Exploration of the mode of death and potential death mechanisms of nucleus pulposus cells

上睑下垂 程序性细胞死亡 坏死性下垂 变性(医学) 衰老 生物 椎间盘 细胞凋亡 死因 炎症 细胞生物学 生物信息学 神经科学 医学 疾病 病理 免疫学 遗传学 解剖
作者
Daqian Zhou,Yongliang Mei,Chao Song,Kang Cheng,Weiye Cai,Daru Guo,Silong Gao,Jiale Lv,Tao Liu,Yang Zhou,Liquan Wang,Bing Liu,Zongchao Liu
出处
期刊:European Journal of Clinical Investigation [Wiley]
卷期号:54 (9): e14226-e14226 被引量:31
标识
DOI:10.1111/eci.14226
摘要

Intervertebral disc degeneration (IVDD) is a common chronic orthopaedic disease in orthopaedics that imposes a heavy economic burden on people and society. Although it is well established that IVDD is associated with genetic susceptibility, ageing and obesity, its pathogenesis remains incompletely understood. Previously, IVDD was thought to occur because of excessive mechanical loading leading to destruction of nucleus pulposus cells (NPCs), but studies have shown that IVDD is a much more complex process associated with inflammation, metabolic factors and NPCs death and can involve all parts of the disc, characterized by causing NPCs death and extracellular matrix (ECM) degradation. The damage pattern of NPCs in IVDD is like that of some programmed cell death, suggesting that IVDD is associated with programmed cell death. Although apoptosis and pyroptosis of NPCs have been studied in IVDD, the pathogenesis of intervertebral disc degeneration can still not be fully elucidated by using only traditional cell death modalities. With increasing research, some new modes of cell death, PANoptosis, ferroptosis and senescence have been found to be closely related to intervertebral disc degeneration. Among these, PANoptosis combines essential elements of pyroptosis, apoptosis and necroptosis to form a highly coordinated and dynamically balanced programmed inflammatory cell death process. Furthermore, we believe that PANoptosis may also crosstalk with pyroptosis and senescence. Therefore, we review the progress of research on multiple deaths of NPCs in IVDD to provide guidance for clinical treatment.
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
刚刚
飞快的聪展完成签到,获得积分10
刚刚
宇麦达发布了新的文献求助10
刚刚
dochx完成签到,获得积分10
1秒前
忽远忽近的她完成签到 ,获得积分10
2秒前
WYN完成签到,获得积分10
3秒前
wu完成签到,获得积分10
4秒前
海皇星空完成签到 ,获得积分10
4秒前
77完成签到,获得积分10
4秒前
zzk发布了新的文献求助10
5秒前
6秒前
yyy完成签到,获得积分10
7秒前
7秒前
科研达人发布了新的文献求助10
7秒前
8秒前
yjf,123完成签到 ,获得积分10
8秒前
海盗船长完成签到,获得积分10
9秒前
Hey完成签到 ,获得积分10
9秒前
solidtimingg关注了科研通微信公众号
10秒前
gaoww完成签到,获得积分10
10秒前
可知完成签到,获得积分20
11秒前
11秒前
yang发布了新的文献求助10
12秒前
饕餮发布了新的文献求助10
12秒前
虎虎虎呼呼完成签到,获得积分10
14秒前
15秒前
称心的伟泽关注了科研通微信公众号
15秒前
背后的小白菜完成签到,获得积分10
16秒前
16秒前
矢思然发布了新的文献求助10
17秒前
19秒前
一只孙小忆完成签到,获得积分10
19秒前
Crazyer完成签到,获得积分10
19秒前
Richardxuuu完成签到,获得积分10
19秒前
李卓完成签到,获得积分10
20秒前
冷艳的班完成签到,获得积分10
20秒前
星辰大海应助Sean采纳,获得10
20秒前
SciGPT应助Vincent采纳,获得10
21秒前
矢思然完成签到,获得积分10
21秒前
可恶大怂包完成签到,获得积分10
21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
2026年中国辛酸癸酸聚乙二醇甘油酯行业市场规模及竞争格局分析报告 1000
48V Low-voltage Power Distribution Network (PDN) Architecture Industry Report, 2024 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 610
适配Micro-LED色转换的高兼容性量子点负性光刻胶制备与工艺研究 500
Direct and Iterative Linear System Solvers 500
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 7312778
求助须知:如何正确求助?哪些是违规求助? 8929267
关于积分的说明 18924483
捐赠科研通 6973336
什么是DOI,文献DOI怎么找? 3213476
关于科研通互助平台的介绍 2381597
邀请新用户注册赠送积分活动 2191537