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造血干细胞稳态、再生及衰老的血管调节

Vascular Regulation of Hematopoietic Stem Cell Homeostasis, Regeneration, and Aging.

作者信息

Ramalingam Pradeep, Butler Jason M, Poulos Michael G

机构信息

Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, NJ USA.

Molecular and Experimental Therapeutic Research in Oncology Program, Georgetown University, Washington, DC USA.

出版信息

Curr Stem Cell Rep. 2021;7(4):194-203. doi: 10.1007/s40778-021-00198-2. Epub 2021 Sep 4.

Abstract

PURPOSE OF REVIEW

Hematopoietic stem cells (HSCs) sit at the top of the hierarchy that meets the daily burden of blood production. HSC maintenance relies on extrinsic cues from the bone marrow (BM) microenvironment to balance stem cell self-renewal and cell fate decisions. In this brief review, we will highlight the studies and model systems that define the centralized role of BM vascular endothelium in modulating HSC activity in health and stress.

RECENT FINDINGS

The BM microenvironment is composed of a diverse array of intimately associated vascular and perivascular cell types. Recent dynamic imaging studies, coupled with single-cell RNA sequencing (scRNA-seq) and functional readouts, have advanced our understanding of the HSC-supportive cell types and their cooperative mechanisms that govern stem cell fate during homeostasis, regeneration, and aging. These findings have established complex and discrete vascular microenvironments within the BM that express overlapping and unique paracrine signals that modulate HSC fate.

SUMMARY

Understanding the spatial and reciprocal HSC-niche interactions and the molecular mechanisms that govern HSC activity in the BM vascular microenvironment will be integral in developing therapies aimed at ameliorating hematological disease and supporting healthy hematopoietic output.

摘要

综述目的

造血干细胞(HSCs)处于满足日常血液生成需求的细胞层级顶端。造血干细胞的维持依赖于来自骨髓(BM)微环境的外在信号,以平衡干细胞自我更新和细胞命运决定。在这篇简短的综述中,我们将重点介绍那些明确骨髓血管内皮在健康和应激状态下调节造血干细胞活性中核心作用的研究及模型系统。

最新发现

骨髓微环境由多种紧密相关的血管和血管周围细胞类型组成。最近的动态成像研究,结合单细胞RNA测序(scRNA-seq)和功能读数分析,加深了我们对造血干细胞支持性细胞类型及其在稳态、再生和衰老过程中调控干细胞命运的协同机制的理解。这些发现揭示了骨髓内复杂且不同的血管微环境,它们表达重叠且独特的旁分泌信号来调节造血干细胞命运。

总结

了解骨髓血管微环境中造血干细胞与龛位之间的空间及相互作用,以及调控造血干细胞活性的分子机制,对于开发旨在改善血液疾病和支持健康造血输出的治疗方法至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5990/8639543/bc923f80c163/40778_2021_198_Fig1_HTML.jpg

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