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破骨细胞生成加剧时破骨细胞-成骨祖细胞协调的诱导性外植体模型。

An inducible explant model of osteoclast-osteoprogenitor coordination in exacerbated osteoclastogenesis.

作者信息

Whitlock Jarred M, de Castro Luis F, Collins Michael T, Chernomordik Leonid V, Boyce Alison M

机构信息

Section on Membrane Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

Skeletal Disorders and Mineral Homeostasis Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD20892, USA.

出版信息

iScience. 2023 Mar 23;26(4):106470. doi: 10.1016/j.isci.2023.106470. eCollection 2023 Apr 21.

Abstract

Elucidating a basic blueprint of osteoclast-osteoblast coordination in skeletal remodeling and understanding how this coordination breaks down with age and disease is essential for addressing the growing skeletal health problem in our aging population. The paucity of simple, activatable, biologically relevant models of osteoclast-osteoblast coordination has hindered our understanding of how skeletal remolding is regulated. Here, we describe an inducible model of osteoclast-osteoblast progenitor coordination. Induction activates the release of osteoclastogenic factors from osteoprogenitors, which elicits the differentiation and fusion of neighboring preosteoclasts. In turn, multinucleated osteoclasts release soluble coupling factors, RANK extracellular vesicles and promote osteoprogenitor proliferation, recapitulating aspects of perturbed coordination in diseases underpinned by excessive osteoclast formation. We expect this model to expedite the investigation of cell-cell fusion, osteoclast-osteoblast progenitor coordination, and extracellular vesicle signaling during bone remodeling and offer a powerful tool for evaluating signaling cascades and novel therapeutic interventions in osteoclast-linked skeletal disease.

摘要

阐明骨骼重塑过程中破骨细胞-成骨细胞协调的基本蓝图,并了解这种协调如何随着年龄增长和疾病而瓦解,对于解决老龄化人口中日益严重的骨骼健康问题至关重要。缺乏简单、可激活、具有生物学相关性的破骨细胞-成骨细胞协调模型阻碍了我们对骨骼重塑调控方式的理解。在此,我们描述了一种破骨细胞-成骨细胞祖细胞协调的诱导模型。诱导激活了骨祖细胞中破骨细胞生成因子的释放,这引发了相邻前破骨细胞的分化和融合。反过来,多核破骨细胞释放可溶性偶联因子、RANK细胞外囊泡并促进骨祖细胞增殖,概括了由破骨细胞过度形成所导致的疾病中协调紊乱的各个方面。我们期望这个模型能够加速对骨重塑过程中细胞-细胞融合、破骨细胞-成骨细胞祖细胞协调以及细胞外囊泡信号传导的研究,并为评估破骨细胞相关骨骼疾病中的信号级联反应和新型治疗干预提供一个强大的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d063/10119607/4f00cb61dd4a/fx1.jpg

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