Chen Hung-Lin, Chiang Po-Cheng, Lo Chia-Hui, Lo Yuan-Hsin, Hsu Daniel K, Chen Huan-Yuan, Liu Fu-Tong
Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Graduate institute of immunology, College of Medicine, National Taiwan University, Taipei, Taiwan.
J Invest Dermatol. 2016 Jan;136(1):182-191. doi: 10.1038/JID.2015.366.
Galectin-7, a member of the β-galactoside-binding protein family, is primarily expressed in stratified epithelial cells, including keratinocytes. There is information in the literature suggesting a role for this protein in regulation of keratinocyte survival and growth, but the underlying mechanism remains relatively unknown. Moreover, its expression pattern in the epidermis suggests that it is also involved in the regulation of keratinocyte differentiation. Here, we demonstrate that galectin-7 knockdown results in reduced differentiation and increased proliferation of keratinocytes. Using microarray and deep-sequencing analyses, we found that galectin-7 positively and negatively regulates microRNA (miR)-203 and miR-146a expression, respectively. We show that galectin-7 regulates keratinocyte differentiation and proliferation through miR-203 but not miR-146a. A knockdown of either galectin-7 or miR-203 in keratinocytes increases expression of p63, an essential transcription factor involved in skin development. Rescue of miR-203 expression in a galectin-7 knockdown model reduces p63 expression to baseline. Increased galectin-7 expression upregulates c-Jun N-terminal kinase (JNK) protein levels, which is required for miR-203 expression. Finally, we establish that galectin-7 can be associated with JNK1 and protect it from ubiquitination and degradation. Thus, our data suggest an intracellular function of galectin-7: regulation of keratinocyte proliferation and differentiation through the JNK1-miR-203-p63 pathway.
半乳糖凝集素-7是β-半乳糖苷结合蛋白家族的成员之一,主要在包括角质形成细胞在内的复层上皮细胞中表达。文献中有信息表明该蛋白在调节角质形成细胞的存活和生长中发挥作用,但其潜在机制仍相对未知。此外,其在表皮中的表达模式表明它也参与角质形成细胞分化的调节。在此,我们证明敲低半乳糖凝集素-7会导致角质形成细胞分化减少和增殖增加。通过微阵列和深度测序分析,我们发现半乳糖凝集素-7分别正向和负向调节微小RNA(miR)-203和miR-146a的表达。我们表明半乳糖凝集素-7通过miR-203而非miR-146a调节角质形成细胞的分化和增殖。角质形成细胞中半乳糖凝集素-7或miR-203的敲低会增加p63的表达,p63是参与皮肤发育的必需转录因子。在半乳糖凝集素-7敲低模型中恢复miR-203的表达可将p63表达降低至基线水平。半乳糖凝集素-7表达增加会上调c-Jun氨基末端激酶(JNK)蛋白水平,这是miR-203表达所必需的。最后,我们确定半乳糖凝集素-7可与JNK1结合并保护其免受泛素化和降解。因此,我们的数据表明半乳糖凝集素-7的细胞内功能:通过JNK1-miR-203-p63途径调节角质形成细胞的增殖和分化。