Intrabone marrow diversity of endothelial cells and its impact on hematopoietic stem cell development and maintenance.

IF 2.5 4区 医学 Q2 HEMATOLOGY
Shota Shimizu, Yoshiaki Kubota
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引用次数: 0

Abstract

In addition to supplying oxygen and nutrients, blood vessels secrete paracrine molecules known as angiocrine factors to promote tissue homeostasis and repair. The bone marrow (BM) vasculature in long bones has differing properties between the diaphysis, metaphysis, and epiphysis in terms of its morphology, plasticity, perivascular cellular components, and angiocrine profiles. Blood vessel formation is linked with bone formation through paracrine interactions between endothelial cells (ECs) and osteolineage cells, so-called angiogenic-osteogenic coupling. ECs also play essential roles in the maintenance of hematopoietic stem cells (HSCs) by forming vascular niches together with perivascular stromal cells. Recent studies highlighted the heterogeneity of vascular niches at different bone regions, suggesting that HSCs are regulated by locally distinct mechanisms. Here, we provided an overview of the BM vasculature and discussed how the heterogeneous vasculature contributes to bone formation and HSC maintenance.

骨髓内内皮细胞多样性及其对造血干细胞发育和维持的影响。
除了提供氧气和营养外,血管还分泌被称为血管分泌因子的旁分泌分子来促进组织稳态和修复。长骨中的骨髓(BM)血管系统在骨干、干骺和骨骺的形态、可塑性、血管周围细胞成分和血管分泌谱方面具有不同的特性。血管的形成与骨的形成是通过内皮细胞(ECs)和骨系细胞之间的旁分泌相互作用,即所谓的血管生成-成骨耦合而联系在一起的。内皮细胞还通过与血管周围基质细胞一起形成血管壁龛,在造血干细胞(hsc)的维持中发挥重要作用。最近的研究强调了不同骨区域血管壁龛的异质性,表明造血干细胞受局部不同机制的调节。在这里,我们提供了BM血管系统的概述,并讨论了异质血管系统如何促进骨形成和HSC维持。摘要:长骨的骨髓(BM)血管系统在不同的骨区具有不同的特性。血管的形成与骨的形成密切相关,这一过程被称为血管生成-成骨耦合。骨髓血管系统也通过建立血管壁龛来支持造血干细胞(hsc)。最近的研究强调了不同骨区域血管壁龛的区域异质性,表明造血干细胞受局部不同机制的调节。这篇综述概述了BM血管系统,并研究了其异质性如何影响骨形成和HSC维持。
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来源期刊
Experimental hematology
Experimental hematology 医学-血液学
CiteScore
5.30
自引率
0.00%
发文量
84
审稿时长
58 days
期刊介绍: Experimental Hematology publishes new findings, methodologies, reviews and perspectives in all areas of hematology and immune cell formation on a monthly basis that may include Special Issues on particular topics of current interest. The overall goal is to report new insights into how normal blood cells are produced, how their production is normally regulated, mechanisms that contribute to hematological diseases and new approaches to their treatment. Specific topics may include relevant developmental and aging processes, stem cell biology, analyses of intrinsic and extrinsic regulatory mechanisms, in vitro behavior of primary cells, clonal tracking, molecular and omics analyses, metabolism, epigenetics, bioengineering approaches, studies in model organisms, novel clinical observations, transplantation biology and new therapeutic avenues.
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