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破骨细胞液泡H(+) -ATP酶B亚基的特性分析

Characterization of the osteoclast vacuolar H(+)-ATPase B-subunit.

作者信息

Bartkiewicz M, Hernando N, Reddy S V, Roodman G D, Baron R

机构信息

Department of Cell Biology, Yale University School of Medicine, New Haven, CT 06520-8044, USA.

出版信息

Gene. 1995 Jul 28;160(2):157-64. doi: 10.1016/0378-1119(95)00228-x.

Abstract

During bone resorption, osteoclasts acidify the extracellular bone resorbing compartment via a vacuolar H(+)-ATPase (V-ATPase), which resides in the ruffled-border membrane. In an effort to characterize the composition of the osteoclast V-ATPase catalytic domain, we have isolated a cDNA clone that encodes the V-ATPase B-subunit from a cDNA library constructed from highly purified chicken osteoclasts. Comparison of the predicted amino-acid sequence with the published sequences of isoforms of V-ATPase B-subunits from other sources revealed that the chicken osteoclast B-subunit is brain type and not kidney type. Furthermore, only clones encoding the brain type isoform of subunit B could be generated by PCR from a cDNA library prepared from human osteoclastoma osteoclast-like cells. Northern blot analysis revealed that two B-subunit mRNAs, approx. 1.7 and 3.5 kb in length, are expressed in chicken bone marrow mono-nuclear cells, brain and kidney, although the relative amounts of these two transcripts were different in each tissue. In brain, the 3.5-kb mRNA was predominantly expressed. In bone marrow cells, the levels of the 1.7-kb mRNA were higher than in other tissues and expression of this message was increased by 1,25-dihydroxyvitamin D-3, suggesting that this mRNA is specifically upregulated during osteoclast differentiation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在骨吸收过程中,破骨细胞通过位于皱褶缘膜上的液泡型H(+)-ATP酶(V-ATP酶)使细胞外骨吸收区酸化。为了确定破骨细胞V-ATP酶催化结构域的组成,我们从由高度纯化的鸡破骨细胞构建的cDNA文库中分离出一个编码V-ATP酶B亚基的cDNA克隆。将预测的氨基酸序列与其他来源的V-ATP酶B亚基同工型的已发表序列进行比较,发现鸡破骨细胞B亚基是脑型而非肾型。此外,从人骨巨细胞瘤破骨细胞样细胞制备的cDNA文库中通过PCR只能产生编码亚基B脑型同工型的克隆。Northern印迹分析显示,有两种B亚基mRNA,长度约为1.7和3.5 kb,在鸡骨髓单核细胞、脑和肾中表达,尽管这两种转录本在每个组织中的相对量不同。在脑中,主要表达3.5 kb的mRNA。在骨髓细胞中,1.7 kb mRNA的水平高于其他组织,并且该信息的表达在1,25-二羟维生素D-3作用下增加,表明该mRNA在破骨细胞分化过程中特异性上调。(摘要截短于250字)

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