Suppr超能文献

破骨细胞极化的调控

Regulation of osteoclast polarization.

作者信息

Takahashi Naoyuki, Ejiri Sadakazu, Yanagisawa Shigeru, Ozawa Hidehiro

机构信息

Institute for Oral Science, Matsumoto Dental University, 1780 Gobara, Hiro-oka, Shiojiri, Nagano, Japan.

出版信息

Odontology. 2007 Jul;95(1):1-9. doi: 10.1007/s10266-007-0071-y. Epub 2007 Jul 25.

Abstract

Osteoclast function consists of several processes: recognition of mineralized tissues, development of ruffled borders and sealing zones, secretion of acids and proteolytic enzymes into the space beneath the ruffled border, and incorporation and secretion of bone degradation products using the transcytosis system. One of the most important questions concerning osteoclast function is how osteoclasts recognize bone and polarize. During the past decade, new approaches have been taken to investigate the regulation of osteoclast polarization. Attachment of osteoclasts to some proteins containing the Arg-Gly-Asp sequence motif through vitronectin receptors is the first step in inducing the polarization of osteoclasts. Physical properties of bone such as hardness or roughness are also required to induce osteoclast polarity. Osteoclasts cultured even on plastic dishes secrete protons toward the dish surface, suggesting that osteoclasts recognize plastic as a mineralized matrix and secrete protons. This notion was supported by the recent findings that bisphosphonates and reveromycin A were specifically incorporated into polarized osteoclasts cultured even on plastic dishes. On the other hand, a sealing zone, defined as a thick band of actin, is induced in osteoclasts adherent only on an apatite-containing mineralized matrix. These results suggest that osteoclasts recognize physical properties of the mineralized tissue to secrete protons, and also sense apatite itself or components of apatite to form the sealing zone. Here, we review recent findings on the regulation of osteoclast polarization. We also discuss how osteoclasts recognize mineralized tissues to form the sealing zone.

摘要

破骨细胞的功能包括几个过程

识别矿化组织、形成褶皱边缘和封闭区、将酸和蛋白水解酶分泌到褶皱边缘下方的空间,以及利用转胞吞系统摄取和分泌骨降解产物。关于破骨细胞功能的最重要问题之一是破骨细胞如何识别骨骼并极化。在过去十年中,人们采用了新的方法来研究破骨细胞极化的调节。破骨细胞通过玻连蛋白受体与一些含有精氨酸-甘氨酸-天冬氨酸序列基序的蛋白质结合是诱导破骨细胞极化的第一步。骨骼的物理特性,如硬度或粗糙度,也需要诱导破骨细胞极性。即使在塑料培养皿上培养的破骨细胞也会向培养皿表面分泌质子,这表明破骨细胞将塑料识别为矿化基质并分泌质子。双膦酸盐和瑞伐霉素A即使在塑料培养皿上培养的极化破骨细胞中也能特异性结合,这一最新发现支持了这一观点。另一方面,仅在含磷灰石的矿化基质上黏附的破骨细胞中会诱导形成一个由肌动蛋白组成的厚带,即封闭区。这些结果表明,破骨细胞识别矿化组织的物理特性以分泌质子,并且还感知磷灰石本身或磷灰石的成分以形成封闭区。在这里,我们综述了关于破骨细胞极化调节的最新发现。我们还讨论了破骨细胞如何识别矿化组织以形成封闭区。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验