破骨细胞通过多种机制向成骨细胞系细胞提供耦合信号。

IF 15.7 1区 医学 Q1 PHYSIOLOGY
N. Sims, T. Martin
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引用次数: 125

摘要

骨重建对于受损和陈旧骨的修复和替换至关重要。这一过程的主要原理是破骨细胞介导的大量骨吸收之后是成骨细胞前体的募集;这些细胞分化为产生基质的成骨细胞,形成新的骨来取代被吸收的骨。来自骨硬化综合征的证据表明,破骨细胞不仅吸收骨,而且提供促进骨形成的信号。破骨细胞通过促进生长因子从吸收基质中释放、产生分泌蛋白和微泡以及表达膜结合因子,在成骨细胞的整个分化过程中作用于成骨细胞谱系细胞。这些多重机制介导骨形成与重塑中的吸收的耦合。破骨细胞与成骨细胞谱系细胞的额外相互作用,包括与冠细胞和逆转细胞的相互作用,需要在骨重塑过程中实现骨形成和吸收之间的协调。《生理学年度评论》第82卷预计最终在线出版日期为2020年2月10日。请参阅http://www.annualreviews.org/page/journal/pubdates用于修订估算。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Osteoclasts Provide Coupling Signals to Osteoblast Lineage Cells Through Multiple Mechanisms.
Bone remodeling is essential for the repair and replacement of damaged and old bone. The major principle underlying this process is that osteoclast-mediated resorption of a quantum of bone is followed by osteoblast precursor recruitment; these cells differentiate to matrix-producing osteoblasts, which form new bone to replace what was resorbed. Evidence from osteopetrotic syndromes indicate that osteoclasts not only resorb bone, but also provide signals to promote bone formation. Osteoclasts act upon osteoblast lineage cells throughout their differentiation by facilitating growth factor release from resorbed matrix, producing secreted proteins and microvesicles, and expressing membrane-bound factors. These multiple mechanisms mediate the coupling of bone formation to resorption in remodeling. Additional interactions of osteoclasts with osteoblast lineage cells, including interactions with canopy and reversal cells, are required to achieve coordination between bone formation and resorption during bone remodeling. Expected final online publication date for the Annual Review of Physiology, Volume 82 is February 10, 2020. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.
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来源期刊
Annual review of physiology
Annual review of physiology 医学-生理学
CiteScore
35.60
自引率
0.00%
发文量
41
期刊介绍: Since 1939, the Annual Review of Physiology has been highlighting significant developments in animal physiology. The journal covers diverse areas, including cardiovascular physiology, cell physiology, ecological, evolutionary, and comparative physiology, endocrinology, gastrointestinal physiology, neurophysiology, renal and electrolyte physiology, respiratory physiology, and special topics.
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