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破骨细胞在骨骼发育、稳态和修复中的起源和作用。

The origins and roles of osteoclasts in bone development, homeostasis and repair.

机构信息

Department of Orthopaedic Surgery, Duke University School of Medicine, Durham, NC 27710, United States.

Department of Molecular and Medical Pharmacology, Faculty of Medicine, University of Toyama, Toyama, 930-0194, Japan.

出版信息

Development. 2022 Apr 15;149(8). doi: 10.1242/dev.199908. Epub 2022 May 3.

DOI:10.1242/dev.199908
PMID:35502779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9124578/
Abstract

The mechanisms underlying bone development, repair and regeneration are reliant on the interplay and communication between osteoclasts and other surrounding cells. Osteoclasts are multinucleated monocyte lineage cells with resorptive abilities, forming the bone marrow cavity during development. This marrow cavity, essential to hematopoiesis and osteoclast-osteoblast interactions, provides a setting to investigate the origin of osteoclasts and their multi-faceted roles. This Review examines recent developments in the embryonic understanding of osteoclast origin, as well as interactions within the immune environment to regulate normal and pathological bone development, homeostasis and repair.

摘要

骨发育、修复和再生的机制依赖于破骨细胞和其他周围细胞的相互作用和通讯。破骨细胞是具有吸收能力的多核单核细胞谱系细胞,在发育过程中形成骨髓腔。这个骨髓腔对造血和破骨细胞-成骨细胞相互作用至关重要,为研究破骨细胞的起源及其多方面的作用提供了一个环境。本综述检查了胚胎对破骨细胞起源的理解以及在免疫环境内的相互作用方面的最新进展,以调节正常和病理性骨发育、稳态和修复。

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本文引用的文献

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Aged skeletal stem cells generate an inflammatory degenerative niche.衰老的骨骼干细胞产生炎症性退行性龛位。
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Osteoclasts recycle via osteomorphs during RANKL-stimulated bone resorption.破骨细胞在 RANKL 刺激的骨吸收过程中通过骨形态发生蛋白进行再循环。
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Monocyte/Macrophage Lineage Cells From Fetal Erythromyeloid Progenitors Orchestrate Bone Remodeling and Repair.来自胎儿红系髓系祖细胞的单核细胞/巨噬细胞谱系细胞协调骨骼重塑和修复。
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