Department of Plastic Surgery, Rhode Island Hospital, Brown University School of Medicine, Providence, RI, USA.
Center for Disaster Medicine and Traumatology, Department of Clinical and Experimental Medicine, Linköping University Hospital, Linköping, Sweden.
Int Wound J. 2017 Dec;14(6):1006-1018. doi: 10.1111/iwj.12749. Epub 2017 Mar 29.
Connective tissue growth factor (CCN2/CTGF) and transforming growth factor β1 (TGF-β1) are important regulators of skin wound healing, but controversy remains regarding their expression in epithelial cell lineages. Here, we investigate the expression of CCN2 in keratinocytes during reepithelialisation and its regulation by TGF-β1. CCN2 was detected in the epidermis of healing full-thickness porcine wounds. Human keratinocytes were incubated with or without 10 ng/ml TGF-β1, and signalling pathways were blocked with 10-μM SIS3 or 20-μM PD98059. Semi-quantitative real-time PCR was used to study CCN2 mRNA expression, and western blot was used to measure CCN2, phosphorylated-ERK1/2, ERK1/2, phosphorylated-Smad3 and Smad2/3 proteins. CCN2 was transiently expressed in neoepidermis at the leading edge of the wound in vivo. In vitro, CCN2 expression was induced by TGF-β1 at 2 hours (7·5 ± 1·9-fold mRNA increase and 3·0 ± 0·6-fold protein increase) and 12 hours (5·4 ± 1·9-fold mRNA increase and 3·3 ± 0·6-fold protein increase). Compared with inhibiting the SMAD pathway, inhibiting the mitogen-activated protein kinase (MAPK) pathway was more effective in reducing TGF-β1-induced CCN2 mRNA and protein expression. Inhibition of the MAPK pathway had minimal impact on the activity of the SMAD pathway. CCN2 is expressed in keratinocytes in response to tissue injury or TGF-β1. In addition, TGF-β1 induces CCN2 expression in keratinocytes through the ras/MEK/ERK pathway. A complete understanding of CCN2 expression in keratinocytes is critical to developing novel therapies for wound healing and cutaneous malignancy.
结缔组织生长因子(CCN2/CTGF)和转化生长因子-β1(TGF-β1)是皮肤伤口愈合的重要调节因子,但它们在表皮细胞谱系中的表达仍存在争议。在这里,我们研究了 CCN2 在再上皮化过程中角质细胞中的表达及其受 TGF-β1 的调节。在愈合的全层猪伤口的表皮中检测到 CCN2。将人角质细胞与或不与 10ng/ml TGF-β1 孵育,并使用 10μM SIS3 或 20μM PD98059 阻断信号通路。使用半定量实时 PCR 研究 CCN2 mRNA 表达,并用 Western blot 测量 CCN2、磷酸化-ERK1/2、ERK1/2、磷酸化-Smad3 和 Smad2/3 蛋白。CCN2 在体内伤口前缘的新生表皮中短暂表达。在体外,TGF-β1 在 2 小时(mRNA 增加 7.5±1.9 倍,蛋白增加 3.0±0.6 倍)和 12 小时(mRNA 增加 5.4±1.9 倍,蛋白增加 3.3±0.6 倍)诱导 CCN2 表达。与抑制 SMAD 途径相比,抑制丝裂原活化蛋白激酶(MAPK)途径更有效地减少 TGF-β1 诱导的 CCN2 mRNA 和蛋白表达。抑制 MAPK 途径对 SMAD 途径的活性几乎没有影响。CCN2 在角质细胞中响应组织损伤或 TGF-β1 而表达。此外,TGF-β1 通过 ras/MEK/ERK 途径诱导角质细胞中 CCN2 的表达。全面了解角质细胞中 CCN2 的表达对于开发伤口愈合和皮肤恶性肿瘤的新疗法至关重要。