Regulation of intracellular trafficking and secretion of adiponectin by myosin II

Biochem Biophys Res Commun. 2017 Aug 19;490(2):202-208. doi: 10.1016/j.bbrc.2017.06.021. Epub 2017 Jun 9.

Abstract

Adiponectin is a protein secreted by white adipocytes that plays an important role in insulin action, energy homeostasis and the development of atherosclerosis. The intracellular localization and trafficking of GLUT4 and leptin in adipocytes has been well studied, but little is known regarding the intracellular trafficking of adiponectin. Recent studies have demonstrated that constitutive adiponectin secretion is dependent on PIP2 levels and the integrity of cortical F-actin. Non-muscle myosin II is an actin-based motor that is associated with membrane vesicles and participates in vesicular trafficking in mammalian cells. Therefore, we investigated the role of myosin II in the trafficking and secretion of adiponectin in 3T3-L1 adipocytes. Confocal microscopy revealed that myosin IIA and IIB were dispersed throughout the cytoplasm of the adipocyte. Both myosin isoforms were localized in the Golgi/TGN region as evidenced by colocalization with the cis-Golgi marker, p115 and the trans-Golgi marker, γ-adaptin. Inhibition of myosin II activity by blebbistatin or actin depolymerization by latrunculin B dispersed myosin IIA and IIB towards the periphery while significantly inhibiting adiponectin secretion. Therefore, the constitutive trafficking and secretion of adiponectin in 3T3-L1 adipocytes occurs by an actin-dependent mechanism that involves the actin-based motors, myosin IIA and IIB.

Keywords: ER-endoplasmic reticulum; GGA-golgi localizing gamma-adaptin ear homology ARF-binding proteins; GLUT4; PIP2; TGN.

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / drug effects
  • Adipocytes / metabolism
  • Adiponectin / antagonists & inhibitors
  • Adiponectin / metabolism*
  • Animals
  • Biological Transport / drug effects
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Heterocyclic Compounds, 4 or More Rings / pharmacology
  • Mice
  • Nonmuscle Myosin Type IIA / antagonists & inhibitors
  • Nonmuscle Myosin Type IIA / metabolism*
  • Nonmuscle Myosin Type IIB / antagonists & inhibitors
  • Nonmuscle Myosin Type IIB / metabolism*
  • Structure-Activity Relationship
  • Thiazolidines / pharmacology

Substances

  • Adiponectin
  • Adipoq protein, mouse
  • Bridged Bicyclo Compounds, Heterocyclic
  • Heterocyclic Compounds, 4 or More Rings
  • Thiazolidines
  • blebbistatin
  • Nonmuscle Myosin Type IIA
  • Nonmuscle Myosin Type IIB
  • latrunculin B