4.5 Review

Identification of microenvironmental niches for hematopoietic stem cells and lymphoid progenitors-bone marrow fibroblastic reticular cells with salient features

期刊

INTERNATIONAL IMMUNOLOGY
卷 33, 期 12, 页码 821-826

出版社

OXFORD UNIV PRESS
DOI: 10.1093/intimm/dxab092

关键词

B cells; HSCs; lymphopoiesis; mesenchymal stem cells; microenvironments

资金

  1. Japan Society for the Promotion of Science [18H03998]
  2. Grants-in-Aid for Scientific Research [18H03998] Funding Source: KAKEN

向作者/读者索取更多资源

Most blood cells, including immune cells, are generated from hematopoietic stem cells in bone marrow, which require specialized microenvironments called niches; recent studies have identified CAR cells as the major component of niches for HSCs and lymphoid progenitors, expressing high levels of critical niche factors and functioning as self-renewing mesenchymal stem cells. The findings provide insights into the interaction between hematopoietic cells and microenvironments in health and disease.
Most lineages of blood cells, including immune cells, are generated from hematopoietic stem cells (HSCs) in bone marrow throughout adult life. Since HSCs cannot expand on their own, they require and contact the special microenvironments, termed niches for their maintenance. HSC niches comprise supportive cells that provide adjacent HSCs with critical signals, including cytokines. Although bone marrow microenvironments have been thought to be complex, recent studies have demonstrated that the bone marrow-specific population of fibroblastic reticular cells with long processes, termed CXC chemokine ligand 12 (CXCL12)-abundant reticular (CAR) cells, which overlap strongly with leptin receptor (LepR)-expressing (LepR(+)) cells, is the major cellular component of niches for HSCs and lymphoid progenitors. CAR cells have salient features, expressing much higher levels of critical HSC niche factors than any other cell populations and function as self-renewing mesenchymal stem cells. Human counterpart of CAR cells is present and affected in diseases, including leukemia. Foxl1(+) telocytes recently identified as the niche for intestinal stem cells share some features with CAR cells, suggesting that CAR cells might serve as a prototype for fibroblastic reticular cells creating niche for long-lived cells, including tissue stem cells and memory lymphocytes. These findings provided the basis for future mechanistic studies on the cross-talk between hematopoietic cells and microenvironments in both health and disease.

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

4.5
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