亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

Overexpression of miR-31 in Peripheral Blood Mononuclear Cells (PBMC) from Patients with Ankylosing Spondylitis

外周血单个核细胞 小RNA 和平号-155 强直性脊柱炎 免疫学 医学 自身免疫 逆转录聚合酶链式反应 实时聚合酶链反应 内科学 生物 抗体 信使核糖核酸 基因 体外 生物化学
作者
Mengmeng Wang,Li Wang,Xu Zhang,Xiao Yang,Xiaona Li,Qing Xia,Mengya Chen,Renfang Han,Rui Liu,Shengqian Xu,Faming Pan
出处
期刊:Medical Science Monitor [International Scientific Information Inc.]
卷期号:23: 5488-5494 被引量:14
标识
DOI:10.12659/msm.905238
摘要

BACKGROUND:miRNAs play vital roles in regulating immunologic functions and autoimmunity. However, the levels of miR-31, miR-155, miR-16, and miR-181a have not been explored in AS, but were verified to play vital roles in other immunological diseases. The aim of our study was to examine whether the expressions of miR-31, miR-155, miR-16, and miR-181a are abnormal in AS. MATERIAL AND METHODS:Real-time transcription-polymerase chain reaction analysis (RT-PCR) was used to determine the expression of miR-31, miR-155, miR-16, and miR-181a in peripheral blood mononuclear cells (PBMC) from 40 patients with AS and 40 healthy controls. RESULTS:The expression of miR-31 was increased in AS patients compared with healthy controls (p=0.001). Furthermore, we detected no significant differences in the expressions of miR-155, miR-16, and miR-181a between AS patients and healthy controls. However, the expression levels of the 4 miRNAs were all significantly different between less active AS and more active AS, with higher levels in more active AS. Moreover, no significant correlations were found between the 4 miRNAs levels with the clinical characteristics in the patients with AS. Interestingly, the expression levels of miR-31, miR-155, and miR-16 in PBMCs were significantly positively correlated with the ESR in new AS patients but not old AS patients. CONCLUSIONS:Our results suggest that miR-31 is overexpressed in PBMCs of AS patients. Furthermore, miR-31, miR-155, miR-16 and miR-181a may be associated with AS disease activity.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Gongl完成签到,获得积分10
7秒前
7秒前
852应助duoduo烤红薯采纳,获得10
10秒前
iShine完成签到 ,获得积分10
12秒前
大大撒发布了新的文献求助10
14秒前
15秒前
16秒前
科研通AI2S应助科研通管家采纳,获得30
20秒前
慕青应助科研通管家采纳,获得10
20秒前
Ethan发布了新的文献求助50
21秒前
诺曦完成签到,获得积分10
21秒前
科研通AI6.2应助sherry采纳,获得30
21秒前
阿昊关注了科研通微信公众号
22秒前
28秒前
31秒前
32秒前
李李发布了新的文献求助10
34秒前
36秒前
脾中完成签到 ,获得积分10
37秒前
38秒前
Qin应助Jodie采纳,获得30
41秒前
48秒前
领导范儿应助活泼的元菱采纳,获得10
50秒前
刘天歌完成签到 ,获得积分10
55秒前
小丸子发布了新的文献求助10
55秒前
1分钟前
干净的琦应助小丸子采纳,获得10
1分钟前
duoduo烤红薯完成签到 ,获得积分10
1分钟前
淡然的山水完成签到,获得积分10
1分钟前
无聊的金针菇完成签到,获得积分20
1分钟前
lijunliang完成签到,获得积分10
1分钟前
冷傲书萱完成签到,获得积分10
1分钟前
冷傲书萱发布了新的文献求助10
1分钟前
完美世界应助大气大侠采纳,获得10
1分钟前
Asteria发布了新的文献求助30
1分钟前
2分钟前
大气大侠完成签到,获得积分10
2分钟前
2分钟前
[刘小婷]完成签到,获得积分10
2分钟前
2分钟前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Prompt Engineering for Clinicians: Harnessing AI in Everyday Medical Practice 600
REAL-WORLD EFFICACY AND GENOMIC LANDSCAPE OF POLATUZUMA VEDOTIN-BASED FIRST-LINE THERAPY IN DIFFUSE LARGE B-CELL LYMPHOMA: A FOCUS ON TP53 MUTATIONS AND TREATMENT RESPONSE 500
Handbook of Luminescence Dating 500
Safety Pharmacology 500
《KNN基无铅压电陶瓷电学性能优化与物理机理研究》 500
Elgar Concise Encyclopedia of Space Law 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6945906
求助须知:如何正确求助?哪些是违规求助? 8631107
关于积分的说明 18306682
捐赠科研通 6382569
什么是DOI,文献DOI怎么找? 3079895
关于科研通互助平台的介绍 2121741
邀请新用户注册赠送积分活动 2056826