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MDBK细胞对39 kDa蛋白的结合与内吞作用。

Binding and endocytosis of 39 kDa protein by MDBK cells.

作者信息

Vettenranta K, Bu G, Schwartz A L

机构信息

Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

J Cell Physiol. 1995 Aug;164(2):441-7. doi: 10.1002/jcp.1041640225.

Abstract

A 39 kDa protein copurifies with the low density lipoprotein receptor-related protein (LRP) and regulates ligand interactions with LRP. In our recent studies on the clearance of the 39 kDa protein in vivo, we demonstrated that once the liver LRP receptors were saturated, the kidney became the major organ responsible for the 39 kDa protein clearance (Warshawsky et al., 1993, J. Clin. Invest., 92:937-944). The current study was undertaken in order to investigate the potential binding and cellular processing of the 39 kDa protein by kidney-derived MDBK cells. Herein we demonstrate specific, high-affinity, saturable, and Ca(2+)-dependent binding of the 125I-39 kDa protein to MDBK cells (Kd approximately 10-15 nM, 50-70,000 binding sites per cell). Cellular uptake and degradation of the 125I-39 kDa protein by MDBK cells was also demonstrated with kinetics typical of receptor-mediated endocytosis. Using chemical crosslinking we show that LRP in part mediates the binding of 125I-39 kDa protein to the MDBK cell surface. In addition, the presence of functional LRP on the MDBK cell surface was confirmed by the specific binding of activated alpha 2-macroglobulin, another ligand of LRP. Our data thus demonstrate the ability of kidney-derived MDBK cells to specifically bind, endocytose, and degrade the 39 kDa protein.

摘要

一种39 kDa的蛋白质与低密度脂蛋白受体相关蛋白(LRP)共同纯化,并调节配体与LRP的相互作用。在我们最近关于体内39 kDa蛋白质清除的研究中,我们证明一旦肝脏LRP受体饱和,肾脏就成为负责39 kDa蛋白质清除的主要器官(Warshawsky等人,1993年,《临床研究杂志》,92:937 - 944)。进行当前这项研究是为了调查肾源MDBK细胞对39 kDa蛋白质的潜在结合和细胞处理情况。在此我们证明125I标记的39 kDa蛋白质与MDBK细胞具有特异性、高亲和力、可饱和且依赖Ca(2+)的结合(解离常数约为10 - 15 nM,每个细胞有50 - 70,000个结合位点)。MDBK细胞对125I标记的39 kDa蛋白质的细胞摄取和降解也通过受体介导的内吞作用的典型动力学得以证明。使用化学交联我们表明LRP部分介导了125I标记的39 kDa蛋白质与MDBK细胞表面的结合。此外,通过LRP的另一种配体活化α2 - 巨球蛋白的特异性结合,证实了MDBK细胞表面存在功能性LRP。因此,我们的数据证明了肾源MDBK细胞具有特异性结合、内吞和降解39 kDa蛋白质的能力。

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