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CD36 and LC3B initiated autophagy in B cells regulates the humoral immune response

Scavenger receptors are pattern recognition receptors that recognize both foreign and self-ligands, and initiate different mechanisms of cellular activation, often as co-receptors. The function of scavenger receptor CD36 in the immune system has mostly been studied in macrophages but it is also high...

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Autores principales: He, Chenfei, Wang, Shan, Zhou, Chikai, He, Minghui, Wang, Jin, Ladds, Marcus, Lianoudaki, Danai, Sedimbi, Saikiran K., Lane, David P., Westerberg, Lisa S., Li, Shuijie, Karlsson, Mikael C.I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8632284/
https://www.ncbi.nlm.nih.gov/pubmed/33535890
http://dx.doi.org/10.1080/15548627.2021.1885183
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author He, Chenfei
Wang, Shan
Zhou, Chikai
He, Minghui
Wang, Jin
Ladds, Marcus
Lianoudaki, Danai
Sedimbi, Saikiran K.
Lane, David P.
Westerberg, Lisa S.
Li, Shuijie
Karlsson, Mikael C.I.
author_facet He, Chenfei
Wang, Shan
Zhou, Chikai
He, Minghui
Wang, Jin
Ladds, Marcus
Lianoudaki, Danai
Sedimbi, Saikiran K.
Lane, David P.
Westerberg, Lisa S.
Li, Shuijie
Karlsson, Mikael C.I.
author_sort He, Chenfei
collection PubMed
description Scavenger receptors are pattern recognition receptors that recognize both foreign and self-ligands, and initiate different mechanisms of cellular activation, often as co-receptors. The function of scavenger receptor CD36 in the immune system has mostly been studied in macrophages but it is also highly expressed by innate type B cells where its function is less explored. Here we report that CD36 is involved in macro-autophagy/autophagy in B cells, and in its absence, the humoral immune response is impaired. We found that CD36-deficient B cells exhibit a significantly reduced plasma cell formation, proliferation, mitochondrial mobilization and oxidative phosphorylation. These changes were accompanied by impaired initiation of autophagy, and we found that CD36 regulated autophagy and colocalized with autophagosome membrane protein MAP1LC3/LC3 (microtubule-associated protein 1 light chain 3). When we investigated T-cell-dependent immune responses, we found that mice with CD36 deficiency, specifically in B cells, exhibited attenuated germinal center responses, class switching, and antibody production as well as autophagosome formation. These findings establish a critical role for CD36 in B cell responses and may also contribute to our understanding of CD36-mediated autophagy in other cells as well as in B cell lymphomas that have been shown to express the receptor. Abbreviations: AICDA/AID: activation-induced cytidine deaminase; ATG5: autophagy related 5; ATP: adenosine triphosphate; BCR: B-cell receptor; CPG: unmethylated cytosine-guanosine; CQ: chloroquine; DC: dendritic cells; FOB: follicular B cells; GC: germinal center; Ig: immunoglobulin; LPS: lipopolysaccharide; MAP1LC3/LC3: microtubule-associated protein 1 light chain 3; MFI: mean fluorescence intensity; MZB: marginal zone B cells; NP-CGG: 4-hydroxy-3-nitrophenylacetyl-chicken gamma globulin; OCR: oxygen consumption rate; oxLDL: oxidized low-density lipoprotein; PC: plasma cells; Rapa: rapamycin; SQSTM1/p62: sequestosome 1; SRBC: sheep red blood cells; Tfh: follicular helper T cells; TLR: toll-like receptor.
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spelling pubmed-86322842021-12-01 CD36 and LC3B initiated autophagy in B cells regulates the humoral immune response He, Chenfei Wang, Shan Zhou, Chikai He, Minghui Wang, Jin Ladds, Marcus Lianoudaki, Danai Sedimbi, Saikiran K. Lane, David P. Westerberg, Lisa S. Li, Shuijie Karlsson, Mikael C.I. Autophagy Research Paper Scavenger receptors are pattern recognition receptors that recognize both foreign and self-ligands, and initiate different mechanisms of cellular activation, often as co-receptors. The function of scavenger receptor CD36 in the immune system has mostly been studied in macrophages but it is also highly expressed by innate type B cells where its function is less explored. Here we report that CD36 is involved in macro-autophagy/autophagy in B cells, and in its absence, the humoral immune response is impaired. We found that CD36-deficient B cells exhibit a significantly reduced plasma cell formation, proliferation, mitochondrial mobilization and oxidative phosphorylation. These changes were accompanied by impaired initiation of autophagy, and we found that CD36 regulated autophagy and colocalized with autophagosome membrane protein MAP1LC3/LC3 (microtubule-associated protein 1 light chain 3). When we investigated T-cell-dependent immune responses, we found that mice with CD36 deficiency, specifically in B cells, exhibited attenuated germinal center responses, class switching, and antibody production as well as autophagosome formation. These findings establish a critical role for CD36 in B cell responses and may also contribute to our understanding of CD36-mediated autophagy in other cells as well as in B cell lymphomas that have been shown to express the receptor. Abbreviations: AICDA/AID: activation-induced cytidine deaminase; ATG5: autophagy related 5; ATP: adenosine triphosphate; BCR: B-cell receptor; CPG: unmethylated cytosine-guanosine; CQ: chloroquine; DC: dendritic cells; FOB: follicular B cells; GC: germinal center; Ig: immunoglobulin; LPS: lipopolysaccharide; MAP1LC3/LC3: microtubule-associated protein 1 light chain 3; MFI: mean fluorescence intensity; MZB: marginal zone B cells; NP-CGG: 4-hydroxy-3-nitrophenylacetyl-chicken gamma globulin; OCR: oxygen consumption rate; oxLDL: oxidized low-density lipoprotein; PC: plasma cells; Rapa: rapamycin; SQSTM1/p62: sequestosome 1; SRBC: sheep red blood cells; Tfh: follicular helper T cells; TLR: toll-like receptor. Taylor & Francis 2021-02-16 /pmc/articles/PMC8632284/ /pubmed/33535890 http://dx.doi.org/10.1080/15548627.2021.1885183 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper
He, Chenfei
Wang, Shan
Zhou, Chikai
He, Minghui
Wang, Jin
Ladds, Marcus
Lianoudaki, Danai
Sedimbi, Saikiran K.
Lane, David P.
Westerberg, Lisa S.
Li, Shuijie
Karlsson, Mikael C.I.
CD36 and LC3B initiated autophagy in B cells regulates the humoral immune response
title CD36 and LC3B initiated autophagy in B cells regulates the humoral immune response
title_full CD36 and LC3B initiated autophagy in B cells regulates the humoral immune response
title_fullStr CD36 and LC3B initiated autophagy in B cells regulates the humoral immune response
title_full_unstemmed CD36 and LC3B initiated autophagy in B cells regulates the humoral immune response
title_short CD36 and LC3B initiated autophagy in B cells regulates the humoral immune response
title_sort cd36 and lc3b initiated autophagy in b cells regulates the humoral immune response
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8632284/
https://www.ncbi.nlm.nih.gov/pubmed/33535890
http://dx.doi.org/10.1080/15548627.2021.1885183
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