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Ciliary Hedgehog signaling during adult tissue repair and disease

成人组织修复和疾病期间的睫状刺猬信号传导

基本信息

批准号：
10599347
负责人：
Daniel Kopinke
金额：
$ 35.18万
依托单位：
UNIVERSITY OF FLORIDA
依托单位国家：
美国
项目类别：
财政年份：
2022
资助国家：
美国
起止时间：
2022-04-01 至 2027-03-31
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10599347
关键词：
Acute Address Adipocytes Adult Affect Ants Biological Assay Biology Cells Chronic Cicatrix Cilia Coculture Techniques Data Development Diabetes Mellitus Direct Lytic Factors Disease Duchenne muscular dystrophy Endothelial Cells Equilibrium Erinaceidae Fatty acid glycerol esters Fibrosis Genetic Glycerol Goals Health Histology In Vitro Infiltration Injury Intramuscular Knowledge Ligands Measurement Modeling Molecular Muscle Muscle function Muscle satellite cell Muscular Atrophy Myopathy Natural regeneration Neuromuscular Diseases Obesity Outcome Pathogenicity Pathway interactions Positioning Attribute Publishing Regenerative capacity Reporting Role SHH gene Schwann Cells Signal Pathway Signal Transduction System Testing Time Tissues Work age related cell type combat experimental study human disease improved in vivo innovation insight intercellular communication interstitial knockout animal lipid biosynthesis mdx mouse mouse model muscle form muscle regeneration muscle strength myogenesis novel novel therapeutic intervention pharmacologic preservation prevent progenitor repaired sarcopenia skeletal muscle wasting smoothened signaling pathway therapeutic development tissue repair tool

项目摘要

Project Summary Fatty fibrosis, the replacement of healthy muscle tissue with fat and fibrotic scar tissue, is a prominent feature of chronic muscle diseases such as Duchenne muscular dystrophy (DMD), sarcopenia, the age-related loss of skeletal muscle and strength, in addition to obesity, and diabetes. This project will identify and characterize the cellular and molecular mechanisms by which intramuscular fat forms, and the functional consequences of intramuscular fat on muscle health. Recent evidence points to ciliary Hedgehog signaling as a potent ant- adipogenic signal during muscle regeneration and in mdx mice, a mouse model of DMD. In addition, Hedgehog promotes muscle repair and prevents the decline in myofiber size in mdx mice. By what mechanism(s) Hedgehog acts to balance fat formation and muscle regeneration is unknown. This proposal will use innovative and powerful mouse models to identify the role of Hedgehog signaling during muscle regeneration in the following aims: 1) Identify and characterize the responsible Hedgehog ligand; 2) determine which cell types respond to Hedgehog signaling; and 3) demonstrate if intramuscular fat directly affects muscle health. Taken together, this proposal will provide insights into the origin and function of intramuscular fat and will aid in the search for novel therapeutic interventions into human diseases affected by fatty fibrosis.

项目总结