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调控造血祖细胞的增殖和存活:成骨细胞的参与。

Regulation of haematopoietic progenitor cell proliferation and survival: The involvement of the osteoblast.

机构信息

Academic Unit of Clinical Oncology, School of Medicine and Biomedical Sciences, University of Sheffield, Sheffield, UK.

出版信息

Cell Adh Migr. 2010 Jan-Mar;4(1):4-6. doi: 10.4161/cam.4.1.10106. Epub 2010 Jan 17.

Abstract

Haematopoietic progenitor cells (HPC) traffic between the circulation and the bone marrow. Through contact with osteoblasts in the bone marrow niche, their survival, maintenance and proliferation is regulated. This review summarizes recent observations regarding the interaction between osteoblasts and HPCs, and the resulting downstream effects on signaling and niche maintenance. Using live imaging, amongst other techniques, HPCs were found to make prolonged contact with the osteoblast, via a specialized region of their membrane with high expression of prominin 1, CD63 and rhodamine PE. Following contact, portions of the HPC membrane expressing these molecules were phagocytosed by the osteoblast into SARA-positive signaling-endosomes. In response, Smad signaling was downregulated in the osteoblasts, leading to increased production of SDF-1; a chemokine involved in progenitor cell homing to the bone marrow, and thus regulating progenitor cell trafficking. The study summarised here presents important findings regarding progenitor cell trafficking, maintenance, proliferation and survival in the bone marrow and potentially other niche microenvironments, following signaling events initiated and propagated through single cell interactions.

摘要

造血祖细胞(HPC)在血液循环和骨髓之间迁移。通过与骨髓龛中的成骨细胞接触,它们的存活、维持和增殖受到调节。这篇综述总结了最近关于成骨细胞与 HPC 相互作用的观察结果,以及对信号转导和龛维持的后续影响。使用活体成像等技术,研究人员发现 HPC 通过其膜上高表达 prominin 1、CD63 和 rhodamine PE 的特定区域与成骨细胞进行长时间接触。接触后,表达这些分子的 HPC 膜的一部分被成骨细胞吞噬到 SARA 阳性信号内体中。作为回应,成骨细胞中的 Smad 信号被下调,导致 SDF-1 的产生增加;SDF-1 是一种趋化因子,参与祖细胞归巢到骨髓,从而调节祖细胞的迁移。本文总结了重要的发现,即信号事件通过单细胞相互作用引发和传播后,骨髓和潜在的其他龛微环境中的祖细胞迁移、维持、增殖和存活。

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