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破骨细胞谱系与功能。

Osteoclast lineage and function.

作者信息

Väänänen H Kalervo, Laitala-Leinonen Tiina

机构信息

Department of Anatomy, Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, FI-20520, Turku, Finland.

出版信息

Arch Biochem Biophys. 2008 May 15;473(2):132-8. doi: 10.1016/j.abb.2008.03.037. Epub 2008 Apr 6.

Abstract

Osteoclasts are members of the monocyte/macrophage lineage and are formed by cellular fusions from their mononuclear precursors. Their differentiation is regulated by a number of other cells and their products, especially by RANKL and M-CSF. The resorbing osteoclasts are polarized and show specific plasma membrane domains. Polarization and bone resorption need a continuous membrane trafficking and modulation of the cytoskeleton. The most characteristic feature of osteoclasts is their unique capacity to dissolve crystalline hydroxyapatite by targeted secretion of HCl into the extracellular resorption lacuna. Organic matrix is degraded by enzymes like cathepsin K and the degradation products are transcytosed through the cell for secretion. Dissolution of hydroxyapatite releases large amounts of soluble calcium, phosphate and bicarbonate. Removal of these ions apparently involves the vesicular pathways and direct ion transport via different ion exchangers, channels and pumps. Detailed molecular knowledge of osteoclast differentiation and function has helped us to identify several target molecules and develop specific treatments to inhibit pathological bone resorption in various skeletal diseases.

摘要

破骨细胞是单核细胞/巨噬细胞谱系的成员,由其单核前体细胞通过细胞融合形成。它们的分化受许多其他细胞及其产物的调节,尤其是受RANKL和M-CSF的调节。正在进行骨吸收的破骨细胞是极化的,并显示出特定的质膜结构域。极化和骨吸收需要持续的膜运输和细胞骨架的调节。破骨细胞最显著的特征是它们具有独特的能力,即通过将HCl定向分泌到细胞外吸收腔隙中来溶解结晶性羟基磷灰石。有机基质被组织蛋白酶K等酶降解,降解产物通过细胞进行跨细胞转运以分泌。羟基磷灰石的溶解会释放大量可溶性钙、磷酸盐和碳酸氢盐。这些离子的清除显然涉及囊泡途径以及通过不同离子交换器、通道和泵的直接离子运输。对破骨细胞分化和功能的详细分子认识帮助我们确定了几个靶分子,并开发出了在各种骨骼疾病中抑制病理性骨吸收的特异性治疗方法。

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