Investigating the role of C9orf72 in autophagic and metabolic dysregulation in ALS/FTD

研究 C9orf72 在 ALS/FTD 自噬和代谢失调中的作用

基本信息

批准号：
10606605
负责人：
Jiou Wang
金额：
$ 56.75万
依托单位：
JOHNS HOPKINS UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2015
资助国家：
美国
起止时间：
2015-05-15 至 2025-04-30
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10606605
关键词：
ALS pathology Address Aging Alzheimer&apos s Disease Amyotrophic Lateral Sclerosis Autophagocytosis Biochemical Biological Models Brain C9ORF72 Caenorhabditis elegans Cells Clinical Defect Dementia Disease Elderly Equilibrium Etiology FRAP1 gene Feedback Frontotemporal Dementia Genes Genetic Genetic study Goals Guanosine Triphosphate Phosphohydrolases Homeostasis Huntington Disease Intervention Investigation Knowledge Link Lysosomes Metabolic Metabolic Control Metabolic Pathway Metabolism Molecular Motor Neurons Mutation Nerve Degeneration Neurodegenerative Disorders Nucleotides Organelles Pathogenesis Pathology Pathway interactions Patients Physiological Play Predisposition Proteins Public Health Quality Control Regulation Research Role Signal Transduction Societies Spinal Cord System Temporal Lobe Tissues Toxic effect Untranslated RNA Work c9FTD/ALS cell growth regulation coactivator-associated arginine methyltransferase 1 effective therapy epigenetic regulation frontal lobe frontotemporal lobar dementia amyotrophic lateral sclerosis genetic approach insight lipid metabolism loss of function neurotoxicity news novel novel strategies novel therapeutic intervention sporadic amyotrophic lateral sclerosis tool treatment strategy

项目摘要

Neurodegeneration is an increasing public health issue and remains an unsolved biomedical challenge. Genetic discoveries have provided news avenues for investigating the molecular mechanisms of several neurodegenerative diseases. Recently, a hexanucleotide repeat expansion in a noncoding region of the C9orf72 gene was linked to the neurodegenerative disease amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). ALS is characterized by loss of motor neurons, and the C9orf72 mutation represents the most common genetic cause of both familial and sporadic ALS. FTD is characterized by degeneration of the frontal and temporal lobes of the brain and is the second most common type of dementia for people older than 65; the C9orf72 mutation is also the most common genetic causes for FTD. The C9orf72 mutation is also found to contribute to Alzheimer’s disease and Huntington’s disease. Despite intense efforts and rapid advances, our understanding of the disease mechanisms and treatment strategies for C9orf72-linked ALS/FTD are still at the early stages. To help relieve the public health burden associated with these diseases, it is important to understand the mechanisms underlying the pathogenesis. We have recently discovered that C9orf72 plays an important role in the regulation of autophagy and related metabolic processes, suggesting that further studies of C9orf72 functions could shed light on the mechanism of ALS/FTD pathogenesis. The goal of the proposed project is to elucidate the mechanisms through which dysregulation of C9orf72 functions leads to molecular defects and neuronal toxicity. The specific aims are to identify the central mechanisms through which C9orf72 regulates autophagy and related metabolism, to delineate the pathways through which the pathogenesis is generated, and to identify potential intervention strategies. The proposed studies, which combine biochemical, molecular, and genetic approaches, are expected to provide insight into fundamental mechanisms of neurodegeneration in ALS/FTD that may ultimately leads to novel approaches for treating these devastating neurodegenerative diseases.

神经退行性疾病是一个日益严重的公共卫生问题，并且仍然是一个尚未解决的问题生物医学挑战。基因发现为研究这一问题提供了新闻途径。最近，一种六核苷酸研究了几种神经退行性疾病的分子机制。 C9orf72 基因非编码区的重复扩增与神经退行性疾病肌萎缩侧索硬化症 (ALS) 和额颞叶痴呆 (FTD)。 ALS 的特点是运动神经元丧失，C9orf72 突变代表了运动神经元的丧失。家族性和散发性 ALS 最常见的遗传原因是 FTD。大脑额叶和颞叶的退化是第二常见的 65 岁以上人群的痴呆症类型；C9orf72 突变也是最常见的 FTD 的遗传原因也被发现与阿尔茨海默病有关。尽管付出了巨大的努力并取得了快速的进展，但我们对亨廷顿舞蹈症的了解仍然有限。 C9orf72相关的ALS/FTD的疾病机制和治疗策略仍处于早期阶段为了帮助减轻与这些疾病相关的公共卫生负担，这一点很重要。为了了解发病机制，我们最近发现了这一点。 C9orf72在自噬及相关代谢过程的调节中发挥重要作用，表明对 C9orf72 功能的进一步研究可以揭示其机制该项目的目标是阐明 ALS/FTD 的发病机制。 C9orf72 功能失调会导致分子缺陷和神经缺陷具体目标是确定 C9orf72 的中心机制。调节自噬和相关代谢，以描绘自噬和相关代谢的途径产生发病机制，并确定潜在的干预策略。结合生化、分子和遗传学方法的研究预计将深入了解 ALS/FTD 神经退行性变的基本机制，可能最终导致治疗这些破坏性神经退行性疾病的新方法。

项目成果

期刊论文数量（21）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Autophagy as a common pathway in amyotrophic lateral sclerosis.

DOI：
10.1016/j.neulet.2018.04.006
发表时间：
2019-04-01
期刊：
Neuroscience letters
影响因子：
2.5
作者：
Nguyen DKH;Thombre R;Wang J
通讯作者：
Wang J

Cell-type specific differences in promoter activity of the ALS-linked C9orf72 mouse ortholog.

DOI：
10.1038/s41598-017-05864-2
发表时间：
2017-07-18
期刊：
Scientific reports
影响因子：
4.6
作者：
Langseth AJ;Kim J;Ugolino JE;Shah Y;Hwang HY;Wang J;Bergles DE;Brown SP
通讯作者：
Brown SP

USP7 regulates ALS-associated proteotoxicity and quality control through the NEDD4L-SMAD pathway.

DOI：
10.1073/pnas.2014349117
发表时间：
2020-11-10
期刊：
Proceedings of the National Academy of Sciences of the United States of America
影响因子：
11.1
作者：
Zhang T;Periz G;Lu YN;Wang J
通讯作者：
Wang J

A Helicase Unwinds Hexanucleotide Repeat RNA G-Quadruplexes and Facilitates Repeat-Associated Non-AUG Translation.

DOI：
10.1021/jacs.1c00131
发表时间：
2021-05-19
期刊：
Journal of the American Chemical Society
影响因子：
15
作者：
Liu H;Lu YN;Paul T;Periz G;Banco MT;Ferré-D'Amaré AR;Rothstein JD;Hayes LR;Myong S;Wang J
通讯作者：
Wang J

Heterochronic Phenotype Analysis of Hypodermal Seam Cells in Caenorhabditis elegans.

秀丽隐杆线虫皮下接缝细胞的异时表型分析。