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蛋白激酶Cδ在X射线诱导的角质形成细胞凋亡中的作用。

Role of protein kinase C delta in X-ray-induced apoptosis of keratinocyte.

作者信息

Lee Young-Sook, Sohn Kyung-Cheol, Kim Ki-Hwan, Cho Moon-June, Hur Gang Min, Yoon Tae-Jin, Kim Sung Kyu, Lee Kyungmoon, Lee Jeung-Hoon, Kim Chang Deok

机构信息

Department of Dermatology and Research Institute for Medical Sciences, School of Medicine, Chungnam National University, Daejeon, Korea.

出版信息

Exp Dermatol. 2009 Jan;18(1):50-6. doi: 10.1111/j.1600-0625.2008.00761.x. Epub 2008 Jul 7.

Abstract

In this study, we investigated the process of X-ray-induced apoptosis of skin keratinocyte, and the functional role of protein kinase C delta (PKCdelta) and downstream signalling cascade. High-dose X-ray irradiation (10 Gy) led to the apoptosis of HaCaT keratinocyte, accompanied by PKCdelta cleavage. Treatment with PKCdelta inhibitor and adenoviral transduction of dominant-negative PKCdelta clearly inhibited the X-ray-induced apoptosis of keratinocyte. In addition, X-ray induced the phosphorylation of extracellular signal-regulated kinases 1/2 (ERK1/2) and inhibition by ERK1/2 inhibitor abrogated the X-ray-induced apoptosis. Interestingly, overexpression of dominant-negative PKCdelta markedly blocked the X-ray-induced phosphorylation of ERK1/2, suggesting that ERK1/2 is the functional downstream effector of PKCdelta. Next, we investigated the difference between UVB and X-ray response. UVB induced the apoptosis of keratinocyte in a PKCdelta-dependent manner, similar to X-ray response. However, UVB irradiation induced the phosphorylation of c-jun N-terminal kinases (JNK) and inhibition of JNK significantly protected the UVB-induced apoptosis. These results demonstrate that PKCdelta is a key regulator in X-ray-induced apoptosis of keratinocyte and suggest that there is subtle difference in downstream signalling cascade between UVB and X-ray response of keratinocyte.

摘要

在本研究中,我们调查了X射线诱导皮肤角质形成细胞凋亡的过程,以及蛋白激酶Cδ(PKCδ)和下游信号级联反应的功能作用。高剂量X射线照射(10 Gy)导致HaCaT角质形成细胞凋亡,并伴有PKCδ的裂解。用PKCδ抑制剂处理以及通过腺病毒转导显性负性PKCδ可明显抑制X射线诱导的角质形成细胞凋亡。此外,X射线诱导细胞外信号调节激酶1/2(ERK1/2)磷酸化,而ERK1/2抑制剂的抑制作用可消除X射线诱导的凋亡。有趣的是,显性负性PKCδ的过表达显著阻断了X射线诱导的ERK1/2磷酸化,表明ERK1/2是PKCδ的功能性下游效应分子。接下来,我们研究了紫外线B(UVB)和X射线反应之间的差异。UVB以PKCδ依赖的方式诱导角质形成细胞凋亡,与X射线反应相似。然而,UVB照射诱导c-jun氨基末端激酶(JNK)磷酸化,抑制JNK可显著保护UVB诱导的凋亡。这些结果表明,PKCδ是X射线诱导角质形成细胞凋亡的关键调节因子,并提示角质形成细胞UVB和X射线反应的下游信号级联反应存在细微差异。

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