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巨噬细胞极化与骨形成:综述

Macrophage Polarization and Bone Formation: A review.

作者信息

Horwood Nicole J

机构信息

Kennedy Institute of Rheumatology, NDORMS, University of Oxford, Roosevelt Drive, Oxford, OX3 7FY, UK.

出版信息

Clin Rev Allergy Immunol. 2016 Aug;51(1):79-86. doi: 10.1007/s12016-015-8519-2.

Abstract

The contribution of inflammation to bone loss is well documented in arthritis and other diseases with an emphasis on how inflammatory cytokines promote osteoclastogenesis. Macrophages are the major producers of cytokines in inflammation, and the factors they produce depend upon their activation state or polarization. In recent years, it has become apparent that macrophages are also capable of interacting with osteoblasts and their mesenchymal precursors. This interaction provides growth and differentiation factors from one cell that act on the other and visa versa-a concept akin to the requirement for a feeder layer to grow hemopoietic cells or the coupling that occurs between osteoblasts and osteoclasts to maintain bone homeostasis. Alternatively, activated macrophages are the most likely candidates to promote bone formation and have also been implicated in the tissue repair process in other tissues. In bone, a number of factors, including oncostatin M, have been shown to promote osteoblast formation both in vitro and in vivo. This review discusses the different cell types involved, cellular mediators, and how this can be used to direct new bone anabolic approaches.

摘要

炎症对骨质流失的影响在关节炎和其他疾病中已有充分记载,重点在于炎性细胞因子如何促进破骨细胞生成。巨噬细胞是炎症中细胞因子的主要产生者,它们产生的因子取决于其激活状态或极化情况。近年来,越来越明显的是巨噬细胞也能够与成骨细胞及其间充质前体细胞相互作用。这种相互作用提供了来自一个细胞的生长和分化因子作用于另一个细胞,反之亦然——这一概念类似于培养造血细胞所需的饲养层,或成骨细胞与破骨细胞之间为维持骨稳态而发生的耦合。另外,活化的巨噬细胞是促进骨形成的最可能候选者,并且也与其他组织的组织修复过程有关。在骨骼中,包括制瘤素M在内的多种因子已被证明在体外和体内均可促进成骨细胞形成。本综述讨论了所涉及的不同细胞类型、细胞介质,以及如何利用这些来指导新的骨合成代谢方法。

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