Baroni A, Buommino E, Paoletti I, Orlando M, Ruocco E, Ruocco V
Clinica Dermatologica, Facoltà di Medicina e Chirurgia II, Università degli Studi di Napoli, 80131 Naples, Italy.
Br J Dermatol. 2004 Jun;150(6):1070-80. doi: 10.1111/j.1365-2133.2004.05919.x.
Captopril is an angiotensin-converting enzyme inhibitor with sulphydryl groups in its chemical structure. It is commonly used as an antihypertensive drug. The occurrence of pemphigus vulgaris has repeatedly been reported in patients receiving captopril. The capacity of captopril and pemphigus serum to induce acantholysis, in vivo or in vitro, has been demonstrated experimentally.
To show that captopril and pemphigus serum, acting by a biochemical and immunological mechanism, respectively, trigger apoptosis.
Human keratinocyte cells were treated with 15 mmol L-1 captopril or with pemphigus serum. DNA was extracted and the terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end labelling method was used to detect apoptosis.
DNA fragmentation occurred after 72 h of treatment. Increased expression of p53, c-myc and inducible nitric oxide (NO) synthase (iNOS) mRNA were observed by polymerase chain reaction (PCR) in the treated cells compared with the untreated ones. The increase in iNOS gene expression was associated with overproduction of NO. Moreover, the addition of 1 mmol L-1N-monomethyl-L-arginine, a structural analogue of arginine, reduced nitrite levels by about 70% in cells treated with captopril or pemphigus serum. Western blot analysis revealed an overexpression of heat shock protein 70 (hsp70) in cells treated with captopril or pemphigus serum. Finally, total inhibition of the keratinocyte transglutaminase gene was shown by PCR analysis in the same samples, compared with control cells.
These data demonstrate the involvement of apoptosis in keratinocytes treated with captopril or pemphigus serum, with induction of the iNOS gene and hsp70 in the cascade of events leading to programmed cell death.
卡托普利是一种化学结构中含有巯基的血管紧张素转换酶抑制剂,常用作抗高血压药物。接受卡托普利治疗的患者中反复出现寻常型天疱疮的病例。实验已证明卡托普利和天疱疮血清在体内或体外具有诱导棘层松解的能力。
证明卡托普利和天疱疮血清分别通过生化和免疫机制引发细胞凋亡。
用人角质形成细胞分别用15 mmol/L卡托普利或天疱疮血清处理。提取DNA,采用末端脱氧核苷酸转移酶介导的脱氧尿苷三磷酸缺口末端标记法检测细胞凋亡。
处理72小时后出现DNA片段化。与未处理的细胞相比,经聚合酶链反应(PCR)检测,处理后的细胞中p53、c-myc和诱导型一氧化氮(NO)合酶(iNOS)mRNA表达增加。iNOS基因表达的增加与NO的过量产生有关。此外,添加1 mmol/L的精氨酸结构类似物N-单甲基-L-精氨酸可使卡托普利或天疱疮血清处理的细胞中亚硝酸盐水平降低约70%。蛋白质印迹分析显示,用卡托普利或天疱疮血清处理的细胞中热休克蛋白70(hsp70)表达上调。最后,与对照细胞相比,PCR分析显示相同样品中角质形成细胞转谷氨酰胺酶基因完全被抑制。
这些数据表明,在用卡托普利或天疱疮血清处理的角质形成细胞中,细胞凋亡参与其中,在导致程序性细胞死亡的一系列事件中诱导了iNOS基因和hsp70。