Department of Pathology & Laboratory Medicine, Indiana University School of Medicine, 1120 South Drive, Fesler Hall 403, Indianapolis, IN 46202, USA.
Prostaglandins Leukot Essent Fatty Acids. 2009 Oct;81(4):279-90. doi: 10.1016/j.plefa.2009.05.025. Epub 2009 Jul 22.
We have previously demonstrated that the EP1 subtype of PGE2 receptor is expressed in the differentiated compartment of normal human epidermis and is coupled to intracellular calcium mobilization. We therefore hypothesized that the EP1 receptor is coupled to keratinocyte differentiation. In in vitro studies, radioligand binding, RT-PCR, immunoblot and receptor agonist-induced second messenger studies demonstrate that the EP1 receptor is up-regulated by high cell density in human keratinocytes and this up-regulation precedes corneocyte formation. Moreover, two different EP1 receptor antagonists, SC51322 and AH6809, both inhibited corneocyte formation. SC51322 also inhibited the induction of differentiation-specific proteins, cytokeratin K10 and epidermal transglutaminase. We next examined the immunolocalization of the EP1 receptor in non-melanoma skin cancer in humans. Well-differentiated SCCs exhibited significantly greater membrane staining, while spindle cell carcinomas and BCCs had significantly decreased membrane staining compared with normal epidermis. This data supports a role for the EP1 receptor in regulating keratinocyte differentiation.
我们之前已经证明,前列腺素 E2 受体的 EP1 亚型在正常人体表皮的分化区表达,并与细胞内钙动员偶联。因此,我们假设 EP1 受体与角质形成细胞分化偶联。在体外研究中,放射性配体结合、RT-PCR、免疫印迹和受体激动剂诱导的第二信使研究表明,EP1 受体在人角质形成细胞中通过高细胞密度而上调,这种上调发生在角质形成细胞形成之前。此外,两种不同的 EP1 受体拮抗剂 SC51322 和 AH6809 均抑制角质形成细胞的形成。SC51322 还抑制了角蛋白 K10 和表皮转谷氨酰胺酶等分化特异性蛋白的诱导。接下来,我们检查了人类非黑色素瘤皮肤癌中 EP1 受体的免疫定位。高分化 SCC 表现出明显增加的膜染色,而梭形细胞癌和基底细胞癌与正常表皮相比,膜染色明显减少。这些数据支持 EP1 受体在调节角质形成细胞分化中的作用。