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Postmitotic G1 phase survivin drives mitogen-independent cell division of B lymphocytes.
Singh, Amit; Spitzer, Matthew H; Joy, Jaimy P; Kaileh, Mary; Qiu, Xiang; Nolan, Garry P; Sen, Ranjan.
Afiliação
  • Singh A; Gene Regulation Section, Laboratory of Molecular Biology and Immunology, National Institute on Aging, Baltimore, MD 21224.
  • Spitzer MH; Department of Microbiology and Immunology, Baxter Laboratory of Stem Cell Biology, Stanford University, School of Medicine, Stanford, CA 94305.
  • Joy JP; Gene Regulation Section, Laboratory of Molecular Biology and Immunology, National Institute on Aging, Baltimore, MD 21224.
  • Kaileh M; Gene Regulation Section, Laboratory of Molecular Biology and Immunology, National Institute on Aging, Baltimore, MD 21224.
  • Qiu X; Gene Regulation Section, Laboratory of Molecular Biology and Immunology, National Institute on Aging, Baltimore, MD 21224.
  • Nolan GP; Department of Microbiology and Immunology, Baxter Laboratory of Stem Cell Biology, Stanford University, School of Medicine, Stanford, CA 94305.
  • Sen R; Gene Regulation Section, Laboratory of Molecular Biology and Immunology, National Institute on Aging, Baltimore, MD 21224.
Proc Natl Acad Sci U S A ; 119(18): e2115567119, 2022 05 03.
Article em En | MEDLINE | ID: mdl-35476510
ABSTRACT
B and T lymphocytes of the adaptive immune system undergo proliferative bursts to generate pools of antigen-specific cells for effective immunity. Here we show that in contrast to the canonical view that G1 progression signals are essential after mitosis to reenter S phase, B lymphocytes sustain several rounds of mitogen-independent cell division following the first mitosis. Such division appears to be driven by unique characteristics of the postmitotic G1 phase that has features of S and G2/M phases. Birc5 (survivin), a protein associated with chromosome segregation in G2/M, is expressed in the G1 phase of divided B cells and is necessary for mitogen-independent divisions. The partially active G1 phase and propensity for apoptosis inherited after each division may underlie rapid proliferation and cell death, which are hallmarks of B cell proliferative responses.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteômica / Mitógenos Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteômica / Mitógenos Idioma: En Ano de publicação: 2022 Tipo de documento: Article