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首页> 外文期刊>Annals of Dermatology >Protease-Activated Receptor-2 Is Associated with Terminal Differentiation of Epidermis and Eccrine Sweat Glands
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Protease-Activated Receptor-2 Is Associated with Terminal Differentiation of Epidermis and Eccrine Sweat Glands

机译:蛋白酶激活的受体2与表皮和内分泌汗腺的终末分化有关。

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Background Protease-activated receptor 2 (PAR-2) participates in various biological activities, including the regulation of epidermal barrier homeostasis, inflammation, pain perception, and melanosome transfer in the skin. Objective To evaluate the basic physiological role of PAR-2 in skin. Methods We investigated PAR-2 expression in human epidermis, skin tumors, and cultured epidermal cells using western blot and immunohistochemical analysis. Additionally, we examined the effect of the PAR-2 agonist, SLIGRL-NH2, on cultured keratinocytes. Results Strong PAR-2 immunoreactivity was observed in the granular layer of normal human skin and the acrosyringium of the eccrine sweat glands. In contrast, weak PAR-2 immunoreactivity was seen in the granular layer of callused skin and in the duct and gland cells of the eccrine sweat glands. Interestingly, PAR-2 immunoreactivity was very weak or absent in the tumor cells of squamous cell carcinoma (SCC) and syringoma. PAR-2 was detected in primary keratinocytes and SV-40T-transformed human epidermal keratinocytes (SV-HEKs), an immortalized keratinocyte cell line, but not in SCC12 cells. SV-HEKs that were fully differentiated following calcium treatment displayed higher PAR-2 expression than undifferentiated SV-HEKs. Treatment of cultured SV-HEKs with PAR-2 agonist increased loricrin and filaggrin expression, a terminal differentiation marker. Conclusion Our data suggest that PAR-2 is associated with terminal differentiation of epidermis and eccrine sweat glands.
机译:背景技术蛋白酶激活受体2(PAR-2)参与各种生物活动,包括调节表皮屏障稳态,炎症,疼痛感和皮肤中的黑素体转移。目的评估PAR-2在皮肤中的基本生理作用。方法我们使用免疫印迹和免疫组化分析技术研究了PAR-2在人表皮,皮肤肿瘤和培养的表皮细胞中的表达。此外,我们检查了PAR-2激动剂SLIGRL-NH2对培养的角质形成细胞的作用。结果在正常人皮肤的颗粒层和内分泌汗腺的顶动脉中都观察到了很强的PAR-2免疫反应性。相反,在老茧皮肤的颗粒层以及内分泌汗腺的导管和腺细胞中发现弱的PAR-2免疫反应性。有趣的是,在鳞状细胞癌(SCC)和脊髓空洞瘤的肿瘤细胞中,PAR-2免疫反应性非常弱或不存在。在原代角质形成细胞和SV-40T转化的人表皮角质形成细胞(SV-HEK)(一种永生化的角质形成细胞系)中检测到PAR-2,但在SCC12细胞中未检测到。钙处理后完全分化的SV-HEK比未分化的SV-HEK显示更高的PAR-2表达。用PAR-2激动剂处理培养的SV-HEKs会增加loricrin和丝聚蛋白的表达(终末分化标记)。结论我们的数据表明PAR-2与表皮和内分泌汗腺的终末分化有关。

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