| Literature DB >> 27590115 |
Catherine M Sawai1, Sonja Babovic2, Samik Upadhaya3, David J H F Knapp2, Yonit Lavin4, Colleen M Lau5, Anton Goloborodko6, Jue Feng5, Joji Fujisaki7, Lei Ding8, Leonid A Mirny9, Miriam Merad4, Connie J Eaves2, Boris Reizis10.
Abstract
Hematopoietic stem cells (HSCs) sustain long-term reconstitution of hematopoiesis in transplantation recipients, yet their role in the endogenous steady-state hematopoiesis remains unclear. In particular, recent studies suggested that HSCs provide a relatively minor contribution to immune cell development in adults. We directed transgene expression in a fraction of HSCs that maintained reconstituting activity during serial transplantations. Inducible genetic labeling showed that transgene-expressing HSCs gave rise to other phenotypic HSCs, confirming their top position in the differentiation hierarchy. The labeled HSCs rapidly contributed to committed progenitors of all lineages and to mature myeloid cells and lymphocytes, but not to B-1a cells or tissue macrophages. Importantly, labeled HSCs gave rise to more than two-thirds of all myeloid cells and platelets in adult mice, and this contribution could be accelerated by an induced interferon response. Thus, classically defined HSCs maintain immune cell development in the steady state and during systemic cytokine responses.Entities:
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Year: 2016 PMID: 27590115 PMCID: PMC5054720 DOI: 10.1016/j.immuni.2016.08.007
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745