B1 B cells acquire a proliferative and anti-inflammatory profile during pregnancy in mice

Autores
Valeff, Natalin Jimena; Abba, Martin C.; Jensen, Federico
Año de publicación
2021
Idioma
inglés
Tipo de recurso
documento de conferencia
Estado
versión publicada
Descripción
B1 B cells are a distinct subpopulation of B cells characterized by their unique capacity of self-renewal and the ability to secrete IgM without foreign antigen exposure (natural antibodies). In addition, upon activation, B1 B cells produce large quantities of the potent anti-inflammatory cytokine IL-10. Though the mechanisms that control natural antibodies production are not fully elucidated, it was recently associated with a down-regulation of CD1d expression in B1 B cells. Taking into account that both, IL-10 and natural antibodies are known to be fundamental components in pregnancy wellbeing, the aim of this study was to evaluate proliferation status as well as CD1d expression and IL-10 production by B1 B cells during pregnancy. Flow cytometry analysis, on splenic B1 B cells from pregnant (P) and non-pregnant (NP) mice was performed to evaluate ki-67 (proliferation marker) and CD1d expression as well as IL-10 production upon LPS stimulation. We observed significantly higher expression levels of Ki-67 in splenic B1 B cells from P compared to NP (Unpaired t-test p<0,0001; n=3) mice which was mirrored by higher percentages of B1 B cells in the spleen of P mice (Unpaired t-test p=0,0095; n=11). In addition, B1 B cells from P mice expressed lower levels of CD1d as compared to NP mice (Unpaired t-test p<0,0001; n=3). Furthermore, LPS-stimulated B1 B cells from P mice produced significantly higher levels of IL-10 compared to NP mice in vitro (Unpaired t-test p=0,015; n=5).Overall, our results demonstrate that not only B1 B cells are expanded in the spleen during pregnancy but they also seem to acquire the capacity to produce higher levels of natural antibodies and IL-10 during this period, suggesting their critical role in the intricate process of pregnancy tolerance.
Fil: Valeff, Natalin Jimena. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Centro de Estudios Farmacológicos y Botánicos. Universidad de Buenos Aires. Facultad de Medicina. Centro de Estudios Farmacológicos y Botánicos; Argentina
Fil: Abba, Martin C.. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Centro de Investigaciones Inmunológicas Básicas y Aplicadas; Argentina
Fil: Jensen, Federico. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Centro de Estudios Farmacológicos y Botánicos. Universidad de Buenos Aires. Facultad de Medicina. Centro de Estudios Farmacológicos y Botánicos; Argentina
LXVI Reunión anual de la Sociedad Argentina de Investigación Clínica; LXIX Reunión Anual de la Sociedad Argentina de Inmunología; LIII Reunión Anual de la Asociación Argentina de Farmacología Experimental y XI Reunión Anual de la Asociación Argentina de Nanomedicinas
Buenos Aires
Argentina
Sociedad Argentina de Investigación Clínica
Sociedad Argentina de Inmunología
Asociación Argentina de Farmacología Experimental
Asociación Argentina de Nanomedicinas
Materia
B1 cells
pregnancy
anti-inflamatory
proliferative profile
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/194886
Acceder
id CONICETDig_a35a229d0afd306de225ae3fe640133e
oai_identifier_str oai:ri.conicet.gov.ar:11336/194886
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling B1 B cells acquire a proliferative and anti-inflammatory profile during pregnancy in miceValeff, Natalin JimenaAbba, Martin C.Jensen, FedericoB1 cellspregnancyanti-inflamatoryproliferative profilehttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3B1 B cells are a distinct subpopulation of B cells characterized by their unique capacity of self-renewal and the ability to secrete IgM without foreign antigen exposure (natural antibodies). In addition, upon activation, B1 B cells produce large quantities of the potent anti-inflammatory cytokine IL-10. Though the mechanisms that control natural antibodies production are not fully elucidated, it was recently associated with a down-regulation of CD1d expression in B1 B cells. Taking into account that both, IL-10 and natural antibodies are known to be fundamental components in pregnancy wellbeing, the aim of this study was to evaluate proliferation status as well as CD1d expression and IL-10 production by B1 B cells during pregnancy. Flow cytometry analysis, on splenic B1 B cells from pregnant (P) and non-pregnant (NP) mice was performed to evaluate ki-67 (proliferation marker) and CD1d expression as well as IL-10 production upon LPS stimulation. We observed significantly higher expression levels of Ki-67 in splenic B1 B cells from P compared to NP (Unpaired t-test p<0,0001; n=3) mice which was mirrored by higher percentages of B1 B cells in the spleen of P mice (Unpaired t-test p=0,0095; n=11). In addition, B1 B cells from P mice expressed lower levels of CD1d as compared to NP mice (Unpaired t-test p<0,0001; n=3). Furthermore, LPS-stimulated B1 B cells from P mice produced significantly higher levels of IL-10 compared to NP mice in vitro (Unpaired t-test p=0,015; n=5).Overall, our results demonstrate that not only B1 B cells are expanded in the spleen during pregnancy but they also seem to acquire the capacity to produce higher levels of natural antibodies and IL-10 during this period, suggesting their critical role in the intricate process of pregnancy tolerance.Fil: Valeff, Natalin Jimena. