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X染色体上的基因影响小鼠胶原诱导性关节炎的发展。

Genes on the X chromosome affect development of collagen-induced arthritis in mice.

作者信息

Jansson L, Holmdahl R

机构信息

Department of Medical and Physiological Chemistry, Uppsala University, Sweden.

出版信息

Clin Exp Immunol. 1993 Dec;94(3):459-65. doi: 10.1111/j.1365-2249.1993.tb08218.x.

Abstract

Susceptibility to collagen-induced arthritis (CIA) in mice is associated with a class II gene in MHC (Aq) but also with unknown genes outside MHC. Investigated here is the influence of genes on the X chromosome as well as the role of the X-linked immunodeficiency (xid) mutation. Reciprocal male F1 hybrids, bred to be heterozygous or homozygous for Aq, showed a genetic influence in their susceptibility to develop CIA. Crosses were made between B10.G, B10.Q, DBA/1, SWR/J, C3H.Q and CBA/Ca, and all F1 mice were castrated to avoid sex hormone modulation of the susceptibility. A differential timing of arthritis onset and severity were seen in the reciprocal F1 males. An exception was the reciprocal F1 male offspring from SWR/J and DBA/1 crosses which differed only in disease severity late in the course of the disease. The female F1 crosses did not show the same pattern of differential susceptibility to CIA as the F1 males. To exclude the possible influence of the Y chromosome, F1 males of reciprocal crosses were back-crossed to the parental strains creating offspring with equal X chromosomes but divergent Y chromosomes. No difference in development of arthritis was observed in these. The influence of the xid mutation was investigated next. The xid loci from the CBA/N mouse was bred into DBA/1 strain which is highly susceptible to CIA. The resulting congenic DBA/1-xid strain was resistant to induction of CIA and did not develop an antibody response to type II collagen. We conclude that polymorphic genes on the X chromosome modulate susceptibility to CIA. The results from the experiments with mice carrying xid mutations confirm that such immune modulating genes exist on the sex chromosomes.

摘要

小鼠对胶原诱导性关节炎(CIA)的易感性与MHC中的II类基因(Aq)相关,但也与MHC外的未知基因有关。本文研究了X染色体上基因的影响以及X连锁免疫缺陷(xid)突变的作用。相互杂交的雄性F1杂种,培育成Aq杂合或纯合子,在其患CIA的易感性方面表现出遗传影响。在B10.G、B10.Q、DBA/1、SWR/J、C3H.Q和CBA/Ca之间进行杂交,所有F1小鼠均被阉割以避免性激素对易感性的调节。在相互杂交的F1雄性小鼠中观察到关节炎发病时间和严重程度的差异。一个例外是SWR/J和DBA/1杂交产生的相互杂交F1雄性后代,它们仅在疾病后期的严重程度上有所不同。雌性F1杂交小鼠对CIA的易感性差异模式与雄性F1小鼠不同。为了排除Y染色体的可能影响,将相互杂交的F1雄性小鼠回交至亲本品系,产生具有相等X染色体但不同Y染色体的后代。在这些后代中未观察到关节炎发展的差异。接下来研究了xid突变的影响。将CBA/N小鼠的xid基因座导入对CIA高度易感的DBA/1品系。产生的同源DBA/1-xid品系对CIA诱导具有抗性,并且对II型胶原没有产生抗体反应。我们得出结论,X染色体上的多态性基因调节对CIA的易感性。携带xid突变的小鼠实验结果证实,这种免疫调节基因存在于性染色体上。

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