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The role of protein kinase D (PKD) in obesity: Lessons from the heart and other tissues.
Renton, Mark C; McGee, Sean L; Howlett, Kirsten F.
Affiliation
  • Renton MC; Institute for Physical Activity and Nutrition, School of Exercise and Nutrition Science, Deakin University, Geelong, Australia; The Fralin Biomedical Research Institute at Virginia Tech Carilion, Centre for Vascular and Heart Research, Roanoke, VA, USA. Electronic address: mcrenton@vtc.vt.edu.
  • McGee SL; Institute for Mental and Physical Health and Clinical Translation, Metabolic Research Unit, School of Medicine, Deakin University, Geelong, Australia. Electronic address: sean.mcgee@deakin.edu.au.
  • Howlett KF; Institute for Physical Activity and Nutrition, School of Exercise and Nutrition Science, Deakin University, Geelong, Australia. Electronic address: kirsten.howlett@deakin.edu.au.
Biochim Biophys Acta Mol Cell Res ; 1871(7): 119814, 2024 Aug 10.
Article in En | MEDLINE | ID: mdl-39128598
ABSTRACT
Obesity causes a range of tissue dysfunctions that increases the risk for morbidity and mortality. Protein kinase D (PKD) represents a family of stress-activated intracellular signalling proteins that regulate essential processes such as cell proliferation and differentiation, cell survival, and exocytosis. Evidence suggests that PKD regulates the cellular adaptations to the obese environment in metabolically important tissues and drives the development of a variety of diseases. This review explores the role that PKD plays in tissue dysfunction in obesity, with special consideration of the development of obesity-mediated cardiomyopathy, a distinct cardiovascular disease that occurs in the absence of common comorbidities and leads to eventual heart failure and death. The downstream mechanisms mediated by PKD that could contribute to dysfunctions observed in the heart and other metabolically important tissues in obesity, and the predicted cell types involved are discussed to suggest potential targets for the development of therapeutics against obesity-related disease.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biochim Biophys Acta Mol Cell Res Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biochim Biophys Acta Mol Cell Res Year: 2024 Document type: Article