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George Gerald Rodney Jr.

Rodney Jr.

George Gerald Rodney Jr., Ph.D.

Associate Professor

(713) 798-5797

Positions

Associate Professor
Integrative Physiology
在线黑料门
Houston, TX, US

Education

Post-Doctoral Fellowship at University Of Maryland At Baltimore
01/2004 - Baltimore, Maryland, United States
PhD from Baylor College Of Medicine
01/2001 - Houston, Texas, United States
MS from University Of Texas Health Science Center
01/1996 - San Antonia, Texas, United States

Professional Interests

  • Biomedical Imaging
  • Cardiovascular Sciences
  • Cell and Developmental Biology
  • Human Disease
  • Skeletal Muscle Physiology

Professional Statement

The Rodney Laboratory investigates the cellular and molecular mechanisms that regulate skeletal muscle function, with a primary focus on how alterations in calcium (Ca虏鈦) signaling, redox balance, and intracellular heat production contribute to muscle health and disease. Leveraging more than two decades of expertise in skeletal muscle physiology, the lab combines state-of-the-art imaging technologies鈥攊ncluding confocal microscopy, live-cell calcium imaging, redox biosensors, and organelle-specific thermometry鈥攚ith in vivo and ex vivo functional assessments, biochemical analyses, and histological approaches.

Current research examines how dysregulated Ca虏鈦 handling through the ryanodine receptor (RYR1), oxidative signaling pathways, and mitochondrial function influence muscle performance, aging, congenital myopathies, Duchenne muscular dystrophy, and susceptibility to heat-related illness. Major projects focus on defining the role of sarcoplasmic reticulum Ca虏鈦 leak in muscle physiology and disease, developing gene-editing and allele-suppression therapies for dominant RYR1-associated myopathies, identifying skeletal muscle mechanisms that drive heat stroke and exertional heat stroke, and exploring novel strategies to reduce muscle-generated heat in individuals with ectodermal dysplasia. Collectively, this work seeks to uncover fundamental biological mechanisms governing muscle function while translating these discoveries into innovative therapeutic strategies, including targeted modulation of Ca虏鈦 signaling, genome-editing approaches, and interventions that reduce pathological muscle thermogenesis. These efforts have the potential to improve treatment options for inherited myopathies, muscular dystrophies, heat intolerance disorders, and heat stroke, ultimately enhancing quality of life and clinical outcomes for affected individuals.

Selected Publications

  • Pal,Rituraj; Palmieri,Michela; Loehr,James A.; Li,Shumin; Abo-Zahrah,Reem; Monroe,Tanner O.; Thakur,Poulami B.; Sardiello,Marco; Rodney,George G.. " " Nat Commun. 2014 ; 5 : 5425.
    Pubmed PMID: .
  • Pal,Rituraj; Monroe,Tanner O.; Palmieri,Michela; Sardiello,Marco; Rodney,George G.. " Rotenone induces neurotoxicity through Rac1-dependent activation of NADPH oxidase in SHSY-5Y cells. " FEBS Lett. 2014 Jan ; 588 (3) : 472-481.
  • Pal R, Basu Thakur P, Li S, Minard C, Rodney GG. " " PLoS ONE. 2013 ; 8 (5) : e63989.
    Pubmed PMID: .
  • Lanner JT, Georgiou DK, Dagnino-Acosta A, Ainbinder A, Cheng Q, Joshi AD, Chen Z, Yarotskyy V, Oakes JM, Lee CS, Monroe TO, Santillan A, Dong K, Goodyear L, Ismailov II, Rodney GG, Dirksen RT, Hamilton SL. " " Nat. Med.. 2012 ; 18 (2) : 244-51.
    Pubmed PMID: .

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