Department of Biology, Institute of Molecular Health Sciences, ETH Zurich, 8093 Zurich, Switzerland.
Laboratory of Cancer Genomics, Fondazione Edo ed Elvo Tempia, 13900 Biella, Italy.
Nat Commun. 2014 Oct 6;5:5099. doi: 10.1038/ncomms6099.
The Nrf2 transcription factor controls the expression of genes involved in the antioxidant defense system. Here, we identified Nrf2 as a novel regulator of desmosomes in the epidermis through the regulation of microRNAs. On Nrf2 activation, expression of miR-29a and miR-29b increases in cultured human keratinocytes and in mouse epidermis. Chromatin immunoprecipitation identified the Mir29ab1 and Mir29b2c genes as direct Nrf2 targets in keratinocytes. While binding of Nrf2 to the Mir29ab1 gene activates expression of miR-29a and -b, the Mir29b2c gene is silenced by DNA methylation. We identified desmocollin-2 (Dsc2) as a major target of Nrf2-induced miR-29s. This is functionally important, since Nrf2 activation in keratinocytes of transgenic mice causes structural alterations of epidermal desmosomes. Furthermore, the overexpression of miR-29a/b or knockdown of Dsc2 impairs the formation of hyper-adhesive desmosomes in keratinocytes, whereas Dsc2 overexpression has the opposite effect. These results demonstrate that a novel Nrf2-miR-29-Dsc2 axis controls desmosome function and cutaneous homeostasis.
Nrf2 转录因子控制参与抗氧化防御系统的基因的表达。在这里,我们通过调节 microRNAs 鉴定 Nrf2 为表皮桥粒的新型调节剂。在 Nrf2 激活后,培养的人角质形成细胞和小鼠表皮中 miR-29a 和 miR-29b 的表达增加。染色质免疫沉淀鉴定出 Mir29ab1 和 Mir29b2c 基因为角质形成细胞中 Nrf2 的直接靶基因。虽然 Nrf2 与 Mir29ab1 基因结合可激活 miR-29a 和 miR-29b 的表达,但 Mir29b2c 基因被 DNA 甲基化沉默。我们鉴定出桥粒芯胶蛋白 2(Dsc2)为 Nrf2 诱导的 miR-29 的主要靶标。这在功能上很重要,因为转基因小鼠角质形成细胞中 Nrf2 的激活会导致表皮桥粒的结构改变。此外,miR-29a/b 的过表达或 Dsc2 的敲低会损害角质形成细胞中超粘性桥粒的形成,而 Dsc2 的过表达则有相反的效果。这些结果表明,一种新型的 Nrf2-miR-29-Dsc2 轴控制桥粒功能和皮肤稳态。