Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Department of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.
Exp Dermatol. 2019 Nov;28(11):1341-1347. doi: 10.1111/exd.14019. Epub 2019 Sep 4.
Apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like (APOBEC) family consists of deaminases. Some isozymes of APOBEC3 are induced upon human papillomavirus infection or development of psoriasis skin lesions. However, the involvement of APOBEC3 in keratinocyte differentiation has not been addressed. We herein sought to evaluate the roles of APOBECs in mouse primary keratinocyte differentiation. We found that expression levels of APOBEC1 and APOBEC3 were increased during calcium-induced keratinocyte differentiation. Unexpectedly, however, the expression levels of keratinocyte differentiation markers keratin 1/10, involucrin, loricrin and filaggrin were higher in keratinocytes treated with APOBEC3 siRNAs than in those treated with control RNAs. In addition, the treatment of keratinocytes with APOBEC3 siRNAs increased the gene expression levels of Notch3, a master regulator of keratinocyte differentiation. Moreover, calcium-induced increase in Notch3 expression and keratinocyte differentiation were impaired by transfection with an APOBEC3 expression plasmid. Furthermore, co-treatment with Notch3 siRNAs reduced the APOBEC3 siRNA-mediated upregulation of Notch3 expression and in part attenuated the increased expression levels of keratinocyte differentiation markers. These results suggest that APOBEC3 is induced upon keratinocyte differentiation and negatively regulates the keratinocyte differentiation in part by its inhibitory role for Notch3 expression.
载脂蛋白 B mRNA 编辑酶、催化多肽样(APOBEC)家族由脱氨酶组成。一些 APOBEC3 同工酶在人乳头瘤病毒感染或银屑病皮肤损伤发展时被诱导。然而,APOBEC3 参与角质形成细胞分化尚未得到解决。在此,我们试图评估 APOBEC 在小鼠原代角质形成细胞分化中的作用。我们发现,在钙诱导的角质形成细胞分化过程中,APOBEC1 和 APOBEC3 的表达水平增加。然而,令人意外的是,用 APOBEC3 siRNA 处理的角质形成细胞中角质形成细胞分化标志物角蛋白 1/10、内披蛋白、兜甲蛋白和丝聚合蛋白的表达水平高于用对照 RNA 处理的角质形成细胞。此外,用 APOBEC3 siRNA 处理角质形成细胞会增加 Notch3 的基因表达水平,Notch3 是角质形成细胞分化的主要调节因子。此外,APOBEC3 表达质粒的转染会损害钙诱导的 Notch3 表达增加和角质形成细胞分化。此外,共转染 Notch3 siRNA 可降低 APOBEC3 siRNA 介导的 Notch3 表达上调,并部分减弱角质形成细胞分化标志物表达水平的增加。这些结果表明,APOBEC3 在角质形成细胞分化时被诱导,并通过其对 Notch3 表达的抑制作用部分负调控角质形成细胞分化。