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Qa-2 在单纯疱疹病毒诱导的 Behcet 病样小鼠模型中的作用,Qa-2 是 HLA-G 的功能同源物。

The role of Qa-2, the functional homolog of HLA-G, in a Behcet's disease-like mouse model induced by the herpes virus simplex.

机构信息

Laboratory of Cell Biology, Ajou University Institute for Medical Sciences, Suwon, Korea.

Department of Biology, Sungshin University, Seoul, Korea.

出版信息

J Inflamm (Lond). 2010 Jun 24;7:31. doi: 10.1186/1476-9255-7-31.

DOI:10.1186/1476-9255-7-31
PMID:20573271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2902457/
Abstract

BACKGROUND

It has been suggested that the HLA-G molecule is a genetic risk factor for Behcet's disease (BD). In this study, we evaluated the level of Qa-2, a murine nonclassical class I MHC molecule and possible functional homolog of HLA-G, to determine if it was associated with various symptoms of BD-like mice. In addition, we investigated siRNA (small interfering RNA) treatment to determine if it inhibited Qa-2 expression, thereby changing the symptoms of mice.

METHODS

RNA interference (RNAi) and vector transfection were employed to manipulate gene expression in vivo in mice. siRNA (small interfering RNA) or Qa-2 expression vector was applied to inhibit or up-regulate Qa-2 expression, respectively.

RESULTS

The Qa-2 levels in granulocytes were lower in BD-like mice than in normal controls. The silencing of Qa-2 by intravenous injection of siRNA (500 nmol/mouse, 4 times at 3-day intervals) specifically reduced the Qa-2 levels and worsened the BD-like symptoms.

CONCLUSIONS

Silencing Qa-2 by injecting siRNA into mice resulted in deterioration of symptoms in BD-like mice.

摘要

背景

有人提出 HLA-G 分子是白塞病 (BD) 的遗传风险因素。在这项研究中,我们评估了 Qa-2 的水平,Qa-2 是一种鼠类非经典 I 类 MHC 分子,可能是 HLA-G 的功能同源物,以确定它是否与类似 BD 的小鼠的各种症状有关。此外,我们研究了 siRNA(小干扰 RNA)治疗,以确定它是否抑制了 Qa-2 的表达,从而改变了小鼠的症状。

方法

采用 RNA 干扰 (RNAi) 和载体转染技术在体内操纵小鼠的基因表达。用 siRNA(小干扰 RNA)或 Qa-2 表达载体分别抑制或上调 Qa-2 的表达。

结果

类似 BD 的小鼠中性粒细胞中的 Qa-2 水平低于正常对照。静脉注射 siRNA(500nmol/只,每 3 天注射 4 次)可特异性沉默 Qa-2,降低 Qa-2 水平并加重类似 BD 的症状。

结论

向小鼠体内注射 siRNA 沉默 Qa-2 可导致类似 BD 的小鼠症状恶化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/62e547a23f1f/1476-9255-7-31-9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/9952254a767a/1476-9255-7-31-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/31ffea762ad1/1476-9255-7-31-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/059a99551aea/1476-9255-7-31-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/13109138a234/1476-9255-7-31-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/253f12378402/1476-9255-7-31-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/28a8f478697d/1476-9255-7-31-7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/95c4587d014d/1476-9255-7-31-8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/62e547a23f1f/1476-9255-7-31-9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/9952254a767a/1476-9255-7-31-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/31ffea762ad1/1476-9255-7-31-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/059a99551aea/1476-9255-7-31-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/13109138a234/1476-9255-7-31-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/253f12378402/1476-9255-7-31-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/28a8f478697d/1476-9255-7-31-7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/95c4587d014d/1476-9255-7-31-8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a77/2902457/62e547a23f1f/1476-9255-7-31-9.jpg

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