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Desmosomal Cadherin Misexpression Alters β-Catenin Stability and Epidermal Differentiation

机译:桥粒钙黏着蛋白表达异常改变β-连环蛋白的稳定性和表皮分化

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摘要

Desmosomal adhesion is important for the integrity and protective barrier function of the epidermis and is disregulated during carcinogenesis. Strong adhesion between keratinocytes is conferred by the desmosomal cadherins, desmocollin (Dsc) and desmoglein. These constitute two gene families, members of which are differentially expressed in epidermal strata. It has been suggested that this stratum-specific expression regulates keratinocyte differentiation. We tested this hypothesis by misdirecting the expression of the basally abundant desmosomal cadherins Dsc3a and Dsc3b to suprabasal differentiating keratinocytes in transgenic mice. No phenotype was apparent until adulthood, when mice developed variable ventral alopecia and had altered keratinocyte differentiation within affected areas. The follicular changes were reminiscent of changes in transgenic mice with an altered β-catenin stability. Stabilized β-catenin and increased β-catenin transcriptional activity were demonstrated in transgenic mice prior to the phenotypic change and in transgenic keratinocytes as a consequence of transgene expression. Hence, a link between desmosomal cadherins and β-catenin stability and signaling was demonstrated, and it was shown that desmocollin cadherin expression can affect keratinocyte differentiation. Furthermore, the first function for a “b-type” desmocollin cadherin was demonstrated.
机译:桥粒附着对于表皮的完整性和保护性屏障功能很重要,并且在致癌过程中被破坏。桥粒钙黏着蛋白,桥粒胶蛋白(Dsc)和桥粒糖蛋白赋予角质形成细胞之间强烈的粘附力。这些构成两个基因家族,其成员在表皮层中差异表达。已经提出,该层特异性表达调节角质形成细胞的分化。我们通过将基础丰富的桥粒钙黏着蛋白Dsc3a和Dsc3b的表达误导到转基因小鼠的基底上分化角质形成细胞中,从而测试了这一假设。直到成年之前,没有表型是明显的,那时小鼠发展出可变的腹侧脱发并改变了受影响区域内的角质形成细胞分化。卵泡变化使人联想到β-catenin稳定性改变的转基因小鼠的变化。由于转基因表达,在表型改变之前在转基因小鼠中和在转基因角质形成细胞中证实了稳定的β-catenin和增加的β-catenin转录活性。因此,证明了桥粒钙黏着蛋白与β-catenin稳定性和信号传导之间的联系,并且表明桥粒钙粘蛋白钙黏着蛋白的表达可以影响角质形成细胞的分化。此外,还展示了“ b型”桥粒胶钙粘蛋白的第一个功能。

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