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巴弗洛霉素A1对破骨细胞质子转运的抑制作用可消除骨吸收。

Inhibition of osteoclast proton transport by bafilomycin A1 abolishes bone resorption.

作者信息

Sundquist K, Lakkakorpi P, Wallmark B, Väänänen K

机构信息

Department of Anatomy, University of Oulu, Finland.

出版信息

Biochem Biophys Res Commun. 1990 Apr 16;168(1):309-13. doi: 10.1016/0006-291x(90)91709-2.

Abstract

Osteoclasts are the main bone resorbing cells with capacity to acidify their intimate contact area with bone. Recent studies have suggested that osteoclast acid secretion is carried out by an H(+)-ATPase. We demonstrate here, that specific inhibitor of vacuolar type H(+)-ATPases, bafilomycin A1, inhibits bone resorption in osteoclast cultures as well as blocks proton transport in isolated medullary bone derived microsomes containing a vacuolar type H(+)-ATPase. These results demonstrate an important role of vacuolar H(+)-ATPase in bone resorption.

摘要

破骨细胞是主要的骨吸收细胞,能够酸化其与骨紧密接触的区域。最近的研究表明,破骨细胞的酸分泌是由一种H(+)-ATP酶进行的。我们在此证明,液泡型H(+)-ATP酶的特异性抑制剂巴弗洛霉素A1,可抑制破骨细胞培养中的骨吸收,并阻断含有液泡型H(+)-ATP酶的分离骨髓骨衍生微粒体中的质子转运。这些结果证明了液泡H(+)-ATP酶在骨吸收中具有重要作用。

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