The epithelial zinc transporter ZIP10 epigenetically regulates human epidermal homeostasis by modulating histone acetyltransferase activity

被引:22
作者
Bin, B. -H. [1 ,3 ]
Lee, S. -H. [4 ]
Bhin, J. [5 ]
Irie, T. [6 ,7 ]
Kim, S. [4 ]
Seo, J. [2 ]
Mishima, K. [6 ]
Lee, T. R. [1 ]
Hwang, D. [8 ]
Fukada, T. [9 ]
Cho, E. -G. [1 ]
机构
[1] AmorePacific R&D Unit, Basic Res & Innovat Div, Yongin 17014, South Korea
[2] AmorePacific R&D Unit, Beauty Longev Sci Res Div, Yongin 17014, South Korea
[3] Ajou Univ, Dept Biol Sci, Suwon 16499, South Korea
[4] Biosolut Corp, Seoul 01811, South Korea
[5] Netherlands Canc Inst, Div Mol Carcinogenesis, NL-1066 CX Amsterdam, Netherlands
[6] Showa Univ, Div Pathol, Dept Oral Diagnost Sci, Sch Dent, Tokyo 1428666, Japan
[7] Iwate Med Univ, Div Anat & Cellular Pathol, Dept Pathol, Morioka, Iwate 0283694, Japan
[8] Inst Basic Sci, Ctr Syst Biol Plant Senescence & Life Hist, Daegu 42988, South Korea
[9] Tokushima Bunri Univ, Fac Pharmaceut Sci, Tokushima 7708055, Japan
关键词
GENE-EXPRESSION; PROTEIN; DIFFERENTIATION; IDENTIFICATION; DEFICIENCY; HEALTH; FAMILY;
D O I
10.1111/bjd.17339
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background The skin is the first organ that manifests changes in response to zinc deficiency. However, the molecular mechanism underlying how zinc is involved in skin homeostasis, especially its epigenetic regulation, is largely unknown. Objectives In this study we demonstrate the importance of zinc levels and the zinc transporter ZIP10 in the epigenetic maintenance of human epidermal homeostasis. Methods Adult human skin, including skin appendages, were stained with anti-ZIP10 antibody. Histone acetyltransferase (HAT) activity was assessed after treating human keratinocytes with ZIP10 small interfering (si)RNAs or the zinc chelator TPEN. ZIP10- or HAT-regulated genes were analysed based on limma bioinformatics analysis for keratinocytes treated with ZIP10 siRNAs or a HAT inhibitor, or using a public database for transcription factors. A reconstituted human skin model was used to validate the role of ZIP10 in epidermal differentiation and the functional association between ZIP10 and HAT. Results ZIP10 is predominantly expressed in the interfollicular epidermis, epidermal appendages and hair follicles. ZIP10 depletion resulted in epidermal malformations in a reconstituted human skin model via downregulation of the activity of the epigenetic enzyme HAT. This decreased HAT activity, resulting from either ZIP10 depletion or treatment with the zinc chelator TPEN, was readily restored by zinc supplementation. Through bioinformatics analysis for gene sets regulated by knockdown of SLC39A10 (encoding ZIP10) and HAT inhibition, we demonstrated that ZIP10 and HATs were closely linked with the regulation of genes related to epidermal homeostasis, particularly filaggrin and metallothionein. Conclusions Our study suggests that ZIP10-mediated zinc distribution is crucial for epidermal homeostasis via HATs. Therefore, zinc-dependent epigenetic regulation could provide alternatives to maintaining healthy skin or alleviating disorders with skin barrier defects.
引用
收藏
页码:869 / 880
页数:12
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