In order to understand natural resistance to filariasis, we compared Litomosoides sigmodontis primary infection of C57BL/6 mice, which eliminate the worms before patency, and BALB/c mice, in which worms complete their development and produce microfilariae. Our analysis over the first month of infection monitoredmigration of the infective larvae from the lymph nodes to the pleural cavity, where the worms settle. Although immune responses from the mouse strains differed from the outset, the duration of lymphatic migration (4 days) and filarial recovery rates were similar, thus confirming that the proportion of larvae that develop in the host species upon infection is not influenced by host genetic variability. The majority of worms reached the adult stage in both mouse strains; however, worm growth and molting were retarded in resistant C57BL/6 mice. Surprisingly, the only immune responses detected at 60 h postinfection occurred in the susceptible mice and only upon stimulation of cells from lymph nodes draining the inoculation site with infective larva extract: massive production of interleukin-6 (IL-6) and IL-5 (the latter cytokine was previously suspected to have an effect on L. sigmodontis growth). However, between days 10 and 30 postinfection, extraordinarily high levels of type 1 and type 2 cytokines and expansion of pleural leukocyte infiltration were seen in the resistant C57BL/6 mice, explaining the destruction of worms later. Our results suggest that events early in the infection determine susceptibility or resistance to subsequent microfilarial production and a parasite strategy to use specific immune responses to its own benefit.
- Published
- 2003
- Full Text
- View/download PDF
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