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Hematopoietic stem cell-independent hematopoiesis and the origins of innate-like B lymphocytes.
Ghosn, Eliver; Yoshimoto, Momoko; Nakauchi, Hiromitsu; Weissman, Irving L; Herzenberg, Leonore A.
Afiliação
  • Ghosn E; Departments of Medicine and Pediatrics, Lowance Center for Human Immunology, Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322, USA eliver.ghosn@emory.edu.
  • Yoshimoto M; Center for Stem Cell and Regenerative Medicine, Institute of Molecular Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
  • Nakauchi H; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Weissman IL; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Herzenberg LA; Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.
Development ; 146(15)2019 08 01.
Article em En | MEDLINE | ID: mdl-31371526
ABSTRACT
The current paradigm that a single long-term hematopoietic stem cell can regenerate all components of the mammalian immune system has been challenged by recent findings in mice. These findings show that adult tissue-resident macrophages and innate-like lymphocytes develop early in fetal hematopoiesis from progenitors that emerge prior to, and apparently independently of, conventional long-term hematopoietic stem cells. Here, we discuss these recent findings, which show that an early and distinct wave of hematopoiesis occurs for all major hematopoietic lineages. These data provide evidence that fetal hematopoietic progenitors not derived from the bona fide long-term hematopoietic stem cells give rise to tissue-resident immune cells that persist throughout adulthood. We also discuss recent insights into B lymphocyte development and attempt to synthesize seemingly contradictory recent findings on the origins of innate-like B-1a lymphocytes during fetal hematopoiesis.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco Hematopoéticas / Subpopulações de Linfócitos B / Hematopoese / Macrófagos Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco Hematopoéticas / Subpopulações de Linfócitos B / Hematopoese / Macrófagos Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article