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Centro de Estudios Farmacológicos y Botánicos. Universidad de Buenos Aires. Facultad de Medicina. Centro de Estudios Farmacológicos y Botánicos; ArgentinaFil: Abba, Martin C.. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Centro de Investigaciones Inmunológicas Básicas y Aplicadas; ArgentinaFil: Jensen, Federico. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Centro de Estudios Farmacológicos y Botánicos. Universidad de Buenos Aires. Facultad de Medicina. Centro de Estudios Farmacológicos y Botánicos; ArgentinaLXVI Reunión anual de la Sociedad Argentina de Investigación Clínica; LXIX Reunión Anual de la Sociedad Argentina de Inmunología; LIII Reunión Anual de la Asociación Argentina de Farmacología Experimental y XI Reunión Anual de la Asociación Argentina de NanomedicinasBuenos AiresArgentinaSociedad Argentina de Investigación ClínicaSociedad Argentina de InmunologíaAsociación Argentina de Farmacología ExperimentalAsociación Argentina de NanomedicinasFundación Revista Medicina2021info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectReuniónJournalhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/194886B1 B cells acquire a proliferative and anti-inflammatory profile during pregnancy in mice; LXVI Reunión anual de la Sociedad Argentina de Investigación Clínica; LXIX Reunión Anual de la Sociedad Argentina de Inmunología; LIII Reunión Anual de la Asociación Argentina de Farmacología Experimental y XI Reunión Anual de la Asociación Argentina de Nanomedicinas; Buenos Aires; Argentina; 2021; 121-1211669-9106CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://medicinabuenosaires.com/revistas/vol81-21/s3/Mv81s3.pdfNacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:48:15Zoai:ri.conicet.gov.ar:11336/194886instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:48:15.759CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv B1 B cells acquire a proliferative and anti-inflammatory profile during pregnancy in mice
title B1 B cells acquire a proliferative and anti-inflammatory profile during pregnancy in mice
spellingShingle B1 B cells acquire a proliferative and anti-inflammatory profile during pregnancy in mice
Valeff, Natalin Jimena
B1 cells
pregnancy
anti-inflamatory
proliferative profile
title_short B1 B cells acquire a proliferative and anti-inflammatory profile during pregnancy in mice
title_full B1 B cells acquire a proliferative and anti-inflammatory profile during pregnancy in mice
title_fullStr B1 B cells acquire a proliferative and anti-inflammatory profile during pregnancy in mice
title_full_unstemmed B1 B cells acquire a proliferative and anti-inflammatory profile during pregnancy in mice
title_sort B1 B cells acquire a proliferative and anti-inflammatory profile during pregnancy in mice
dc.creator.none.fl_str_mv Valeff, Natalin Jimena
Abba, Martin C.
Jensen, Federico
author Valeff, Natalin Jimena
author_facet Valeff, Natalin Jimena
Abba, Martin C.
Jensen, Federico
author_role author
author2 Abba, Martin C.
Jensen, Federico
author2_role author
author
dc.subject.none.fl_str_mv B1 cells
pregnancy
anti-inflamatory
proliferative profile
topic B1 cells
pregnancy
anti-inflamatory
proliferative profile
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.1
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv B1 B cells are a distinct subpopulation of B cells characterized by their unique capacity of self-renewal and the ability to secrete IgM without foreign antigen exposure (natural antibodies). In addition, upon activation, B1 B cells produce large quantities of the potent anti-inflammatory cytokine IL-10. Though the mechanisms that control natural antibodies production are not fully elucidated, it was recently associated with a down-regulation of CD1d expression in B1 B cells. Taking into account that both, IL-10 and natural antibodies are known to be fundamental components in pregnancy wellbeing, the aim of this study was to evaluate proliferation status as well as CD1d expression and IL-10 production by B1 B cells during pregnancy. Flow cytometry analysis, on splenic B1 B cells from pregnant (P) and non-pregnant (NP) mice was performed to evaluate ki-67 (proliferation marker) and CD1d expression as well as IL-10 production upon LPS stimulation. We observed significantly higher expression levels of Ki-67 in splenic B1 B cells from P compared to NP (Unpaired t-test p<0,0001; n=3) mice which was mirrored by higher percentages of B1 B cells in the spleen of P mice (Unpaired t-test p=0,0095; n=11). In addition, B1 B cells from P mice expressed lower levels of CD1d as compared to NP mice (Unpaired t-test p<0,0001; n=3). Furthermore, LPS-stimulated B1 B cells from P mice produced significantly higher levels of IL-10 compared to NP mice in vitro (Unpaired t-test p=0,015; n=5).Overall, our results demonstrate that not only B1 B cells are expanded in the spleen during pregnancy but they also seem to acquire the capacity to produce higher levels of natural antibodies and IL-10 during this period, suggesting their critical role in the intricate process of pregnancy tolerance.
