The osteoblastic niche in hematopoiesis and hematological myeloid malignancies.

Current molecular biology reports Pub Date : 2017-06-01 Epub Date: 2017-05-02 DOI:10.1007/s40610-017-0055-9
Marta Galán-Díez, Stavroula Kousteni
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引用次数: 31

Abstract

Purpose of review: This review focuses on evidence highlighting the bidirectional crosstalk between the hematopoietic stem cell (HSC) and their surrounding stromal cells, with a particular emphasis on cells of the osteoblast lineage. The role and molecular functions of osteoblasts in normal hematopoiesis and in myeloid hematological malignancies is discussed.

Recent findings: Cells of the osteoblast lineage have emerged as potent regulators of HSC expansion that regulate their recruitment and, depending on their stage of differentiation, their activity, proliferation and differentiation along the lymphoid, myeloid and erythroid lineages. In addition, mutations in mature osteoblasts or their progenitors induce myeloid malignancies. Conversely, signals from myelodysplastic cells can remodel the osteoblastic niche to favor self-perpetuation.

Summary: Understanding cellular crosstalk between osteoblastic cells and HSCs in the bone marrow microenvironment is of fundamental importance for developing therapies against benign and malignant hematological diseases.

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造血和血液髓系恶性肿瘤中的成骨细胞生态位。
综述目的:本综述主要关注造血干细胞(HSC)及其周围基质细胞之间双向串扰的证据,特别强调成骨细胞谱系的细胞。本文讨论了成骨细胞在正常造血和髓系恶性血液病中的作用和分子功能。最近的发现:成骨细胞谱系已成为HSC扩增的有效调节剂,根据其分化阶段,调节其募集,并沿淋巴系,髓系和红系增殖和分化。此外,成熟成骨细胞或其祖细胞的突变可诱导髓系恶性肿瘤。相反,来自骨髓增生异常细胞的信号可以重塑成骨细胞的生态位,使其有利于自我延续。摘要:了解骨髓微环境中成骨细胞和造血干细胞之间的细胞串扰对开发治疗良恶性血液病的方法具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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