Profiling Motility Signal-Specific Genes in Primary Human Keratinocytes

• Published in: Journal of investigative dermatology Vol. 128; no. 8; pp. 1981 - 1990
• Main Authors: Cheng, Chieh-Fang, Fan, Jianhua, Bandyopahdhay, Balaji, Mock, Dennis, Guan, Shengxi, Chen, Mei, Woodley, David T., Li, Wei
• Format: Journal Article
• Language: English
• Published: Danvers, MA Elsevier Inc 01.08.2008; Nature Publishing; Elsevier Limited
• Subjects: Biological and medical sciences; Cell Movement - genetics; Cell Proliferation; Cells, Cultured; Dermatology; Down-Regulation - physiology; Gene Expression Profiling; Genes, Immediate-Early - genetics; Humans; Insulin - physiology; Keratinocytes - cytology; Medical sciences; Signal Transduction - genetics; Signal Transduction - physiology; Transforming Growth Factor alpha - physiology; Transforming Growth Factor beta - physiology; Up-Regulation - physiology; Wound Healing - genetics; Wound Healing - physiology; Human; Signal transduction; Motility; Gene; Dermatology; Primary; Genetics; Keratinocyte
• ISSN: 0022-202X; 1523-1747
• DOI: 10.1038/jid.2008.34

Regulation of human keratinocyte (HK) migration is critical for skin wound healing. Profiling HK migration-specific genes could help us gain a comprehensive understanding of the process. The main challenge is to separate genes that are unrelated to migration, but simultaneously induced by the same growth factor. In this study, we took advantage of a unique response of HKs to transforming growth factor-β (TGF-β), which inhibits proliferation but not migration of HKs, to suppress selectively the proliferation-related genes. Furthermore we stimulated HKs independently with TGF-α or insulin and identified the common genes and eliminated TGF-α- or insulin-specific genes. Under these conditions, we obtained profiles of the immediate-early genes (IEGs, at 30minutes), early genes (EGs, at 60minutes), and delayed-early genes (DEGs, at 120minutes) by microarray analyses, followed by quantitative real-time reverse transcription–PCR (QRT-PCR) validation and functional characterization by RNA interference (RNAi). Our results revealed the following: (1) 25 upregulated and 1 downregulated IEGs; (2) 58 upregulated and 15 downregulated EGs, and (3) 13 upregulated and 3 downregulated DEGs in both TGF-α- and insulin-stimulated HKs. Three genes, all encoding secreted molecules, were investigated in HK migration. These cell motility-specific gene profiles may prove useful to skin wound healing.