NMDA receptor-mediated Ca2+ signaling: Impact on cell cycle regulation and the development of neurodegenerative diseases and cancer

兴奋毒性 NMDA受体 神经科学 谷氨酸受体 长期抑郁 受体 程序性细胞死亡 生物 细胞生物学 AMPA受体 细胞凋亡 生物化学
作者
Ana Laura González‐Cota,Daniel Martínez-Flores,Margarita Jacaranda Rosendo‐Pineda,Luis Vaca
出处
期刊:Cell Calcium [Elsevier BV]
卷期号:119: 102856-102856 被引量:27
标识
DOI:10.1016/j.ceca.2024.102856
摘要

NMDA receptors are Ca2+-permeable ligand-gated ion channels that mediate fast excitatory transmission in the central nervous system. NMDA receptors regulate the proliferation and differentiation of neural progenitor cells and also play critical roles in neural plasticity, memory, and learning. In addition to their physiological role, NMDA receptors are also involved in glutamate-mediated excitotoxicity, which results from excessive glutamate stimulation, leading to Ca2+ overload, and ultimately to neuronal death. Thus, NMDA receptor-mediated excitotoxicity has been linked to several neurodegenerative diseases such as Alzheimer's, Parkinson's, Huntington's, dementia, and stroke. Interestingly, in addition to its effects on cell death, aberrant expression or activation of NMDA receptors is also involved in pathological cellular proliferation, and is implicated in the invasion and proliferation of various types of cancer. These disorders are thought to be related to the contribution of NMDA receptors to cell proliferation and cell death through cell cycle modulation. This review aims to discuss the evidence implicating NMDA receptor activity in cell cycle regulation and the link between aberrant NMDA receptor activity and the development of neurodegenerative diseases and cancer due to cell cycle dysregulation. The information presented here will provide insights into the signaling pathways and the contribution of NMDA receptors to these diseases, and suggests that NMDA receptors are promising targets for the prevention and treatment of these diseases, which are leading causes of death and disability worldwide.
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
顾矜应助怡然的凌兰采纳,获得10
刚刚
芷冬发布了新的文献求助10
刚刚
春夏秋冬发布了新的文献求助10
1秒前
awen完成签到,获得积分10
1秒前
远山等故归完成签到,获得积分10
1秒前
2秒前
2秒前
南城忆潇湘完成签到,获得积分10
2秒前
rrjl发布了新的文献求助10
2秒前
鹅鹅鹅应助syn采纳,获得10
2秒前
ccc完成签到,获得积分10
2秒前
敏er给敏er的求助进行了留言
3秒前
槐序二三完成签到,获得积分10
3秒前
852应助不安的依云采纳,获得10
3秒前
蓝幻雷完成签到,获得积分10
3秒前
超帅的勒完成签到,获得积分10
3秒前
PengC完成签到,获得积分10
3秒前
111发布了新的文献求助10
4秒前
xiaolu发布了新的文献求助10
4秒前
一棵草发布了新的文献求助10
4秒前
4秒前
无情的羽毛完成签到,获得积分10
5秒前
369ninja应助哈11采纳,获得10
5秒前
ReAiLeer完成签到,获得积分10
5秒前
czt完成签到,获得积分10
5秒前
修炼成绝完成签到,获得积分10
5秒前
6秒前
852应助王路飞采纳,获得10
6秒前
TanXu完成签到,获得积分10
6秒前
snitch完成签到,获得积分10
6秒前
耍酷谷雪完成签到,获得积分10
7秒前
科研通AI6.2应助我去打球采纳,获得10
7秒前
vikoel完成签到,获得积分10
7秒前
7秒前
pp完成签到,获得积分20
7秒前
高贵树叶发布了新的文献求助30
7秒前
7秒前
YesOK完成签到,获得积分10
7秒前
7秒前
7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
Rosenblum, Global Change Biology 800
自動車の空力技術 800
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 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 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7779149
求助须知:如何正确求助?哪些是违规求助? 9319396
关于积分的说明 20371417
捐赠科研通 7366536
什么是DOI,文献DOI怎么找? 3319361
关于科研通互助平台的介绍 2467388
邀请新用户注册赠送积分活动 2334884