机构地区:[1]山西省人民医院普外科,太原030012 [2]河北省邢台市人民医院肿瘤外科
出 处:《中华实验外科杂志》2011年第10期1686-1689,共4页Chinese Journal of Experimental Surgery
基 金:山西省自然科学基金资助项目(2009011052-2)
摘 要:目的观察不同浓度γ干扰素(IFN-γ)作用下大鼠脾脏来源的树突状细胞(Dc)中吲哚胺2,3-双加氧酶(IDO)mRNA和蛋白表达的变化及IDO对同种异体T淋巴细胞增殖的影响。方法应用细胞因子体外诱导培养大鼠脾脏来源DC,应用流式细胞仪测定大鼠DC特异性分子OX62和表面分子CD80、CD86的表达。分别用不同浓度(0、100、300、500U/m1)的IFN-γ诱导作用DC后,实时聚合酶链反应(Real-timePCR)测定DC中IDOmRNA的相对表达水平,Westernblot检测DC中IDO蛋白在Dc中的表达水平。同种异体混合淋巴细胞反应(MLR)检测不同浓度IFN-γ诱导后的DC对同种异体T淋巴细胞增殖的影响。结果体外诱导培养的DC光学娩微镜下观察,具有典型的树枝状突起。OX62表达率达到80%以上,CD80、CD86的阳性表达也在80%左右;DC的IDOmRNA(2-ΔΔCt值分别为:1.010±0.094、1.340±0.114、1.700±0.087、2.080±0.150)和蛋白的相对表达量(分别为-0.861±0.612、1.155±0.059、1.308±0.068、1.755±0.118)随着IFN.7作用浓度的增大逐渐增大,分别为:不同浓度组间差异有统计学意义(P〈0.05);各组IFN-γ作用后DC与对照组比较,T淋巴细胞的增殖率显著降低(P〈0.05);且随着IFN-γ作用浓度的增大T淋巴细胞的增殖率逐渐降低,A值分别为:0.458±0.041、0.423±0.030、0.349±0.019、0.312±0.036,各组间差异有统计学意义(P〈0.05)。结论采用改良的培养黏附法体外获得纯度较高的大鼠脾脏来源的DC;IFN-γ可以诱导大鼠脾脏来源DC表面活性IDO的表达增加,减弱脾脏DC对同种T细胞增殖的刺激能力.Objective To investigate the expression chenges of indoleamine 2,3-dioxygenase (IDO) mRNA and protein in dendritic cells (DCs) derived from rat spleen in vitro as well as the effect of IDO on proliferation of allogeneic T lymphocytes in terms of different concentrations of interferon (IFN)-γ. Methods We first extracted DCs from the spleen of rats, then measured the expression of DC-speeific molecules and surface molecules CDSO and CD86 in rats by flow cytometry. DCs were induced by IFN-γ at differenct concentrations (0, 100, 300, 500 U/ml). Real-time polymerase chain reactio (PCR) and Western blotting were used to detect the relative expression levels of IDO mRNA and protein in DCs. Allo- geneic mixed lymphocyte reaction (MLR) was applied to test the effect of DCs induced with different concentrations of IFN-γ on allogeneic T lymphocyte proliferation. Results The results showed that the spleenderived DCs from rats cultured for 10 days had a typical dendritic morphology, whose expression rate of OX62 was above 80% and positive expression rate of CDS0 and CD96 was more than 75% and 90% respectively. The expression levels of IDO mRNA ( 1. 010 ±0. 094, 1. 340 ±0. 114, 1. 700 ±0. 087, 2. 080 ±0. 150) and protein (0. 861 ±0. 612, 1. 155 ±0. 059, 1. 308 ±0. 068, 1. 755 ±0. 118) were increased gradually with the increase of concentrations of IFN-γ, which showed significant difference between any two groups. As compared with the control group, the groups induced by the IFN-γ had a decrease in T lympho- cyte proliferation of DCs (P 〈 0. 05). Besides, with the increased concentration of IFN-γ, the rate of T lymphocyte proliferation was decreased gradually and there was significant difference between ant two groups (P 〈 0. 05 ). Conclusion The IFN-γ can induce the increased expression of IDO in spleen-derived DCs from rats, and the decreased stimulation capacity of spleen DCs to the antigen-specific T cell response.
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