A novel in vivo mouse intervertebral disc degeneration model induced by compressive suture

椎间盘 体内 纤维接头 解剖 阿格里坎 变性(医学) 生物 核心 细胞外基质 动物模型 病理 生物医学工程 细胞生物学 医学 骨关节炎 内分泌学 替代医学 生物技术 关节软骨
作者
Zhuochao Liu,Qi Zhou,Jiancheng Zheng,Changwei Li,Weibin Zhang,Xingkai Zhang
出处
期刊:Experimental Cell Research [Elsevier BV]
卷期号:398 (1): 112359-112359 被引量:9
标识
DOI:10.1016/j.yexcr.2020.112359
摘要

Intervertebral disc degeneration (IDD) is the root cause of many musculoskeletal disorders of the spine. However, the etiology of IDD is complex and still not well understood. Animal models of IDD would be useful in deciphering the underlying mechanisms. But the existing animal models have their limitations. Therefore, to establish a novel mouse model that can simulate the human IDD process in vivo, we proposed to carefully circumcise the 2 mm-wide tail skin and then compressively sutured the defect with a simple end-to-end suture to exert excessive pressure on the disc. After 1-week, 2-week, and 4-week compression, the mice were sacrificed and the intervertebral discs were harvested for tissue analysis. The radiological, morphological, and molecular modifications of intervertebral discs were measured to characterize this model. Radiologically, the water content of the intervertebral disc decreased significantly after 2-week compression. Morphologically, the nucleus pulposus showed a decrease in volume and the number of notochordal cells. The compressive suture also broke the balance between anabolic and catabolic enzymes in nucleus pulposus, which led to the remodeling of the extracellular matrix in nucleus pulposus as the content of aggrecan and collagen II decreased. The compressive suture could induce intervertebral discs degeneration in a more reasonable way, which was solely influenced by mechanical loading, as the mice caudal vertebrae still moved freely after the operation. This kind of animal model could be adapted as a reliable in vivo mouse IDD model for the research regarding the etiology and treatments of IDD.
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
tian完成签到 ,获得积分10
刚刚
summor完成签到,获得积分10
刚刚
飞翔的梦完成签到,获得积分10
刚刚
1秒前
鲤鱼宝贝完成签到,获得积分10
1秒前
长脑子的怼怼完成签到 ,获得积分10
1秒前
ZGY发布了新的文献求助10
2秒前
2秒前
悦耳含灵完成签到,获得积分10
3秒前
Lucky完成签到 ,获得积分10
4秒前
hzw完成签到,获得积分10
4秒前
飞天817完成签到,获得积分10
5秒前
6秒前
zhanjl13完成签到,获得积分10
6秒前
泉水激石完成签到,获得积分10
6秒前
Wianiu完成签到,获得积分10
7秒前
8秒前
梁平完成签到 ,获得积分10
8秒前
可乐瓶子完成签到 ,获得积分10
8秒前
萌萌完成签到 ,获得积分10
10秒前
Sandwich发布了新的文献求助10
11秒前
炙热的羽毛完成签到,获得积分10
11秒前
miao123完成签到,获得积分10
11秒前
11秒前
11秒前
11秒前
Kao应助科研通管家采纳,获得10
12秒前
Akim应助张777粒粒采纳,获得10
12秒前
Kao应助科研通管家采纳,获得10
12秒前
snitch完成签到,获得积分10
13秒前
一路向北完成签到,获得积分10
14秒前
东风应助初景采纳,获得10
14秒前
14秒前
15秒前
欧斌完成签到,获得积分10
15秒前
不想喝周完成签到,获得积分10
16秒前
1212完成签到,获得积分10
16秒前
aaa完成签到,获得积分10
17秒前
ajgkd完成签到,获得积分20
17秒前
jasmineyy完成签到 ,获得积分10
17秒前
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
Les chinois de jakarta: temples et vie collective 1000
Autoparametric Resonance in Mechanical Systems 1000
基于锂离子电池正极材料回收的绿色溶剂开发及工程化应用研究 800
Social Psychology 600
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 600
Management and the Arts 510
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 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7646178
求助须知:如何正确求助?哪些是违规求助? 9218446
关于积分的说明 19778513
捐赠科研通 7210600
什么是DOI,文献DOI怎么找? 3276969
关于科研通互助平台的介绍 2438624
邀请新用户注册赠送积分活动 2275052