ATP-Gated Ionotropic P2X7 Receptor Controls Follicular T Helper Cell Numbers in Peyer’s Patches to Promote Host-Microbiota Mutualism

Microbial colonization of the gut induces the development of gut-associated lymphoid tissue (GALT). The molecular mechanisms that regulate GALT function and result in gut-commensal homeostasis are poorly defined. T follicular helper (Tfh) cells in Peyer’s patches (PPs) promote high-affinity IgA resp...

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Published inImmunity (Cambridge, Mass.) Vol. 41; no. 5; pp. 789 - 801
Main Authors Proietti, Michele, Cornacchione, Vanessa, Rezzonico Jost, Tanja, Romagnani, Andrea, Faliti, Caterina Elisa, Perruzza, Lisa, Rigoni, Rosita, Radaelli, Enrico, Caprioli, Flavio, Preziuso, Silvia, Brannetti, Barbara, Thelen, Marcus, McCoy, Kathy D., Slack, Emma, Traggiai, Elisabetta, Grassi, Fabio
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 20.11.2014
Elsevier Limited
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Abstract Microbial colonization of the gut induces the development of gut-associated lymphoid tissue (GALT). The molecular mechanisms that regulate GALT function and result in gut-commensal homeostasis are poorly defined. T follicular helper (Tfh) cells in Peyer’s patches (PPs) promote high-affinity IgA responses. Here we found that the ATP-gated ionotropic P2X7 receptor controls Tfh cell numbers in PPs. Lack of P2X7 in Tfh cells enhanced germinal center reactions and high-affinity IgA secretion and binding to commensals. The ensuing depletion of mucosal bacteria resulted in reduced systemic translocation of microbial components, lowering B1 cell stimulation and serum IgM concentrations. Mice lacking P2X7 had increased susceptibility to polymicrobial sepsis, which was rescued by Tfh cell depletion or administration of purified IgM. Thus, regulation of Tfh cells by P2X7 activity is important for mucosal colonization, which in turn results in IgM serum concentrations necessary to protect the host from bacteremia. [Display omitted] •P2X7 receptor controls T-cell-dependent IgA response to preserve commensalism•Lack of P2X7 receptor results in commensal depletion and reduced serum IgM•Mice lacking P2X7 receptor have increased susceptibility to polymicrobial sepsis•Purinergic control of Tfh cell help to B cells is conserved in humans T follicular helper (Tfh) cells in Peyer’s patches promote high-affinity IgA responses, which ensure mucosal protection. Grassi and colleagues demonstrate that P2X7 receptor-mediated regulation of Tfh cells allows mucosal colonization and controlled translocation of microbial components that stimulate systemic IgM and protect the host from bacteremia.
AbstractList Microbial colonization of the gut induces the development of gut-associated lymphoid tissue (GALT). The molecular mechanisms that regulate GALT function and result in gut-commensal homeostasis are poorly defined. T follicular helper (Tfh) cells in Peyer's patches (PPs) promote high-affinity IgA responses. Here we found that the ATP-gated ionotropic P2X7 receptor controls Tfh cell numbers in PPs. Lack of P2X7 in Tfh cells enhanced germinal center reactions and high-affinity IgA secretion and binding to commensals. The ensuing depletion of mucosal bacteria resulted in reduced systemic translocation of microbial components, lowering B1 cell stimulation and serum IgM concentrations. Mice lacking P2X7 had increased susceptibility to polymicrobial sepsis, which was rescued by Tfh cell depletion or administration of purified IgM. Thus, regulation of Tfh cells by P2X7 activity is important for mucosal colonization, which in turn results in IgM serum concentrations necessary to protect the host from bacteremia.Microbial colonization of the gut induces the development of gut-associated lymphoid tissue (GALT). The molecular mechanisms that regulate GALT function and result in gut-commensal homeostasis are poorly defined. T follicular helper (Tfh) cells in Peyer's patches (PPs) promote high-affinity IgA responses. Here we found that the ATP-gated ionotropic P2X7 receptor controls Tfh cell numbers in PPs. Lack of P2X7 in Tfh cells enhanced germinal center reactions and high-affinity IgA secretion and binding to commensals. The ensuing depletion of mucosal bacteria resulted in reduced systemic translocation of microbial components, lowering B1 cell stimulation and serum IgM concentrations. Mice lacking P2X7 had increased susceptibility to polymicrobial sepsis, which was rescued by Tfh cell depletion or administration of purified IgM. Thus, regulation of Tfh cells by P2X7 activity is important for mucosal colonization, which in turn results in IgM serum concentrations necessary to protect the host from bacteremia.
