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参与破骨细胞与骨非细胞成分结合和反应的质膜受体。

Plasma Membrane Receptors Involved in the Binding and Response of Osteoclasts to Noncellular Components of the Bone.

机构信息

Department of Orthodontics, College of Dentistry, University of Florida, Gainesville, FL 32610, USA.

Department of Anatomy & Cell Biology, College of Medicine, University of Florida, Gainesville, FL 32610, USA.

出版信息

Int J Mol Sci. 2021 Sep 18;22(18):10097. doi: 10.3390/ijms221810097.

Abstract

Osteoclasts differentiate from hematopoietic cells and resorb the bone in response to various signals, some of which are received directly from noncellular elements of the bone. In vitro, adherence to the bone triggers the reduction of cell-cell fusion events between osteoclasts and the activation of osteoclasts to form unusual dynamic cytoskeletal and membrane structures that are required for degrading the bone. Integrins on the surface of osteoclasts are known to receive regulatory signals from the bone matrix. Regulation of the availability of these signals is accomplished by enzymatic alterations of the bone matrix by protease activity and phosphorylation/dephosphorylation events. Other membrane receptors are present in osteoclasts and may interact with as yet unidentified signals in the bone. Bone mineral has been shown to have regulatory effects on osteoclasts, and osteoclast activity is also directly modulated by mechanical stress. As understanding of how osteoclasts and other bone cells interact with the bone has emerged, increasingly sophisticated efforts have been made to create bone biomimetics that reproduce both the structural properties of the bone and the bone's ability to regulate osteoclasts and other bone cells. A more complete understanding of the interactions between osteoclasts and the bone may lead to new strategies for the treatment of bone diseases and the production of bone biomimetics to repair defects.

摘要

破骨细胞起源于造血细胞,能够响应各种信号而分解骨组织,其中一些信号直接来自于骨的非细胞成分。在体外,破骨细胞与骨的黏附会触发细胞-细胞融合事件减少,并激活破骨细胞形成独特的动态细胞骨架和膜结构,这是降解骨组织所必需的。已知破骨细胞表面的整合素可以接收来自骨基质的调节信号。通过蛋白酶活性和磷酸化/去磷酸化事件对骨基质进行酶促改变,从而实现这些信号可用性的调节。破骨细胞中还存在其他膜受体,它们可能与骨中尚未识别的信号相互作用。已经证明骨矿物质对破骨细胞具有调节作用,机械应力也直接调节破骨细胞的活性。随着人们对破骨细胞和其他骨细胞如何与骨相互作用的理解不断深入,人们越来越努力地创造骨仿生材料,以复制骨的结构特性及其调节破骨细胞和其他骨细胞的能力。对破骨细胞与骨之间相互作用的更全面理解可能会为治疗骨疾病和生产修复缺陷的骨仿生材料提供新的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/057e/8466431/11a59c0e3a8e/ijms-22-10097-g002.jpg

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