Grando S A, Horton R M, Mauro T M, Kist D A, Lee T X, Dahl M V
Department of Dermatology of University of Minnesota, Minneapolis, USA.
J Invest Dermatol. 1996 Sep;107(3):412-8. doi: 10.1111/1523-1747.ep12363399.
Human epidermal keratinocytes synthesize, secrete, and degrade acetylcholine and use their cell-surface nicotinic and muscarinic cholinergic receptors to mediate the autocrine and paracrine effects of acetyl-choline. Because acetylcholine modulates transmembrane Ca2+ transport and intracellular metabolism in several types of cells, we hypothesized that cholinergic agents might have similar effects on keratinocytes. Nicotine increased in a concentration-dependent manner the amount of 45Ca2+ taken up by keratinocytes isolated from human neonatal fore-skins. This effect was abolished in the presence of the specific nicotinic antagonist mecamylamine, indicating that it was mediated by keratinocyte nicotinic acetylcholine receptor(s). The sequences encoding the alpha 5 and alpha 7 nicotinic receptor subunits were amplified from cDNA isolated from cultured keratinocytes. These subunits, as well as the alpha 3, beta 2, and beta 4 subunits previously found in keratinocytes, can be components of Ca(2+)-permeable nicotinic receptor channels. To learn how activation of keratinocyte nicotinic receptors affected the rate of cell differentiation, we measured the nicotinic cholinergic effects on the expression of differentiation markers by cultured keratinocytes. Long-term incubations with micromolar concentrations of nicotine markedly increased the number of cells forming cornified envelopes and the number of cells staining with antibodies to suprabasal keratin 10, transglutaminase type I, involucrin, and filaggrin. The increased production of these differentiation-associated proteins was verified by Western blotting. Because nicotinic cholinergic stimulation causes transmembrane Ca2+ transport into keratinocytes, and because changes in concentrations of intracellular Ca2+ are known to alter various keratinocyte functions, including differentiation, the subcellular mechanisms mediating the autocrine and paracrine actions of epidermal acetylcholine on keratinocytes may involve Ca2+ as a second messenger.
人表皮角质形成细胞能合成、分泌并降解乙酰胆碱,且利用其细胞表面的烟碱型和毒蕈碱型胆碱能受体来介导乙酰胆碱的自分泌和旁分泌作用。由于乙酰胆碱可调节多种细胞类型中的跨膜Ca2+转运及细胞内代谢,我们推测胆碱能药物可能对角质形成细胞有类似作用。尼古丁以浓度依赖性方式增加了从人新生儿包皮分离出的角质形成细胞摄取的45Ca2+量。在特异性烟碱拮抗剂美加明存在的情况下,这种作用被消除,表明它是由角质形成细胞的烟碱型乙酰胆碱受体介导的。从培养的角质形成细胞分离的cDNA中扩增出编码α5和α7烟碱受体亚基的序列。这些亚基,以及先前在角质形成细胞中发现的α3、β2和β4亚基,可能是Ca(2+)通透烟碱受体通道的组成部分。为了了解角质形成细胞烟碱受体的激活如何影响细胞分化速率,我们测量了烟碱型胆碱能对培养的角质形成细胞分化标志物表达的影响。用微摩尔浓度的尼古丁进行长期孵育,显著增加了形成角质包膜的细胞数量以及用抗基底上层角蛋白10、I型转谷氨酰胺酶、内披蛋白和丝聚蛋白抗体染色的细胞数量。通过蛋白质印迹法证实了这些与分化相关蛋白质的产量增加。由于烟碱型胆碱能刺激导致跨膜Ca2+转运进入角质形成细胞,并且由于已知细胞内Ca2+浓度的变化会改变包括分化在内的各种角质形成细胞功能,因此介导表皮乙酰胆碱对角质形成细胞自分泌和旁分泌作用的亚细胞机制可能涉及Ca2+作为第二信使。