Griseti_2023_FEBS.Lett__

Reference

Title : Molecular mechanisms of perilipin protein function in lipid droplet metabolism - Griseti_2023_FEBS.Lett__
Author(s) : Griseti E , Bello AA , Bieth E , Sabbagh B , Iacovoni JS , Bigay J , Laurell H , Copic A
Ref : FEBS Letters , : , 2023
Abstract :

Perilipins are abundant lipid droplet (LD) proteins present in all metazoans, and also in amoebozoa and fungi. Humans express five perilipins, which share a similar domain organization: an amino-terminal PAT domain and an 11-mer repeat region, which can fold into amphipathic helices that interact with LDs, followed by a structured carboxy-terminal domain. Variations of this organization that arose during vertebrate evolution allow for functional specialization between perilipins in relation to metabolic needs of different tissues. We discuss how different features of perilipins influence their interaction with LDs and their cellular targeting. PLIN1 and PLIN5 play a direct role in lipolysis by regulating the recruitment of lipases to LDs and LD interaction with mitochondria. Other perilipins, particularly PLIN2, appear to protect LDs from lipolysis, but the molecular mechanism is not clear. PLIN4 stands out with its long repetitive region, whereas PLIN3 is most widely expressed and is used as a nascent LD marker. Finally, we discuss the genetic variability in perilipins in connection with metabolic disease, prominent for PLIN1 and PLIN4, underlying the importance of understanding the molecular function of perilipins.

PubMedSearch : Griseti_2023_FEBS.Lett__
PubMedID: 38140813

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Citations formats

Griseti E, Bello AA, Bieth E, Sabbagh B, Iacovoni JS, Bigay J, Laurell H, Copic A (2023)
Molecular mechanisms of perilipin protein function in lipid droplet metabolism
FEBS Letters :

Griseti E, Bello AA, Bieth E, Sabbagh B, Iacovoni JS, Bigay J, Laurell H, Copic A (2023)
FEBS Letters :