Mitochondria in neurodegeneration: Investigating the role of mitochondria and metabolism in the cause and therapeutic targeting of neurodegenerative diseases
Mitochondria in neurodegeneration: Investigating the role of mitochondria and metabolism in the cause and therapeutic targeting of neurodegenerative diseases
批准号:
MC_UU_00028/6
负责人:
Alexander Whitworth
金额:
$382.26万
依托单位:
依托单位国家:
英国
项目类别:
Intramural
财政年份:
2022
资助国家:
英国
项目状态:
未结题
起止时间:
2022 至 --
中文摘要
点击翻译按钮获取中文摘要
英文摘要
The survival of our most active tissues, such as the brain and heart, throughout decades of a human lifespan presents an extraordinary biological challenge. The cellular organelles known as mitochondria are central to the life and death of these tissues. While providing the high amount of energy required by these cells and buffering cytoplasmic calcium flux, they also produce many of the molecules that cause cellular damage and house an array of cell death-inducing factors. Thus, these organelles require extensive maintenance and quality control processes. Failure in mitochondrial homeostasis is strongly linked to age-related conditions such as neurodegeneration.Our group aims to understand the mechanisms of mitochondrial homeostasis in relation to neurodegenerative diseases such as Parkinson’s disease and motor neuron disease. We use a combination of the powerful genetic techniques of Drosophila (fruit flies) and molecular, cell biology and biochemical approaches in mammalian cells. Insights into these mechanisms will deliver a greater understanding of the role of mitochondrial maintenance in the health and dysfunction of the nervous system in a physiological context and will help guide therapeutic development to combat neurodegenerative diseases.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
FBXO7/ntc and USP30 antagonistically set the ubiquitination threshold for basal mitophagy and provides a target for Pink1 phosphorylation in vivo
FBXO7/ntc 和 USP30 拮抗地设定基础线粒体自噬的泛素化阈值,并为 Pink1 体内磷酸化提供靶点
DOI:
10.1101/2022.10.10.511602
发表时间:
2022
期刊:
影响因子:
--
作者:
[Sanchez-Martinez A]
通讯作者:
Sanchez-Martinez A
DOI:
10.1016/j.nbd.2022.105941
发表时间:
2023-01-01
期刊:
Neurobiology of disease
影响因子:
6.1
作者:
[De Lazzari, Federica, Agostini, Francesco, Bisaglia, Marco]
通讯作者:
Bisaglia, Marco
DOI:
10.3390/cells12081143
发表时间:
2023-04-13
期刊:
Cells
影响因子:
6
作者:
[]
通讯作者:
DOI:
10.7554/elife.84424
发表时间:
2023-01-09
期刊:
ELIFE
影响因子:
7.7
作者:
[Agip, Ahmed-Noor A., Chung, Injae, Sanchez-Martinez, Alvaro, Whitworth, Alexander J., Hirst, Judy]
通讯作者:
Hirst, Judy
DOI:
10.15252/embr.202153552
发表时间:
2022-12-06
期刊:
EMBO reports
影响因子:
7.7
作者:
[]
通讯作者:
共 8 条
JAK-STAT immune signalling in PINK1-related Parkinson's disease
-
批准号:MR/X008142/1
-
项目类别:Research Grant
-
资助金额:$51.28万
-
财政年份:2023
-
负责人:Alexander Whitworth
-
依托单位:
The role of axonal mRNA translation in Amyotrophic Lateral Sclerosis (resubmission)
-
批准号:MR/V003933/1
-
项目类别:Research Grant
-
资助金额:$48.34万
-
财政年份:2020
-
负责人:Alexander Whitworth
-
依托单位:
国内基金
海外基金
登录
查看更多内容
探索PRAK与ARPC2的潜在相互作用及其在细胞自噬介导的神经萎缩中的功能和相关机制
-
批准号:32000522
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2020
-
负责人:刘佩佩
-
依托单位:
C9ORF72-SMCR8复合物在小胶质细胞中的功能及其介导的炎症反应
-
批准号:32070743
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2020
-
负责人:杨玫
-
依托单位:
ESCRT蛋白Vps4在神经损伤引起的轴突自噬和沃勒变性中的作用和机制研究
-
批准号:31970697
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2019
-
负责人:方燕姗
-
依托单位:
Vici综合征致病基因Epg5自噬缺陷的高通量筛选
-
批准号:31900533
-
项目类别:青年科学基金项目
-
资助金额:26.0万元
-
批准年份:2019
-
负责人:郑巧霞
-
依托单位:
酸性鞘磷脂酶缺陷导致神经退行性病变的分子机制
-
批准号:30700219
-
项目类别:青年科学基金项目
-
资助金额:19.0万元
-
批准年份:2007
-
负责人:刘忠华
-
依托单位: