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造血干细胞及其后代的龛位。

Niches for Hematopoietic Stem Cells and Their Progeny.

机构信息

Ruth L. and David S. Gottesman Institute for Stem Cell and Regenerative Medicine Research, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

Ruth L. and David S. Gottesman Institute for Stem Cell and Regenerative Medicine Research, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Departmentof Medicine, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Immunity. 2018 Apr 17;48(4):632-648. doi: 10.1016/j.immuni.2018.03.024.

DOI:10.1016/j.immuni.2018.03.024
PMID:29669248
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6103525/
Abstract

Steady-state hematopoietic stem cells' (HSCs) self-renewal and differentiation toward their mature progeny in the adult bone marrow is tightly regulated by cues from the microenvironment. Recent insights into the cellular and molecular constituents have uncovered a high level of complexity. Here, we review emerging evidence showing how HSCs and their progeny are regulated by an interdependent network of mesenchymal stromal cells, nerve fibers, the vasculature, and also other hematopoietic cells. Understanding the interaction mechanisms in these intricate niches will provide great opportunities for HSC-related therapies and immune modulation.

摘要

稳态造血干细胞(HSCs)在成人骨髓中的自我更新和向其成熟后代的分化受到来自微环境的信号的严格调控。最近对细胞和分子成分的深入了解揭示了高度的复杂性。在这里,我们回顾了新出现的证据,展示了 HSCs 及其后代如何受到间充质基质细胞、神经纤维、血管以及其他造血细胞的相互依存的网络的调节。了解这些复杂生态位中的相互作用机制将为与 HSC 相关的治疗和免疫调节提供巨大机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cabe/6103525/71b6419a3709/nihms958579f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cabe/6103525/eb17f918392f/nihms958579f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cabe/6103525/71b6419a3709/nihms958579f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cabe/6103525/eb17f918392f/nihms958579f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cabe/6103525/71b6419a3709/nihms958579f2.jpg

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本文引用的文献

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CD150 Bone Marrow Tregs Maintain Hematopoietic Stem Cell Quiescence and Immune Privilege via Adenosine.CD150+ 骨髓 Tregs 通过腺苷维持造血干细胞静止和免疫豁免。
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Lineage-Biased Hematopoietic Stem Cells Are Regulated by Distinct Niches.基于谱系的造血干细胞受不同龛位的调控。
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Clonal analysis of lineage fate in native haematopoiesis.
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