Sawada Naoki, Taketani Yutaka, Amizuka Norio, Ichikawa Masako, Ogawa Chiharu, Nomoto Kaori, Nashiki Kunitaka, Sato Tadatoshi, Arai Hidekazu, Isshiki Masashi, Segawa Hiroko, Yamamoto Hironori, Miyamoto Ken-Ichi, Takeda Eiji
Department of Clinical Nutrition, Institute of Health Biosciences, University of Tokushima Graduate School, 3-18-15 Kuramoto-cho, Tokushima 770-8503, Japan.
Bone. 2007 Jul;41(1):52-8. doi: 10.1016/j.bone.2007.02.030. Epub 2007 Mar 14.
Caveolin-1 is an essential and signature protein of caveolae, which are small invaginations of the plasma membrane enriched in cholesterol and sphingolipids. Although high levels of expression of caveolin-1 have been demonstrated in osteoblasts as well as endothelial cells, fibroblasts, and muscular cells, the role of caveolin-1 in osteoblasts has not been clarified. Here, we show that caveolin-1 is secreted from osteoblasts in the form of matrix vesicles; extracellular vesicles released from the plasma membrane of osteoblasts. In this study, caveolae and matrix vesicles were similarly enriched in cholesterol and sphingomyelin in fractions isolated from mineralizing MC3T3-E1 cells. Interestingly, in the MC3T3-E1 cells caveolin-1 was enriched in the matrix vesicle fraction as well as the caveolar membrane fraction, and the amount of caveolin-1 in the matrix vesicle fraction increased as differentiation progressed. Localization of caveolin-1 in matrix vesicles was also confirmed in murine tibia. Furthermore, overexpression of caveolin-1 enhanced matrix calcification in MC3T3-E1 cells, whereas knockdown of caveolin-1 diminished it. These results suggest that secreted caveolin-1 as a component of matrix vesicles may play an important role in osteoblast calcification.
小窝蛋白-1是小窝的一种必需且标志性的蛋白质,小窝是富含胆固醇和鞘脂的质膜的小内陷。尽管已证实在成骨细胞以及内皮细胞、成纤维细胞和肌肉细胞中小窝蛋白-1有高水平表达,但小窝蛋白-1在成骨细胞中的作用尚未阐明。在此,我们表明小窝蛋白-1以基质小泡的形式从成骨细胞分泌;基质小泡是从成骨细胞质膜释放的细胞外小泡。在本研究中,从矿化的MC3T3-E1细胞分离的组分中,小窝和基质小泡同样富含胆固醇和鞘磷脂。有趣的是,在MC3T3-E1细胞中,小窝蛋白-1在基质小泡组分以及小窝膜组分中均有富集,并且随着分化进展,基质小泡组分中小窝蛋白-1的量增加。在小鼠胫骨中也证实了小窝蛋白-1在基质小泡中的定位。此外,小窝蛋白-1的过表达增强了MC3T3-E1细胞中的基质钙化,而小窝蛋白-1的敲低则使其减弱。这些结果表明,作为基质小泡成分分泌的小窝蛋白-1可能在成骨细胞钙化中起重要作用。