The experimental study of mir‐99a‐5p negative regulation of TLR8 receptor mediated‐mediated innate immune response in rabbit knee cartilage injury

先天免疫系统 软骨 免疫系统 骨关节炎 医学 细胞生物学 受体 免疫学 模式识别受体 生物 癌症研究 病理 解剖 内科学 替代医学
作者
Jiebin Zhang,Ke Zheng,Yichao Wu,Shengting Zhang,Ao Guo,Cong Sui
出处
期刊:Immunity, inflammation and disease [Wiley]
卷期号:12 (4) 被引量:2
标识
DOI:10.1002/iid3.1211
摘要

Abstract Background Traumatic cartilage injury is an important cause of osteoarthritis (OA) and limb disability, and toll‐like receptors (TLRs) mediated innate immune response has been confirmed to play a crucial role in cartilage injury. In the previous study, we found that the activation of TLR8 molecules in injured articular cartilage was more obvious than other TLRs by establishing an animal model of knee impact injury in rabbits, and the changes of TLR8 molecules could significantly affect the process of articular cartilage injury and repair. Objective To verify how mir‐99a‐5p regulates TLR8 receptor mediated innate immune response to treat traumatic cartilage injury. Methods The impact of a heavy object on the medial condyle of the rabbit's knee joint caused damage to the medial condylar cartilage. Through pathological and imaging analysis, it was demonstrated whether the establishment of an animal model of traumatic cartilage injury was successful. Establishing a cell model by virus transfection of chondrocytes to demonstrate the role of TLR8 in the innate immune response to impact cartilage injury. Through transcriptome sequencing, potential targets of TLR8, mir‐99a‐5p, were predicted, and basic experiments were conducted to demonstrate how they interact with innate immune responses to impact cartilage damage. Results TLR8 is a receptor protein of the immune system, which is widely expressed in immune cells. In our study, we found that TLR8 expression is localized in lysosomes and endosomes. Mir‐99a‐5p can negatively regulate TLR8 to activate PI3K‐AKT molecular pathway and aggravate cartilage damage. Inhibiting TLR8 expression can effectively reduce the incidence of articular cartilage damage. Conclusion Based on the results from this study, mir‐99a‐5p may be an effective molecular marker for predicting traumatic cartilage injury and targeting TLR8 is a novel and promising approach for the prevention or early treatment of cartilage damage.
最长约 10秒,即可获得该文献文件

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
香蕉觅云应助gomm采纳,获得10
刚刚
科研通AI5应助fufu采纳,获得10
1秒前
sfef发布了新的文献求助10
1秒前
XIL发布了新的文献求助10
1秒前
田様应助油赞子采纳,获得10
1秒前
完美世界应助迷路的翠阳采纳,获得30
1秒前
1秒前
tuzhifengyin完成签到,获得积分10
1秒前
2秒前
2秒前
OUDIE发布了新的文献求助10
3秒前
晏清发布了新的文献求助10
3秒前
研友_ED5GK完成签到,获得积分0
4秒前
听话的萤完成签到,获得积分10
4秒前
GGKing发布了新的文献求助10
4秒前
5秒前
张津浩完成签到,获得积分0
5秒前
LZJ发布了新的文献求助10
5秒前
丘比特应助JHL采纳,获得10
5秒前
暴富发布了新的文献求助10
5秒前
nnnd77发布了新的文献求助10
6秒前
谨慎青亦发布了新的文献求助10
6秒前
壳壳完成签到,获得积分10
6秒前
7秒前
7秒前
Ziyi_Xu完成签到,获得积分10
7秒前
乐风完成签到,获得积分10
8秒前
SYLH应助alexyang采纳,获得10
8秒前
OIIII应助程程采纳,获得10
8秒前
chu完成签到,获得积分10
8秒前
彭于彦祖应助姜且采纳,获得20
8秒前
SYLH应助Zhang1867采纳,获得20
9秒前
所所应助ihtw采纳,获得10
9秒前
合适忆之发布了新的文献求助10
9秒前
一帆风顺发布了新的文献求助10
9秒前
泡泡发布了新的文献求助10
10秒前
帕尼灬尼完成签到,获得积分10
10秒前
Verdigris完成签到,获得积分10
11秒前
斯文的斩发布了新的文献求助10
11秒前
安东尼奥完成签到,获得积分10
11秒前
高分求助中
Java: A Beginner's Guide, 10th Edition 5000
Applied Survey Data Analysis (第三版, 2025) 800
Narcissistic Personality Disorder 700
Research Handbook on Multiculturalism 500
The Martian climate revisited: atmosphere and environment of a desert planet 500
Plasmonics 400
建国初期十七年翻译活动的实证研究. 建国初期十七年翻译活动的实证研究 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3848400
求助须知:如何正确求助?哪些是违规求助? 3391110
关于积分的说明 10565539
捐赠科研通 3111610
什么是DOI,文献DOI怎么找? 1714836
邀请新用户注册赠送积分活动 825498
科研通“疑难数据库(出版商)”最低求助积分说明 775556