Tanaka T, Danno K, Ikai K, Imamura S
Department of Dermatology, Faculty of Medicine, Kyoto University, Japan.
J Invest Dermatol. 1988 Mar;90(3):399-401. doi: 10.1111/1523-1747.ep12456487.
The effects of substance P and substance K, which are coexpressed in the same mRNA as a beta-preprotachykinin in peripheral tissues and released in the inflammatory lesion of the skin, were examined on epidermal proliferation using spontaneously transformed mouse epidermal cell line (Pam 212 cells). Substance P stimulated the synthesis of DNA of Pam 212 cells in the medium containing 2%-10% fetal calf serum (FCS). Stimulation of DNA synthesis was dose dependent if the cells were cultured in the medium containing 2% FCS (quiescent condition). This effect was inhibited by spantide. In a serum-free medium, substance P had no effect on keratinocyte proliferation. In contrast, substance K, which shares a common amino acid sequence with substance P on its C-terminal, did not affect DNA synthesis of Pam 212 cells in either medium condition. Substance P released in inflammation may stimulate epidermal proliferation.
P物质和K物质与β-前速激肽原在同一信使核糖核酸中共同表达于外周组织,并在皮肤炎症损伤部位释放。本研究使用自发转化的小鼠表皮细胞系(Pam 212细胞)检测了P物质和K物质对表皮增殖的影响。P物质在含有2%-10%胎牛血清(FCS)的培养基中刺激Pam 212细胞的DNA合成。如果细胞在含有2% FCS的培养基中培养(静止状态),DNA合成的刺激呈剂量依赖性。这种作用可被spantide抑制。在无血清培养基中,P物质对角质形成细胞增殖无影响。相比之下,K物质在其C末端与P物质具有共同的氨基酸序列,在两种培养基条件下均不影响Pam 212细胞的DNA合成。炎症中释放的P物质可能刺激表皮增殖。