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长骨破骨细胞比颅骨破骨细胞表现出增强的破骨细胞表型。

Long bone osteoclasts display an augmented osteoclast phenotype compared to calvarial osteoclasts.

机构信息

Department of Laboratory Medicine, Division of Pathology, Karolinska Institutet, F46 Karolinska University Hospital, Huddinge SE-141 86, Sweden.

出版信息

Biochem Biophys Res Commun. 2010 Apr 9;394(3):743-9. doi: 10.1016/j.bbrc.2010.03.063. Epub 2010 Mar 15.

Abstract

Osteoclasts are multinucleated cells specialized in degrading bone and characterized by high expression of the enzymes tartrate-resistant acid phosphatase (TRAP) and cathepsin K (CtsK). Recent studies show that osteoclasts exhibit phenotypic differences depending on their anatomical site of action. Using immunohistochemistry, RT-qPCR, FPLC chromatography and immunoblotting, we compared TRAP expression in calvaria and long bone. TRAP protein and enzyme activity levels were higher in long bones compared to calvaria. In addition, proteolytic processing of TRAP was more extensive in long bones than calvaria which correlated with higher cysteine proteinase activity and protein expression of CtsK. These two types of bones also exhibited a differential expression of monomeric TRAP and CtsK isoforms. Analysis of CtsK(-/-) mice revealed that CtsK is involved in proteolytic processing of TRAP in calvaria. Moreover, long bone osteoclasts exhibited higher expression of not only TRAP and CtsK but also of the membrane markers CD68 and CD163. The results suggest that long bone osteoclasts display an augmented osteoclastic phenotype with stronger expression of both membranous and secreted osteoclast proteins.

摘要

破骨细胞是专门降解骨骼的多核细胞,其特征是高水平表达抗酒石酸酸性磷酸酶(TRAP)和组织蛋白酶 K(CtsK)等酶。最近的研究表明,破骨细胞根据其作用的解剖部位表现出不同的表型。我们通过免疫组织化学、RT-qPCR、FPLC 色谱和免疫印迹比较了颅骨和长骨中 TRAP 的表达。与颅骨相比,长骨中的 TRAP 蛋白和酶活性水平更高。此外,长骨中 TRAP 的蛋白水解加工比颅骨更广泛,这与更高的半胱氨酸蛋白酶活性和 CtsK 的蛋白表达相关。这两种类型的骨骼还表现出单体 TRAP 和 CtsK 同工型的差异表达。对 CtsK(-/-)小鼠的分析表明,CtsK 参与了颅骨中 TRAP 的蛋白水解加工。此外,长骨破骨细胞不仅表达更高水平的 TRAP 和 CtsK,还表达膜标记物 CD68 和 CD163。这些结果表明,长骨破骨细胞表现出增强的破骨细胞表型,表达更多的膜结合和分泌型破骨细胞蛋白。

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