Fil: Valeff, Natalin Jimena. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Centro de Estudios Farmacológicos y Botánicos. Universidad de Buenos Aires. Facultad de Medicina. Centro de Estudios Farmacológicos y Botánicos; Argentina
Fil: Abba, Martin C.. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Centro de Investigaciones Inmunológicas Básicas y Aplicadas; Argentina
Fil: Jensen, Federico. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Centro de Estudios Farmacológicos y Botánicos. Universidad de Buenos Aires. Facultad de Medicina. Centro de Estudios Farmacológicos y Botánicos; Argentina
LXVI Reunión anual de la Sociedad Argentina de Investigación Clínica; LXIX Reunión Anual de la Sociedad Argentina de Inmunología; LIII Reunión Anual de la Asociación Argentina de Farmacología Experimental y XI Reunión Anual de la Asociación Argentina de Nanomedicinas
Buenos Aires
Argentina
Sociedad Argentina de Investigación Clínica
Sociedad Argentina de Inmunología
Asociación Argentina de Farmacología Experimental
Asociación Argentina de Nanomedicinas
description B1 B cells are a distinct subpopulation of B cells characterized by their unique capacity of self-renewal and the ability to secrete IgM without foreign antigen exposure (natural antibodies). In addition, upon activation, B1 B cells produce large quantities of the potent anti-inflammatory cytokine IL-10. Though the mechanisms that control natural antibodies production are not fully elucidated, it was recently associated with a down-regulation of CD1d expression in B1 B cells. Taking into account that both, IL-10 and natural antibodies are known to be fundamental components in pregnancy wellbeing, the aim of this study was to evaluate proliferation status as well as CD1d expression and IL-10 production by B1 B cells during pregnancy. Flow cytometry analysis, on splenic B1 B cells from pregnant (P) and non-pregnant (NP) mice was performed to evaluate ki-67 (proliferation marker) and CD1d expression as well as IL-10 production upon LPS stimulation. We observed significantly higher expression levels of Ki-67 in splenic B1 B cells from P compared to NP (Unpaired t-test p<0,0001; n=3) mice which was mirrored by higher percentages of B1 B cells in the spleen of P mice (Unpaired t-test p=0,0095; n=11). In addition, B1 B cells from P mice expressed lower levels of CD1d as compared to NP mice (Unpaired t-test p<0,0001; n=3). Furthermore, LPS-stimulated B1 B cells from P mice produced significantly higher levels of IL-10 compared to NP mice in vitro (Unpaired t-test p=0,015; n=5).Overall, our results demonstrate that not only B1 B cells are expanded in the spleen during pregnancy but they also seem to acquire the capacity to produce higher levels of natural antibodies and IL-10 during this period, suggesting their critical role in the intricate process of pregnancy tolerance.
publishDate 2021
dc.date.none.fl_str_mv 2021
dc.type.none.fl_str_mv info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/conferenceObject
Reunión
Journal
http://purl.org/coar/resource_type/c_5794
info:ar-repo/semantics/documentoDeConferencia
status_str publishedVersion
format conferenceObject
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/194886
B1 B cells acquire a proliferative and anti-inflammatory profile during pregnancy in mice; LXVI Reunión anual de la Sociedad Argentina de Investigación Clínica; LXIX Reunión Anual de la Sociedad Argentina de Inmunología; LIII Reunión Anual de la Asociación Argentina de Farmacología Experimental y XI Reunión Anual de la Asociación Argentina de Nanomedicinas; Buenos Aires; Argentina; 2021; 121-121
1669-9106
CONICET Digital
CONICET
url http://hdl.handle.net/11336/194886
identifier_str_mv B1 B cells acquire a proliferative and anti-inflammatory profile during pregnancy in mice; LXVI Reunión anual de la Sociedad Argentina de Investigación Clínica; LXIX Reunión Anual de la Sociedad Argentina de Inmunología; LIII Reunión Anual de la Asociación Argentina de Farmacología Experimental y XI Reunión Anual de la Asociación Argentina de Nanomedicinas; Buenos Aires; Argentina; 2021; 121-121
1669-9106
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://medicinabuenosaires.com/revistas/vol81-21/s3/Mv81s3.pdf
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
dc.coverage.none.fl_str_mv Nacional
dc.publisher.none.fl_str_mv Fundación Revista Medicina
publisher.none.fl_str_mv Fundación Revista Medicina
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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