Rab18 binds PLIN2 and ACSL3 to mediate lipid droplet dynamics

Biochim Biophys Acta Mol Cell Biol Lipids. 2021 Jul;1866(7):158923. doi: 10.1016/j.bbalip.2021.158923. Epub 2021 Mar 11.

Abstract

Lipid droplet (LD) is a vital organelle governing lipid homeostasis and Rab18 has been linked to lipid metabolism. However, the mechanisms of Rab18-mediated LD dynamics in myoblast cells remain elusive. Here, we report that Rab18 plays an important role in oleic acid (OA)-induced LD accumulation in mouse myoblast C2C12 cells. Rab18 was translocated from the endoplasmic reticulum (ER) to LDs during LD accumulation, which was regulated by perilipin 2 (PLIN2), a major LD protein. LD-associated Rab18 bound with the C terminus of PLIN2 and the LD localization of Rab18 was diminished when PLIN2 was depleted. Moreover, loss of function of Rab18 led to reduced triacylglycerol (TAG) level and fewer but larger LDs. In contrast, overexpression of Rab18 resulted in elevated TAG content and LD number. Furthermore, LD-associated Rab18 interacted with acyl-CoA synthetase long-chain family member 3 (ACSL3), which in turn promoted the LD localization of this protein. These data show that Rab18 interacts with PLIN2 and forms a complex with PLIN2 and ACSL3, which plays a critical role in LD accumulation and dynamics of myoblast cells.

Keywords: ACSL3; Lipid droplets; PLIN2; Rab18; TAG.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Coenzyme A Ligases / metabolism*
  • Lipid Droplets / metabolism*
  • Mice
  • Perilipin-2 / metabolism*
  • Protein Binding
  • rab GTP-Binding Proteins / metabolism*

Substances

  • Perilipin-2
  • Rab18 protein, mouse
  • rab GTP-Binding Proteins
  • Acsl3 protein, mouse
  • Coenzyme A Ligases