4.7 Review

Microbial Sensing by Hematopoietic Stem and Progenitor Cells

期刊

STEM CELLS
卷 40, 期 1, 页码 14-21

出版社

OXFORD UNIV PRESS
DOI: 10.1093/stmcls/sxab007

关键词

hematopoietic stem and progenitor cells; bone marrow; emergency myelopoiesis; infection; microbiome; pathogens

资金

  1. National Institutes of Health [R01 AI134987]
  2. Board of Governors Regenerative Medicine Institute at Cedars-Sinai Medical Center

向作者/读者索取更多资源

Balanced production of immune cells is important for immune surveillance, and commensal microbes can influence hematopoietic stem and progenitor cell (HSPC) activity. HSPCs sense microbes through pattern recognition receptors and cytokine receptors, and the long-term effects of microbial stimuli on HSPCs are significant. There may be a connection between myeloid-biased hematopoiesis and elevated levels of microbiome-derived components in aging and metabolic stress. Trained immunity-based vaccines that exploit microbial stimulation of HSPCs show promise.
Balanced production of immune cells is critical for the maintenance of steady-state immune surveillance, and increased production of myeloid cells is sometimes necessary to eliminate pathogens. Hematopoietic stem and progenitor cell (HSPC) sensing of commensal microbes and invading pathogens has a notable impact on hematopoiesis. In this review, we examine how commensal microbes regulate bone marrow HSPC activity to maintain balanced hematopoiesis in the steady state, and how HSPCs proliferate and differentiate during emergency myelopoiesis in response to infection. HSPCs express a variety of pattern recognition receptors and cytokine receptors that they use to sense the presence of microbes, either directly via detection of microbial components and metabolites, or indirectly by responding to cytokines produced by other host cells. We describe direct and indirect mechanisms of microbial sensing by HSPCs and highlight evidence demonstrating long-term effects of acute and chronic microbial stimuli on HSPCs. We also discuss a possible connection between myeloid-biased hematopoiesis and elevated levels of circulating microbiome-derived components in the context of aging and metabolic stress. Finally, we highlight the prospect of trained immunity-based vaccines that could exploit microbial stimulation of HSPCs.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据