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Plasma cell differentiation is regulated by the expression of histone variant H3.3.
Saito, Yuichi; Harada, Akihito; Ushijima, Miho; Tanaka, Kaori; Higuchi, Ryota; Baba, Akemi; Murakami, Daisuke; Nutt, Stephen L; Nakagawa, Takashi; Ohkawa, Yasuyuki; Baba, Yoshihiro.
Afiliação
  • Saito Y; Division of Immunology and Genome Biology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
  • Harada A; Department of Otorhinolaryngology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Ushijima M; Division of Transcriptomics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
  • Tanaka K; Division of Immunology and Genome Biology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
  • Higuchi R; Division of Transcriptomics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
  • Baba A; Division of Immunology and Genome Biology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
  • Murakami D; Department of Otorhinolaryngology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Nutt SL; Division of Immunology and Genome Biology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
  • Nakagawa T; Department of Otorhinolaryngology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Ohkawa Y; The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, 3050, Australia.
  • Baba Y; Department of Medical Biology, The University of Melbourne, Parkville, VIC, 3010, Australia.
Nat Commun ; 15(1): 5004, 2024 Jun 20.
Article em En | MEDLINE | ID: mdl-38902223
ABSTRACT
The differentiation of B cells into plasma cells is associated with substantial transcriptional and epigenetic remodeling. H3.3 histone variant marks active chromatin via replication-independent nucleosome assembly. However, its role in plasma cell development remains elusive. Herein, we show that during plasma cell differentiation, H3.3 is downregulated, and the deposition of H3.3 and chromatin accessibility are dynamically changed. Blockade of H3.3 downregulation by enforced H3.3 expression impairs plasma cell differentiation in an H3.3-specific sequence-dependent manner. Mechanistically, enforced H3.3 expression inhibits the upregulation of plasma cell-associated genes such as Irf4, Prdm1, and Xbp1 and maintains the expression of B cell-associated genes, Pax5, Bach2, and Bcl6. Concomitantly, sustained H3.3 expression prevents the structure of chromatin accessibility characteristic for plasma cells. Our findings suggest that appropriate H3.3 expression and deposition control plasma cell differentiation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasmócitos / Histonas / Diferenciação Celular Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasmócitos / Histonas / Diferenciação Celular Idioma: En Ano de publicação: 2024 Tipo de documento: Article