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作 者:周燕斌[1] 叶任高[1] 李幼姬[1] 谢灿茂[1] 胡斌[2]
机构地区:[1]广州中山大学附属第一医院内科,广州510080 [2]广州中山大学达安基因中心,广州510080
出 处:《免疫学杂志》2006年第2期165-167,171,共4页Immunological Journal
摘 要:目的探讨中药狼疮方对狼疮样BXSB小鼠肺组织CD134/CD134L和RANTES表达的影响。方法采用BXSB小鼠模型,随机分为3组:狼疮方治疗组、强的松治疗组、未治疗组,每组6只,疗程10周。另设与BXSB小鼠同基因的正常C57BL/6小鼠6只为正常对照组。分别取小鼠肺组织,应用逆转录-荧光定量-聚合酶链反应(RT-FQ-PCR)技术定量测定小鼠肺组织CD134、CD134L和趋化因子RANTES的mRNA表达水平。结果①未治疗组小鼠肺组织CD134、CD134L mRNA和RANTESmRNA的表达水平都显著高于正常对照组(P<0.01,P<0.05);经强的松或中药狼疮方治疗后,BXSB小鼠肺组织CD134、CD134L及RANTES的mRNA表达都受到明显抑制,显著低于未治疗组(P<0.01,P<0.05);且接近正常水平,与正常对照组无显著性差异(P>0.05)。②BXSB小鼠肺组织RANTES的mRNA表达水平与CD134L的mRNA表达水平呈显著的正相关关系(r=0.793,P<0.05),而与CD134的mRNA表达水平无显著的相关关系(r=0.412,P>0.05)。结论中药狼疮方具有与强的松类似的免疫抑制作用,可显著抑制狼疮样小鼠肺组织CD134/CD134L共刺激信号表达;并下调肺组织RANTES mRNA表达水平,具有一定的肺脏保护作用。Objective To investigate the effects of lupus recipe on gene expressions of CD134, CD134L, and RANTES in lung cells of lupus-prone BXSB mice. Methods Eighteen male lupus-prune BXSB mice models were divided into three groups: untreated group, lupus recipe (LR) treated group,and prednisone treated group. All mice were sacrificed in 10 weeks. Control group was set up which consisted of 6 normal syngeneic C57BL/6 male mice. The mRNA expressions of CD134, CD134L, and RANTES in lung cells were detected by RT-FQ-PCR. Results ① The mRNA expressions of CD134, CD134L, and RANTES in lung cells of untreated group were obviously higher than those of control groups (P 〈 0.05, P 〈 0.01). The LR or prednisone reduced significantly the CD134, CD134L, and RANTES mRNA expressions (P 〈 0.05, P 〈 0.01, comparing with untreated group), while the difference between the treated group and the control group wns not significant. ② There was a positive correlation between CD134L mRNA expression and RANTES mRNA expression in lung cells of model mice (r = 0.793, P 〈 0.05). Conclusion The abnormal expressions of CD134, CD134L mRNA are well evidenced in the lungoflupus-prone BXSB mice. Strong expression of RANTES mRNA is likely mediated by CD134/CD134L signal pathway. LR and corticusteroide could obviously inhibit the mRNA expressions of CD134, CD134L, and RANTES.
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