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首页> 外文期刊>Journal of Cell Science >Identification of the membrane-type matrix metalloproteinase MT1-MMP in osteoclasts.
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Identification of the membrane-type matrix metalloproteinase MT1-MMP in osteoclasts.

机译:破骨细胞中膜型基质金属蛋白酶MT1-MMP的鉴定。

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摘要

The osteoclasts are the cells responsible for bone resorption. Matrix metalloproteinases (MMPs) appear crucial for this process. To identify possible MMP expression in osteoclasts, we amplified osteoclast cDNA fragments having homology with MMP genes, and used them as a probe to screen a rabbit osteoclast cDNA library. We obtained a cDNA of 1,972 bp encoding a polypeptide of 582 amino acids that showed more than 92% identity to human, mouse, and rat membrane-type 1 MMP (MT1-MMP), a cell surface proteinase believed to trigger cancer cell invasion. By northern blotting, MT1-MMP was found to be highly expressed in purified osteoclasts when compared with alveolar macrophages and bone stromal cells, as well as with various tissues. In situ hybridization on bone sections showed that MT1-MMP is expressed also in osteoclasts in vivo. Antibodies recognizing MT1-MMP reacted with specific plasma membrane areas corresponding to lamellipodia and podosomes involved, respectively, in migratory and attachment activities of the osteoclasts. These observations highlight how cells might bring MT1-MMP into contact with focal points of the extracellular matrix, and are compatible with a role of MT1-MMP in migratory and attachment activities of the osteoclast.
机译:破骨细胞是负责骨吸收的细胞。基质金属蛋白酶(MMP)似乎对此过程至关重要。为了鉴定破骨细胞中可能的MMP表达,我们扩增了与MMP基因具有同源性的破骨cDNA片段,并将其用作筛选兔破骨cDNA文库的探针。我们获得了一个1,972 bp的cDNA,编码582个氨基酸的多肽,与人,小鼠和大鼠的1型膜MMP(MT1-MMP)表现出超过92%的同一性,MMP是一种据信会引发癌细胞入侵的细胞表面蛋白酶。通过Northern印迹,与肺泡巨噬细胞和骨基质细胞以及各种组织相比,MT1-MMP被发现在纯化的破骨细胞中高表达。骨切片上的原位杂交表明,MT1-MMP在体内的破骨细胞中也表达。识别MT1-MMP的抗体与特定的质膜区域发生反应,这些区域分别对应于破骨细胞和足小体参与破骨细胞的迁移和附着活动。这些观察结果突出了细胞如何使MT1-MMP与细胞外基质的焦点接触,并与MT1-MMP在破骨细胞的迁移和附着活动中的作用兼容。

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