Galán-Díez Marta, Kousteni Stavroula
Department of Physiology & Cellular Biophysics, College of Physicians & Surgeons, Columbia University, New York, New York 10032, USA.
Curr Mol Biol Rep. 2017 Jun;3(2):53-62. doi: 10.1007/s40610-017-0055-9. Epub 2017 May 2.
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.
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.
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.
本综述着重于突出造血干细胞(HSC)与其周围基质细胞之间双向相互作用的证据,特别强调成骨细胞谱系的细胞。讨论了成骨细胞在正常造血和髓系血液系统恶性肿瘤中的作用及分子功能。
成骨细胞谱系的细胞已成为HSC扩增的有效调节因子,可调节其募集,并根据其分化阶段调节其在淋巴系、髓系和红系谱系中的活性、增殖和分化。此外,成熟成骨细胞或其祖细胞中的突变会诱发髓系恶性肿瘤。相反,骨髓增生异常细胞发出的信号可重塑成骨细胞龛,以利于自我延续。
了解骨髓微环境中骨细胞与HSC之间的细胞相互作用对于开发针对良性和恶性血液疾病的治疗方法至关重要。