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Bach2 repression of CD36 regulates lipid-metabolism-linked effector functions in follicular B cells

The transcription repressor Bach2 plays a crucial role in shaping humoral immunity, but its cell-autonomous function remains elusive. Here, we reveal the mechanism by which Bach2 regulates effector cell maturation in peripheral B cells. In response to Toll-like receptor (TLR) agonists, Bach2 deficie...

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Published in:Cell reports (Cambridge) 2024-11, Vol.43 (11), p.114878, Article 114878
Main Authors: Jang, Eunkyeong, Kim, ChangYeon, Noh, Jeonghyun, Yi, Hansol, Jo, Sungsin, Park, Jin-Sil, Hwang, Woochang, Cha, Ji-Young, Cho, Mi-La, Kim, Tae-Hwan, Youn, Jeehee
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container_issue 11
container_start_page 114878
container_title Cell reports (Cambridge)
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creator Jang, Eunkyeong
Kim, ChangYeon
Noh, Jeonghyun
Yi, Hansol
Jo, Sungsin
Park, Jin-Sil
Hwang, Woochang
Cha, Ji-Young
Cho, Mi-La
Kim, Tae-Hwan
Youn, Jeehee
description The transcription repressor Bach2 plays a crucial role in shaping humoral immunity, but its cell-autonomous function remains elusive. Here, we reveal the mechanism by which Bach2 regulates effector cell maturation in peripheral B cells. In response to Toll-like receptor (TLR) agonists, Bach2 deficiency promotes the differentiation of follicular, but not marginal zone, B cells into effector cells, producing interleukin (IL)-6 and antibodies. This phenomenon is associated with changes in lipid metabolism, such as increases in CD36 expression, lipid influx, and fatty acid oxidation. Consistent with this, Bach2-deficient B cells exhibit elevated levels of mitochondrial oxidative stress, lipid peroxidation, and p38 activation. Mechanistically, Bach2 acts as a repressor of Cd36, and inhibition of CD36 or fatty acid oxidation reduces the differentiation of naive B cells into IL-6- and antibody-secreting cells. These results indicate Bach2 as a key metabolic checkpoint regulator crucial for maintaining a functionally quiescent state of follicular B cells. [Display omitted] •Bach2 deficiency drives follicular B cells to give rise to IL-6- and Ab-producing cells•Bach2 regulates B cell lipid metabolism by acting as a transcriptional repressor of CD36•Changes in CD36-mediated lipid metabolism affect follicular B cell maturation•Bach2 is a key metabolic factor crucial for regulating follicular B cell fates Jang et al. report that Bach2 regulates the differentiation of follicular B cells into effector cells by altering CD36-mediated lipid metabolism. They identify Bach2 as a metabolic regulator crucial for determining B cell fates. This study defines a fundamental connection between the metabolic program and functions in B cells.
doi_str_mv 10.1016/j.celrep.2024.114878
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Here, we reveal the mechanism by which Bach2 regulates effector cell maturation in peripheral B cells. In response to Toll-like receptor (TLR) agonists, Bach2 deficiency promotes the differentiation of follicular, but not marginal zone, B cells into effector cells, producing interleukin (IL)-6 and antibodies. This phenomenon is associated with changes in lipid metabolism, such as increases in CD36 expression, lipid influx, and fatty acid oxidation. Consistent with this, Bach2-deficient B cells exhibit elevated levels of mitochondrial oxidative stress, lipid peroxidation, and p38 activation. Mechanistically, Bach2 acts as a repressor of Cd36, and inhibition of CD36 or fatty acid oxidation reduces the differentiation of naive B cells into IL-6- and antibody-secreting cells. These results indicate Bach2 as a key metabolic checkpoint regulator crucial for maintaining a functionally quiescent state of follicular B cells. [Display omitted] •Bach2 deficiency drives follicular B cells to give rise to IL-6- and Ab-producing cells•Bach2 regulates B cell lipid metabolism by acting as a transcriptional repressor of CD36•Changes in CD36-mediated lipid metabolism affect follicular B cell maturation•Bach2 is a key metabolic factor crucial for regulating follicular B cell fates Jang et al. report that Bach2 regulates the differentiation of follicular B cells into effector cells by altering CD36-mediated lipid metabolism. They identify Bach2 as a metabolic regulator crucial for determining B cell fates. 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subjects Animals
B cells
B-Lymphocytes - immunology
B-Lymphocytes - metabolism
Bach2
Basic-Leucine Zipper Transcription Factors - metabolism
CD36
CD36 Antigens - metabolism
Cell Differentiation
CP: Immunology
CP: Metabolism
Fatty Acids - metabolism
follicular B cells
IL-6
Interleukin-6 - metabolism
Lipid Metabolism
Mice
Mice, Inbred C57BL
Mice, Knockout
Oxidative Stress
title Bach2 repression of CD36 regulates lipid-metabolism-linked effector functions in follicular B cells
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