Kim Peter K M, Weller Richard, Hua Yun, Billiar Timothy R
Department of Surgery, University of Pittsburgh Medical Center, NW607 MUH, Pittsburgh, PA 15213, USA.
Biochem Biophys Res Commun. 2003 Mar 7;302(2):290-5. doi: 10.1016/s0006-291x(03)00186-4.
Ultraviolet irradiation (UV) can induce keratinocyte apoptosis by activating death receptors that recruit the intracellular adaptor molecule FADD/MORT1 (Fas-associating death domain protein/mediator of receptor-induced toxicity). We hypothesized that UV could alter FADD expression levels to augment UV-induced keratinocyte apoptosis. In a dose-dependent manner UV B irradiation increased the expression of FADD protein in a human keratinocyte cell line (CCD-1106) with a corresponding increase in caspase-8 cleavage and cellular apoptosis. FADD overexpression induced cell death in 80% of cells compared with 10% spontaneous cell death in controls. Inhibition of FADD protein by adenoviral expression of anti-sense FADD reduced keratinocyte apoptosis. Regulation of FADD expression by UV may serve to enhance death receptor-mediated keratinocyte death.
紫外线照射(UV)可通过激活死亡受体诱导角质形成细胞凋亡,这些死亡受体招募细胞内衔接分子FADD/MORT1(Fas相关死亡结构域蛋白/受体诱导毒性的介质)。我们推测紫外线可能改变FADD表达水平,以增强紫外线诱导的角质形成细胞凋亡。紫外线B照射以剂量依赖方式增加人角质形成细胞系(CCD-1106)中FADD蛋白的表达,同时半胱天冬酶-8裂解和细胞凋亡相应增加。与对照中10%的自发细胞死亡相比,FADD过表达诱导80%的细胞死亡。通过腺病毒表达反义FADD抑制FADD蛋白可减少角质形成细胞凋亡。紫外线对FADD表达的调节可能有助于增强死亡受体介导的角质形成细胞死亡。