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Increased caspase-3 and altered expression of apoptosis-associated proteins, Bcl-2 and Bax in lichen planus.

机译:扁平苔藓中caspase-3的增加和凋亡相关蛋白Bcl-2和Bax表达的改变。

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BACKGROUND: Lichen planus (LP) is a chronic inflammatory disease of probable immune-based aetiology. The pathogenesis of LP is unclear, but apoptotic changes in epidermal (epithelial) cells have been reported. OBJECTIVE: To evaluate apoptosis in LP through studying caspase-3 expression and to determine whether the apoptosis-associated proteins Bcl-2 and Bax are significantly involved in the pathogenesis of LP. METHODS: In total, 25 lesional biopsy specimens [15 cutaneous LP (CLP) and 10 oral LP (OLP)] and 10 control specimens [5 normal skin and 5 normal oral mucosa] were studied using immunochemical methods for the expression of caspase-3, Bcl-2 and Bax proteins. RESULTS: Compared with controls, a significant increase in caspase-3 and Bax protein expressions were found in LP lesions. Basal cell expression of caspase-3 was positive in 14 cases (56%), and 12 cases (48%) showed mild expression. Caspase-3 expression in inflammatory infiltrate was positive in 13 cases (52%). Of these, 12 cases (48%) showed mild positivity. Bax was localized mostly to the upper prickle layer. Basal cell expression of Bcl-2 was negative in 18 (72%) cases, with no significant difference between patients with LP and controls. Bcl-2 was expressed in the inflammatory infiltrate in 15 cases of LP (60%), showing mild expression in 12 cases (48%). Compared with CLP, there was a significant increase in caspase-3 expression in OLP, despite the nonsignificant difference in Bcl-2 and Bax protein expressions by the epithelial cells. CONCLUSION: Increased caspase-3 and altered expression of Bcl-2 and Bax were found in LP, indicating the possible involvement of these proteins in the pathogenesis of the disease. The observed increase in apoptosis in OLP compared with CLP might explain the difference in clinical behaviour that distinguishes these LP variants.
机译:背景:扁平苔藓(LP)是一种可能的基于免疫的病因的慢性炎症性疾病。 LP的发病机理尚不清楚,但是已经报道了表皮(上皮)细胞的凋亡变化。目的:通过研究caspase-3的表达来评估LP的凋亡,并确定凋亡相关蛋白Bcl-2和Bax是否与LP的发病机制密切相关。方法:采用免疫化学方法研究了25个病灶活检标本[15个皮肤LP(CLP)和10个口服LP(OLP)]和10个对照标本[5个正常皮肤和5个正常口腔黏膜]表达caspase-3的表达。 ,Bcl-2和Bax蛋白。结果:与对照组相比,LP病变中caspase-3和Bax蛋白表达显着增加。 caspase-3的基础细胞表达阳性14例(56%),轻度表达12例(48%)。炎性浸润中Caspase-3表达阳性13例(52%)。其中12例(48%)呈轻度阳性。 Bax主要定位在上刺皮层。 Bcl-2的基底细胞表达在18例(72%)病例中为阴性,LP患者和对照组之间无显着差异。 Bcl-2在15例LP的炎症浸润中表达(60%),在12例(48%)中显示轻度表达。与CLP相比,尽管上皮细胞的Bcl-2和Bax蛋白表达没有显着差异,但OLP中caspase-3的表达显着增加。结论:LP中发现caspase-3增加,Bcl-2和Bax表达改变,提示这些蛋白可能参与了疾病的发病。与CLP相比,观察到的OLP细胞凋亡增加可能解释了区分这些LP变体的临床行为差异。

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