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作 者:耿士玲[1] 单士军[1] 张同威[1] 吴剑[1] 王志华[1] 肖汀[1] 何春涤[1] 陈洪铎[1]
机构地区:[1]中国医科大学附属第一医院皮肤科,沈阳110001
出 处:《中华皮肤科杂志》2010年第3期181-183,共3页Chinese Journal of Dermatology
基 金:国家自狐科学基金(30400389);教育部高等学校博士学科点专项科研基金(20060159014),教育部创新团队基金(IRT0760),辽宁省创新团队基金(2008T192)
摘 要:目的探讨UVA对IFN-γ和TNF—α诱导的HaCaT细胞分泌和表达CXCL11/I—TAC的影响。方法用ELISA检测不同剂量UVA(2、4、8J/cm^2)照射后培养24h的HaCaT细胞上清中CXCL11/I-TAC分泌水平。用实时荧光定量PCR检测CXCLl1/I—TACmRNA表达水平。结果正常培养的HaCaT细胞仅分泌和表达微量的CXCL11/I—TAC蛋白或mRNA。当用10μg/L的IFN-γ和TNF—α联合刺激后,HaCaT细胞分泌或表达的CXCLI1/I-TAC显著升高。UVA在2、4、8J/cm^2呈剂量依赖性抑制CXCL11/I—TAC的分泌或表达。结论UVA照射抑制角质形成细胞分泌和表达CXCL11/I—TAC,从而在一定程度上降低了对Th1/Te1细胞的趋化。Objective To investigate the influences of UVA on the secretion and expression of chemokine CXCLll/I-TAC by HaCaT cells induced by interferon γ (IFN-γ) and tumor necrosis factor α (TNF-α). Methods HaCaT ceils were cultured in the presence of IFN-γ and TNF-α and irradiated with UVA of 2, 4 and 8 J/cm^2, respectively; those cells receiving neither treatment with IFN-γ or TNF-α nor UVA irradiation served as the negative control, and those receiving only cytokine treatment but no irradiation as the positive control. After another 24-hour culture, enzyme-linked immunosorbent assay (ELISA) was performed to detect the protein levels of CXCL11/I-TAC in the supernatant of HaCaT cells, real time PCR to measure the mRNA expression of CXCL11/I-TAC in these HaCaT cells. Results As far as the negative control HaCaT cells were concerned, there was a minor secretion of CXCL11/I-TAC protein and expression of CXCL1 I/I-TAC mRNA. After treatment with IFN-γ and TNF-α of 10 μg/L, the protein and mRNA expressions of CXCLI1/ I-TAC were synergistically upregulated, whereas the induced secretion and expression of CXCL11/I-TAC by HaCaT cells were dose-dependently inhibited by UVA irradiation. Conclusions UVA irradiation inhibits the secretion and expression of CXCL11/I-TAC by HaCaT cells, which in turn suppresses the chemotaxis of Th1/ Tc 1 ceils in some degree.
分 类 号:R751[医药卫生—皮肤病学与性病学]
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