Rollins B J, Pober J S
Division of Medicine, Dana-Farber Cancer Institute, Boston, MA 02115.
Am J Pathol. 1991 Jun;138(6):1315-9.
The authors have demonstrated that human interleukin-4 (IL-4) induces increased expression of the mRNA encoding the monocyte-specific chemoattractant and activator, MCP-1/JE, in human endothelial cells (EC). In addition, treatment of ECs with IL-4 resulted in the synthesis and secretion of MCP-1/JE protein. While IL-4 did not significantly influence the induced expression of MCP-1/JE mRNA by interleukin-1 (IL-1) or tumor necrosis factor, concomitant treatment with IL-4 and IL-1 caused more secretion of MCP-1/JE protein than either cytokine alone. These results suggest that EC-produced MCP-1/JE may mediate some of IL-4's effects on monocyte physiology in vivo, including IL-4's anti-tumor properties.
作者已证明,人白细胞介素-4(IL-4)可诱导人内皮细胞(EC)中编码单核细胞特异性趋化因子和激活剂MCP-1/JE的mRNA表达增加。此外,用IL-4处理内皮细胞会导致MCP-1/JE蛋白的合成与分泌。虽然IL-4对白细胞介素-1(IL-1)或肿瘤坏死因子诱导的MCP-1/JE mRNA表达没有显著影响,但IL-4与IL-1联合处理比单独使用任何一种细胞因子都会导致更多的MCP-1/JE蛋白分泌。这些结果表明,内皮细胞产生的MCP-1/JE可能介导了IL-4在体内对单核细胞生理的某些影响,包括IL-4的抗肿瘤特性。