Microbial colonization of the gut induces the development of gut-associated lymphoid tissue (GALT). The molecular mechanisms that regulate GALT function and result in gut-commensal homeostasis are poorly defined. T follicular helper (Tfh) cells in Peyer's patches (PPs) promote high-affinity IgA responses. Here we found that the ATP-gated ionotropic P2X7 receptor controls Tfh cell numbers in PPs. Lack of P2X7 in Tfh cells enhanced germinal center reactions and high-affinity IgA secretion and binding to commensals. The ensuing depletion of mucosal bacteria resulted in reduced systemic translocation of microbial components, lowering B1 cell stimulation and serum IgM concentrations. Mice lacking P2X7 had increased susceptibility to polymicrobial sepsis, which was rescued by Tfh cell depletion or administration of purified IgM. Thus, regulation of Tfh cells by P2X7 activity is important for mucosal colonization, which in turn results in IgM serum concentrations necessary to protect the host from bacteremia.
Microbial colonization of the gut induces the development of gut-associated lymphoid tissue (GALT). The molecular mechanisms that regulate GALT function and result in gut-commensal homeostasis are poorly defined. T follicular helper (Tfh) cells in Peyer’s patches (PPs) promote high-affinity IgA responses. Here we found that the ATP-gated ionotropic P2X7 receptor controls Tfh cell numbers in PPs. Lack of P2X7 in Tfh cells enhanced germinal center reactions and high-affinity IgA secretion and binding to commensals. The ensuing depletion of mucosal bacteria resulted in reduced systemic translocation of microbial components, lowering B1 cell stimulation and serum IgM concentrations. Mice lacking P2X7 had increased susceptibility to polymicrobial sepsis, which was rescued by Tfh cell depletion or administration of purified IgM. Thus, regulation of Tfh cells by P2X7 activity is important for mucosal colonization, which in turn results in IgM serum concentrations necessary to protect the host from bacteremia. [Display omitted] •P2X7 receptor controls T-cell-dependent IgA response to preserve commensalism•Lack of P2X7 receptor results in commensal depletion and reduced serum IgM•Mice lacking P2X7 receptor have increased susceptibility to polymicrobial sepsis•Purinergic control of Tfh cell help to B cells is conserved in humans T follicular helper (Tfh) cells in Peyer’s patches promote high-affinity IgA responses, which ensure mucosal protection. Grassi and colleagues demonstrate that P2X7 receptor-mediated regulation of Tfh cells allows mucosal colonization and controlled translocation of microbial components that stimulate systemic IgM and protect the host from bacteremia.
Author Grassi, Fabio
Faliti, Caterina Elisa
Proietti, Michele
Perruzza, Lisa
Traggiai, Elisabetta
Rigoni, Rosita
Caprioli, Flavio
Preziuso, Silvia
Radaelli, Enrico
Brannetti, Barbara
McCoy, Kathy D.
Rezzonico Jost, Tanja
Slack, Emma
Romagnani, Andrea
Cornacchione, Vanessa
Thelen, Marcus
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  surname: Preziuso
  fullname: Preziuso, Silvia
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  surname: McCoy
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Snippet Microbial colonization of the gut induces the development of gut-associated lymphoid tissue (GALT). The molecular mechanisms that regulate GALT function and...
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SubjectTerms Adenosine Triphosphate - metabolism
Age
Animals
Apoptosis
B-Lymphocytes - immunology
Bacteremia - immunology
Biomedical research
Experiments
Flow cytometry
Genetic Predisposition to Disease
Germinal Center - immunology
Humans
Immune system
Immunoglobulin A - immunology
Immunoglobulin M - blood
Intestinal Mucosa - immunology
Intestinal Mucosa - microbiology
Lymphocyte Depletion
Lymphocytes
Mice
Mice, Inbred C57BL
Mice, Knockout
Microbiota - immunology
Mothers
Peyer's Patches - cytology
Peyer's Patches - immunology
Physiology
Receptors, Purinergic P2X7 - genetics
Receptors, Purinergic P2X7 - immunology
Rodents
Sepsis - immunology
Sepsis - microbiology
Symbiosis - immunology
T-Lymphocytes, Helper-Inducer - immunology
Title ATP-Gated Ionotropic P2X7 Receptor Controls Follicular T Helper Cell Numbers in Peyer’s Patches to Promote Host-Microbiota Mutualism
URI https://dx.doi.org/10.1016/j.immuni.2014.10.010
https://www.ncbi.nlm.nih.gov/pubmed/25464855
https://www.proquest.com/docview/1626716515
https://www.proquest.com/docview/1635030297
https://www.proquest.com/docview/1639972468
Volume 41
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