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胶原诱导关节炎小鼠模型中的基因和蛋白质表达谱。

Gene and Protein Expression Profiles in a Mouse Model of Collagen-Induced Arthritis.

机构信息

Department of Biomedical Laboratory Science, College of Health Science, Eulji University, Seongnam-si, Gyeonggi-do, 13135, Republic of Korea.

Department of Biomedical Laboratory Science, College of Health Sciences, Yonsei University at Wonju, Wonju, Gangwon-do 26493, Republic of Korea.

出版信息

Int J Med Sci. 2018 Jan 1;15(1):77-85. doi: 10.7150/ijms.22345. eCollection 2018.

Abstract

The risk of rheumatoid arthritis (RA), an autoimmune disease, in the elderly population increases along with that of atherosclerosis, cardiovascular disease, type 2 diabetes, and Alzheimer's disease. Identifying specific biomarkers for RA can clarify the underlying molecular mechanisms and can aid diagnosis and patient care. To this end, the present study investigated the genes and proteins that are differentially expressed in RA using a mouse collagen-induced arthritis (CIA) model. We performed gene microarray and proteome array analyses using blood samples from the mice and found that 50 genes and 24 proteins were upregulated and 48 genes were downregulated by more than 2-fold in the CIA model relative to the control. The gene microarray and proteome array results were validated by evaluating the expression levels of select genes and proteins by real-time PCR and western blotting, respectively. We found that the level of integrin α2, which has not been previously reported as a biomarker of RA, was significantly increased in CIA mice as compared to controls. These findings provide a set of novel biomarkers that can be useful for diagnosing and evaluating the progression of RA.

摘要

类风湿关节炎(RA)是一种自身免疫性疾病,其在老年人群中的风险随着动脉粥样硬化、心血管疾病、2 型糖尿病和阿尔茨海默病风险的增加而增加。确定 RA 的特定生物标志物可以阐明潜在的分子机制,并有助于诊断和患者护理。为此,本研究使用小鼠胶原诱导性关节炎(CIA)模型研究了 RA 中差异表达的基因和蛋白质。我们使用来自小鼠的血液样本进行了基因微阵列和蛋白质组阵列分析,发现与对照组相比,CIA 模型中 50 个基因和 24 个蛋白质上调,48 个基因下调超过 2 倍。通过实时 PCR 分别评估选定基因和蛋白质的表达水平,验证了基因微阵列和蛋白质组阵列结果。我们发现,整合素 α2 的水平在 CIA 小鼠中明显高于对照组,而整合素 α2 以前尚未被报道为 RA 的生物标志物。这些发现提供了一组新的生物标志物,可用于诊断和评估 RA 的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9b4/5765742/2c3c2df4577f/ijmsv15p0077g001.jpg

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