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小鼠层粘连蛋白γ2(B2t)链的克隆与表达,上皮细胞层粘连蛋白的一个亚基

Cloning and expression of the mouse laminin gamma 2 (B2t) chain, a subunit of epithelial cell laminin.

作者信息

Sugiyama S, Utani A, Yamada S, Kozak C A, Yamada Y

机构信息

Laboratory of Developmental Biology, National Institute of Dental Research, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Eur J Biochem. 1995 Feb 15;228(1):120-8. doi: 10.1111/j.1432-1033.1995.tb20239.x.

Abstract

We have isolated and sequenced the full-length cDNA for the mouse laminin gamma 2 chain and mapped it to mouse Chromosome 1 proximal to laminin gamma 1. The mRNA for the mouse gamma 2 spans 5.2 kb and codes for a 1192-residue amino acid polypeptide. The gamma 2 chain (formerly termed laminin B2t), a homologue of gamma 1 (formerly B2), lacks an N-terminal domain and has a shorter domain III in comparison to the laminin gamma 1 chain. The expression of the laminin gamma 2 and gamma 1 chains in both newborn and fetal mice was examined by both Northern analysis and in situ hybridization. mRNA for the laminin gamma 2 chain was expressed specifically by epithelial cells in many tissues with a particularly high level of expression in the tongue, hair follicles, lung and kidney. In contrast, a high level of expression of the laminin gamma 1 chain mRNA was seen in both epithelial and endothelial cells in these tissues. In addition, gamma 1 mRNA was expressed in other tissues such as the nasal septum, blood vessels, and the muscle of the tongue. Immunohistochemistry with an anti-gamma 2 IgG detected strong expression of the laminin gamma 2 chain in the basement membrane of the collecting tubules of the kidney and of the pancreas. Immunoprecipitation studies with antibodies to the gamma 2 chain detected three species at 165, 155 and 140 kDa in HT-1080 cell-conditioned media. This protein complex is characteristic of the kalinin (nicein/epiligrin) complex, and provides further evidence that these proteins are identical and that the gamma 2 chain is the subunit of the epithelial-cell-specific laminin.

摘要

我们已分离并测序了小鼠层粘连蛋白γ2链的全长cDNA,并将其定位到小鼠1号染色体上靠近层粘连蛋白γ1的位置。小鼠γ2的mRNA跨度为5.2 kb,编码一个1192个氨基酸残基的多肽。γ2链(以前称为层粘连蛋白B2t)是γ1(以前称为B2)的同源物,与层粘连蛋白γ1链相比,它缺少一个N端结构域,且结构域III较短。通过Northern分析和原位杂交检测了层粘连蛋白γ2和γ1链在新生小鼠和胎鼠中的表达情况。层粘连蛋白γ2链的mRNA在许多组织的上皮细胞中特异性表达,在舌、毛囊、肺和肾中表达水平特别高。相比之下,在这些组织的上皮细胞和内皮细胞中均可见层粘连蛋白γ1链mRNA的高水平表达。此外,γ1 mRNA在其他组织如鼻中隔、血管和舌肌中也有表达。用抗γ2 IgG进行免疫组织化学检测发现,层粘连蛋白γ2链在肾集合小管和胰腺的基底膜中有强烈表达。用抗γ2链抗体进行免疫沉淀研究,在HT-1080细胞条件培养基中检测到165、155和140 kDa的三种蛋白。这种蛋白复合物是kalinin(nicein/epiligrin)复合物的特征,进一步证明这些蛋白是相同的,且γ2链是上皮细胞特异性层粘连蛋白的亚基。

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