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组胺对黑素细胞增殖和白癜风角质形成细胞存活的影响。

Histamine effect on melanocyte proliferation and vitiliginous keratinocyte survival.

机构信息

Department of Dermatology, Dongguk University, Ilsan Hospital, Ilsandong-gu, Gyenggi-do, Korea.

出版信息

Exp Dermatol. 2010 Dec;19(12):1073-9. doi: 10.1111/j.1600-0625.2010.01133.x. Epub 2010 Nov 5.

Abstract

Repigmention of vitiligo requires melanocyte proliferation and migration. Keratinocytes have been shown to play a role in this process. Data from this laboratory showed that bee venom (BV) stimulated melanocyte proliferation and migration as well as melanogenesis. As histamine release is associated with BV, its effect on melanocyte proliferation and migration was examined. Cultured normal human melanocytes treated with histamine were studied with and without receptor-specific antagonists or agonists. The effect of histamine on vitiliginous keratinocytes, in cultured cells treated with a PI3K inhibitor in the presence of TNF-α, was also examined. Histamine exerted a more significant effect on melanocyte proliferation than on melanogenesis. This occurred through the H2 receptor with complex signalling to ERK, CREB, and Akt activation, which stimulated melanocyte migration. Histamine and the H2 receptor agonist also increased survival of vitiliginous, but not normal, keratinocytes, with NF-κB activation. Because expression levels of the H2 receptor was significantly decreased in depigmented compared to normally pigmented epidermis, in patients with vitiligo, histamine may increase the survival of vitiliginous keratinocytes. Overall, histamine stimulated the proliferation and migration of melanocytes and the vitiliginous keratinocyte survival, providing the basis for novel therapeutic approaches to vitiligo repigmentation.

摘要

白癜风的复色需要黑素细胞的增殖和迁移。已经表明角质形成细胞在这个过程中起作用。本实验室的数据表明,蜂毒 (BV) 刺激黑素细胞增殖、迁移和黑素生成。由于组胺释放与 BV 相关,因此研究了其对黑素细胞增殖和迁移的影响。用组胺处理培养的正常人黑素细胞,并使用受体特异性拮抗剂或激动剂进行研究。还研究了在存在 TNF-α 的情况下,PI3K 抑制剂处理的培养细胞中组胺对白癜风角质形成细胞的影响。与黑素生成相比,组胺对黑素细胞增殖的影响更显著。这是通过 H2 受体通过复杂的信号传导来实现的,ERK、CREB 和 Akt 的激活刺激了黑素细胞的迁移。组胺和 H2 受体激动剂也增加了白癜风但不是正常角质形成细胞的存活,NF-κB 被激活。由于与正常色素表皮相比,白癜风患者的表皮中 H2 受体的表达水平显著降低,因此组胺可能会增加白癜风角质形成细胞的存活。总的来说,组胺刺激黑素细胞的增殖和迁移以及白癜风角质形成细胞的存活,为白癜风复色的新治疗方法提供了基础。

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