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造血祖细胞定位于骨髓基质的潜在黏附机制。

Potential adhesion mechanisms for localisation of haemopoietic progenitors to bone marrow stroma.

作者信息

Simmons P J, Zannettino A, Gronthos S, Leavesley D

机构信息

Matthew Roberts Laboratory, Leukaemia Research Unit, Hanson Centre for Cancer Research, Adelaide, South Australia.

出版信息

Leuk Lymphoma. 1994 Feb;12(5-6):353-63. doi: 10.3109/10428199409073776.

Abstract

Haemopoiesis occurs in intimate physical association with the stromal elements of the bone marrow. Current evidence supports the hypothesis that the restriction of primitive haemopoietic progenitor cells (HPC) to the bone marrow involves developmentally regulated adhesive interactions between HPC and the stromal cell microenvironment. This review examines the expression and function of cell adhesion molecules (CAM) on human HPC and marrow stromal cells. These data demonstrate that a broad range of CAMs representing at least three adhesion molecule superfamilies (integrins, selectins, immunoglobulin gene superfamily) participate in these adhesive interactions. We discuss the potential contribution of these various adhesion molecules to homing of HPC to the bone marrow, their retention within the extravascular haemopoietic compartment and their egress into the peripheral circulation. It is likely that each process is mediated not by a single binding event but requires the coordinated participation of multiple receptor-ligand pairs.

摘要

造血过程与骨髓的基质成分密切相关。目前的证据支持这样一种假说,即原始造血祖细胞(HPC)定位于骨髓涉及HPC与基质细胞微环境之间发育调控的黏附相互作用。这篇综述探讨了细胞黏附分子(CAM)在人HPC和骨髓基质细胞上的表达及功能。这些数据表明,代表至少三个黏附分子超家族(整合素、选择素、免疫球蛋白基因超家族)的多种CAM参与了这些黏附相互作用。我们讨论了这些不同黏附分子对HPC归巢至骨髓、它们在血管外造血隔室内的滞留以及它们进入外周循环的潜在作用。每个过程可能并非由单一的结合事件介导,而是需要多个受体-配体对的协同参与。

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