Department of Biologia e Chimica Agro-Forestale ed Ambientale, University of Bari, 70126 Bari, Italy.
Peptides. 2011 Sep;32(9):1815-24. doi: 10.1016/j.peptides.2011.07.004. Epub 2011 Jul 14.
This work showed the effect of pheromone plantaricin A (PlnA) on the proliferation and migration of the human keratinocytes NCTC 2544. PlnA was chemically synthesized and used as pure peptide or biologically synthesized during co-cultivation of Lactobacillus plantarum DC400 and Lactobacillus sanfranciscensis DPPMA174. The cell-free supernatant (CFS) was used as the crude preparation containing PlnA. The inductive effect of PlnA on the proliferation of NCTC 2544 cells was higher than that found for hyaluronic acid, a well known skin protective compound. As shown by scratch assay and image analyses, PlnA enhanced the migration of NCTC 2544 cells. Compared to the basal serum free medium (control), the highest inductive effect was found using 10μg/ml of chemically synthesized PlnA. Similar results (P>0.05) were found for CFS. In agreement, the percentage of the starting scratch area was decreased after treatment (24h) with PlnA. The expression of transforming growth factor-β1 (TGF-β1), keratinocyte growth factor 7 (FGF7), vascular endothelial growth factor (VEGF-A), and interleukin-8 (IL-8) genes was affected by PlnA. Compared to control, TGF-β1 gene was under expressed in the first 4h of treatments and up-regulated after 8-24h. On the contrary, FGF7 gene was strongly up-regulated in the first 4h of treatments. Compared to control, VEGF-A and IL-8 genes were always up-regulated during the 4-24h from scratching. Since capable of promoting the proliferation and migration of the human keratinocytes and of stimulating IL-8 cytokine, the use of PlnA for dermatological purposes should be considered.
这项工作研究了信息素植物素 A(PlnA)对人角质形成细胞 NCTC 2544 增殖和迁移的影响。PlnA 经化学合成,并在植物乳杆菌 DC400 和旧金山乳杆菌 DPPMA174 共培养时生物合成,细胞培养液上清(CFS)用作含有 PlnA 的粗制剂。PlnA 对 NCTC 2544 细胞增殖的诱导作用高于透明质酸(一种众所周知的皮肤保护化合物)。划痕实验和图像分析表明,PlnA 增强了 NCTC 2544 细胞的迁移。与基础无血清培养基(对照)相比,使用 10μg/ml 化学合成 PlnA 时诱导作用最高。CFS 也有类似的结果(P>0.05)。结果一致,在用 PlnA 处理(24 小时)后,起始划痕面积的百分比降低。转化生长因子-β1(TGF-β1)、角质形成细胞生长因子 7(FGF7)、血管内皮生长因子(VEGF-A)和白细胞介素-8(IL-8)基因的表达受 PlnA 影响。与对照相比,TGF-β1 基因在处理的前 4 小时表达下调,8-24 小时后上调。相反,FGF7 基因在处理的前 4 小时内强烈上调。与对照相比,VEGF-A 和 IL-8 基因在划痕后 4-24 小时内始终上调。由于 PlnA 能够促进人角质形成细胞的增殖和迁移,并刺激白细胞介素-8 细胞因子的产生,因此应考虑将其用于皮肤病学用途。