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Slamf1,即自然杀伤T细胞控制基因Nkt1。

Slamf1, the NKT cell control gene Nkt1.

作者信息

Jordan Margaret A, Fletcher Julie M, Pellicci Daniel, Baxter Alan G

机构信息

Comparative Genomics Center, James Cook University, Townsville, Queensland, Australia.

出版信息

J Immunol. 2007 Feb 1;178(3):1618-27. doi: 10.4049/jimmunol.178.3.1618.

Abstract

Invariant NKT cells play a critical role in controlling the strength and character of adaptive immune responses. We have previously reported deficiencies in the numbers and function of NKT cells in the NOD mouse strain, which is a well-validated model of type 1 diabetes and systemic lupus erythematosus. Genetic control of thymic NKT cell numbers was mapped to two linkage regions: Nkt1 on distal chromosome 1 and Nkt2 on chromosome 2. In this study, we report the production and characterization of a NOD.Nkrp1(b).Nkt1(b) congenic mouse strain, apply microarray expression analyses to limit candidate genes within the 95% confidence region, identify Slamf1 (encoding signaling lymphocyte activation molecule) and Slamf6 (encoding Ly108) as potential candidates, and demonstrate retarded signaling lymphocyte activation molecule expression during T cell development of NOD mice, resulting in reduced expression at the CD4(+)CD8(+) stage, which is consistent with decreased NKT cell production and deranged tolerance induction in NOD mice.

摘要

不变自然杀伤T细胞在控制适应性免疫反应的强度和特征方面发挥着关键作用。我们之前报道过,非肥胖糖尿病(NOD)小鼠品系中自然杀伤T细胞的数量和功能存在缺陷,该品系是1型糖尿病和系统性红斑狼疮的有效模型。胸腺自然杀伤T细胞数量的遗传控制被定位到两个连锁区域:位于远端1号染色体上的Nkt1和2号染色体上的Nkt2。在本研究中,我们报告了NOD.Nkrp1(b).Nkt1(b)同源近交系小鼠品系的产生和特征,应用微阵列表达分析来限定95%置信区间内的候选基因,确定信号淋巴细胞激活分子家族1(编码信号淋巴细胞激活分子)和信号淋巴细胞激活分子家族6(编码Ly108)为潜在候选基因,并证明在NOD小鼠的T细胞发育过程中信号淋巴细胞激活分子表达延迟,导致在CD4(+)CD8(+)阶段表达降低,这与NOD小鼠中自然杀伤T细胞产生减少和耐受性诱导紊乱一致。

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