摘要
目的:探讨转化生长因子β1(TGF-β1)、肿瘤坏死因子(TNF)和维拉帕米对严重烧伤小鼠早期腹腔巨噬细胞(Mφ)CD14表达的影响。方法:BALB/c小鼠被随机地分成烧伤组和假烫组,将收集到的腹腔巨噬细胞分别加入不同浓度TGF-β1(0.02,0.20,2.00μg/ml)、TNF(0.1,1.0,10.0μg/ml)和维拉帕米(10,100,1000pmol/ml)培养。用细胞原位杂交方法,观察TGF-β1、TNF和维拉帕米对小鼠MφCD14mRNA表达的影响。结果:(1)烧伤后腹腔MφCD14mRNA的表达明显增加。(2)0.02,0.20μg/mlTGF-β1可使烧伤小鼠MφCD14mRNA表达增加,2μg/ml则可使烧伤小鼠MφCD14mRNA表达减少。TNF、维拉帕米各浓度对烧伤小鼠MφCD14mRNA表达均无明显影响。结论:TGF-β1能通过改变MφCD14mRNA的表达,调节其功能状态。TNF。
Objective: To study the effects of TGF-β_1,TNF and verapamil on CD14 mRNA in peritoneal macrophages in severely burned mice in order to provide an experimental evidence for its further studies. Methods: Mouse were randomly divided into burn group and sham group. Mice peritoneal macrophages from burn group (n=5) or sham group (n=5) were isolated and incubated with TGF-β_1 (0.02,0.20,2.00 μg/ml), TNF(0.1,1.0,10.0 μg/ml) and verapamil(10,100,1000 pm/ml). The peritoneal macrophage CD14 mRNA expression was observed by in situ hybridization analysis. Results: (1) Significantly increased CD14 mRNA staining granules in cytoplasm were found in burn mice. (2) TGF-β_1 (0.02,0.20 μg/ml) enhanced the expression of CD14 in burned mice macrophages, and these effects could be reversed when the cells were treated with the highest dose. No difference was observed between macrophages from burned mice treated with TNF and verapamil and from burned mice untreated. Conclusion: TGF-β_1 can significantly change macrophage sensitivity possibly because of the changes of CD14 mRNA expression. These effects do not occur in burn mice incubated with TNF and verapamil.
出处
《第二军医大学学报》
CAS
CSCD
北大核心
1998年第S1期107-109,共3页
Academic Journal of Second Military Medical University