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Publication : Isolated Plin5-deficient cardiomyocytes store less lipid droplets than normal, but without increased sensitivity to hypoxia.

First Author  Li Y Year  2021
Journal  Biochim Biophys Acta Mol Cell Biol Lipids Volume  1866
Issue  4 Pages  158873
PubMed ID  33373698 Mgi Jnum  J:301535
Mgi Id  MGI:6505070 Doi  10.1016/j.bbalip.2020.158873
Citation  Li Y, et al. (2020) Isolated Plin5-deficient cardiomyocytes store less lipid droplets than normal, but without increased sensitivity to hypoxia. Biochim Biophys Acta Mol Cell Biol Lipids 1866(4):158873
abstractText  Plin5 is abundantly expressed in the heart where it binds to lipid droplets (LDs) and facilitates physical interaction between LDs and mitochondria. We isolated cardiomyocytes from adult Plin5(+/+) and Plin5(-/-) mice to study the role of Plin5 for fatty acid uptake, LD accumulation, fatty acid oxidation, and tolerance to hypoxia. Cardiomyocytes isolated from Plin5(-/-) mice cultured with oleic acid stored less LDs than Plin5(+/+), but comparable levels to Plin5(+/+) cardiomyocytes when adipose triglyceride lipase activity was inhibited. The ability to oxidize fatty acids into CO2 was similar between Plin5(+/+) and Plin5(-/-) cardiomyocytes, but Plin5(-/-) cardiomyocytes had a transient increase in intracellular fatty acid oxidation intermediates. After pre-incubation with oleic acids, Plin5(-/-) cardiomyocytes retained a higher content of glycogen and showed improved tolerance to hypoxia compared to Plin5(+/+). In isolated, perfused hearts, deletion of Plin5 had no important effect on ventricular pressures or infarct size after ischemia. Old Plin5(-/-) mice had reduced levels of cardiac triacylglycerides, increased heart weight, and apart from modest elevated expression of mRNAs for beta myosin heavy chain Myh7 and the fatty acid transporter Cd36, other genes involved in fatty acid oxidation, glycogen metabolism and glucose utilization were essentially unchanged by removal of Plin5. Plin5 seems to facilitate cardiac LD storage primarily by repressing adipose triglyceride lipase activity without altering cardiac fatty acid oxidation capacity. Expression of Plin5 and cardiac LD content of isolated cardiomyocytes has little importance for tolerance to acute hypoxia and ischemia, which contrasts the protective role for Plin5 in mouse models during myocardial ischemia.
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