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小窝蛋白-1和-2的表达在培养的角质形成细胞以及皮肤伤口再生表皮中受到不同的调节。

Caveolin-1 and -2 expression is differentially regulated in cultured keratinocytes and within the regenerating epidermis of cutaneous wounds.

作者信息

Gassmann M G, Werner S

机构信息

Max-Planck-Institute of Biochemistry, Martinsried, Germany.

出版信息

Exp Cell Res. 2000 Jul 10;258(1):23-32. doi: 10.1006/excr.2000.4904.

DOI:10.1006/excr.2000.4904
PMID:10912784
Abstract

Keratinocyte growth factor (KGF) and its receptor are involved in various types of epithelial repair processes. To gain insight into the molecular mechanisms of KGF action in the healing skin wound, we searched for genes which are regulated by this factor in cultured keratinocytes. Using the PCR-select technology we constructed a subtractive cDNA library. One of the KGF-regulated genes that we identified was shown to encode caveolin-1, a major component of caveolar membranes. Caveolin-1 is involved in a wide variety of cellular processes, particularly in the regulation of various signal transduction pathways. Caveolin-1 mRNA levels increased in cultured keratinocytes after KGF treatment. By in situ hybridization and immunohistochemistry we found a strong expression of caveolin-1 in the KGF-responsive basal keratinocytes of the epidermis and the hyperproliferative epithelium of the wound as well as in endothelial cells and in other cells of the granulation tissue. In 13-day wounds expression of caveolin-1 mRNA was restricted to the regenerated dermis. In addition to caveolin-1, the mRNA expression of caveolin-2, a second member of the caveolin family, was also induced in keratinocytes after stimulation with KGF but also with other growth factors and cytokines. In contrast to caveolin-1, caveolin-2 protein was expressed in all layers of the normal epidermis and in the suprabasal layers of the hyperproliferative wound epithelium. These results demonstrate a differential expression of caveolin-1 and -2 in proliferating versus differentiating keratinocytes.

摘要

角质形成细胞生长因子(KGF)及其受体参与多种类型的上皮修复过程。为深入了解KGF在皮肤创伤愈合中作用的分子机制,我们在培养的角质形成细胞中寻找受该因子调控的基因。利用PCR-Select技术,我们构建了一个消减cDNA文库。我们鉴定出的一个受KGF调控的基因被证明编码小窝蛋白-1,它是小窝膜的主要成分。小窝蛋白-1参与多种细胞过程,尤其在各种信号转导途径的调控中。KGF处理后,培养的角质形成细胞中小窝蛋白-1的mRNA水平升高。通过原位杂交和免疫组织化学,我们发现小窝蛋白-1在表皮中对KGF有反应的基底角质形成细胞、伤口的过度增殖上皮以及内皮细胞和肉芽组织的其他细胞中强烈表达。在13天的伤口中,小窝蛋白-1的mRNA表达局限于再生的真皮。除了小窝蛋白-1,小窝蛋白家族的另一个成员小窝蛋白-2的mRNA表达在KGF刺激后也在角质形成细胞中被诱导,其他生长因子和细胞因子刺激后也会如此。与小窝蛋白-1不同,小窝蛋白-2蛋白在正常表皮的所有层以及过度增殖的伤口上皮的基底上层表达。这些结果表明小窝蛋白-1和-2在增殖与分化的角质形成细胞中存在差异表达。

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