首页> 外文期刊>The journal of immunology >Two Loci on Chromosome 15 Control Experimentally Induced Arthritis through the Differential Regulation of IL-6 and Lymphocyte Proliferation
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Two Loci on Chromosome 15 Control Experimentally Induced Arthritis through the Differential Regulation of IL-6 and Lymphocyte Proliferation

机译:通过IL-6和淋巴细胞增殖的差异调节,在15号染色体上控制实验诱导的关节炎的两个基因座。

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Using genetic linkage analysis of proteoglycan-induced arthritis (PGIA), a murine model for rheumatoid arthritis, we identified two loci, Pgia8 and Pgia9 , on chromosome 15 (chr15) that appear to be implicated in disease susceptibility. Immunization of congenic strains carrying the entire chr15 and separately each of the two loci of DBA/2 arthritis-resistant origin in susceptible BALB/c background confirmed locations of two loci on chr15: the major Pgia9 and lesser Pgia8 locus. Distal part of chr15 ( Pgia9 ) showed a major suppressive effect on PGIA susceptibility in females (40%, p 0.001), whereas the effect of this locus in congenic males was still significant but weaker. Proximal part of chr15 ( Pgia8 ) demonstrated mild and transient effect upon arthritis; this effect was PGIA-promoting in males and suppressive in females. Pgia8 and Pgia9 loci demonstrated an additive mode of inheritance, since when they were both incorporated in consomic chr15 strain, the total effect was a sum of the two loci. Using F2 population of the intercross of wild-type and chr15 consomic strain, we confirmed and refined quantitative trait locus positions and identified a strong correlation between disease susceptibility and lymphocyte-producing cytokines of TNF-α and IL-6. Both Pgia8 and Pgia9 loci on chr15 appear to control IL-6 production in spleen cultures of arthritic mice, providing an important link to the mechanism of autoimmune inflammation.
机译:使用蛋白聚糖诱导的关节炎(PGIA),类风湿关节炎的小鼠模型的遗传连锁分析,我们确定了15号染色体(chr15)上的两个基因座Pgia8和Pgia9,似乎与疾病的易感性有关。对易感BALB / c背景中携带完整chr15和分别具有DBA / 2关节炎抗药性的两个基因座中的每个基因座的同类菌株进行免疫接种,确认了chr15上两个基因座的位置:主要Pgia9和次要Pgia8基因座。 Chhr15(Pgia9)的远端部分显示出对雌性PGIA敏感性的主要抑制作用(40%,p <0.001),而该基因座在同基因雄性中的作用仍然显着,但较弱。 chr15(Pgia8)的近端部分对关节炎表现出轻度和短暂的作用;这种作用在男性中促进PGIA,在女性中抑制。 Pgia8和Pgia9基因座显示出遗传的加和模式,因为当将它们都掺入纯净的chr15菌株时,总效果是两个基因座的总和。使用野生型和chr15保育菌株的交配的F2种群,我们确认并完善了数量性状基因座位置,并确定了疾病易感性与TNF-α和IL-6的淋巴细胞生成细胞因子之间的强相关性。 chr15上的Pgia8和Pgia9基因座似乎都可以控制关​​节炎小鼠脾脏培养物中的IL-6产生,为自身免疫炎症机制提供了重要的联系。

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