Morelli J G, Hake S S, Murphy R C, Norris D A
Department of Dermatology, University of Colorado School of Medicine, Denver 80262.
J Invest Dermatol. 1992 Jan;98(1):55-8. doi: 10.1111/1523-1747.ep12494602.
Leukotriene C4 (LTC4) is known to be a potent mitogen for cultured human neonatal melanocytes. We now demonstrate that leukotriene B4 (LTB4) can induce pigmentation in cultured human neonatal melanocytes in a dose-dependent fashion. The LTC4-induced mitogenesis is blocked by the cyclic nucleotide-dependent kinase inhibitor N-[2-(methyl-amino)ethyl]-5-isoquinolinesulfonamide dihydrochloride (H8). The LTB4-induced pigmentation is blocked by the protein kinase C inhibitor 1-(5-isoquinolinesulfonyl)-2-methylpiperazine dihydrochloride (H7). We propose that LTB4-induced pigmentation and LTC4-induced mitogenesis are important in vivo signals. Their different effects in our culture system are blocked by different protein kinase inhibitors.
白三烯C4(LTC4)已知是培养的人新生儿黑素细胞的一种强效促有丝分裂原。我们现在证明白三烯B4(LTB4)能够以剂量依赖性方式诱导培养的人新生儿黑素细胞色素沉着。LTC4诱导的有丝分裂作用被环核苷酸依赖性激酶抑制剂N-[2-(甲基氨基)乙基]-5-异喹啉磺酰胺二盐酸盐(H8)阻断。LTB4诱导的色素沉着被蛋白激酶C抑制剂1-(5-异喹啉磺酰基)-2-甲基哌嗪二盐酸盐(H7)阻断。我们提出,LTB4诱导的色素沉着和LTC4诱导的有丝分裂作用是重要的体内信号。它们在我们的培养系统中的不同作用被不同的蛋白激酶抑制剂阻断。