Septin 7 reduces nonmuscle myosin IIA activity in the SNAP23 complex and hinders GLUT4 storage vesicle docking and fusion

Exp Cell Res. 2017 Jan 15;350(2):336-348. doi: 10.1016/j.yexcr.2016.12.010. Epub 2016 Dec 20.

Abstract

Glomerular epithelial cells, podocytes, are insulin responsive and can develop insulin resistance. Here, we demonstrate that the small GTPase septin 7 forms a complex with nonmuscle myosin heavy chain IIA (NMHC-IIA; encoded by MYH9), a component of the nonmuscle myosin IIA (NM-IIA) hexameric complex. We observed that knockdown of NMHC-IIA decreases insulin-stimulated glucose uptake into podocytes. Both septin 7 and NM-IIA associate with SNAP23, a SNARE protein involved in GLUT4 storage vesicle (GSV) docking and fusion with the plasma membrane. We observed that insulin decreases the level of septin 7 and increases the activity of NM-IIA in the SNAP23 complex, as visualized by increased phosphorylation of myosin regulatory light chain. Also knockdown of septin 7 increases the activity of NM-IIA in the complex. The activity of NM-IIA is increased in diabetic rat glomeruli and cultured human podocytes exposed to macroalbuminuric sera from patients with type 1 diabetes. Collectively, the data suggest that the activity of NM-IIA in the SNAP23 complex plays a key role in insulin-stimulated glucose uptake into podocytes. Furthermore, we observed that septin 7 reduces the activity of NM-IIA in the SNAP23 complex and thereby hinders GSV docking and fusion with the plasma membrane.

Keywords: GLUT4 storage vesicle; Glucose uptake; Nonmuscle myosin IIA; Podocytes; SNARE; Septin 7.

MeSH terms

  • Animals
  • Diabetes Mellitus, Type 1 / metabolism*
  • Diabetic Nephropathies / metabolism*
  • Epithelial Cells / metabolism
  • Glucose / metabolism
  • Glucose Transporter Type 4 / metabolism*
  • HEK293 Cells
  • Humans
  • Insulin / metabolism
  • Kidney Tubules / metabolism
  • Mice
  • Nonmuscle Myosin Type IIA / metabolism*
  • Podocytes / metabolism
  • Rats
  • Septins / genetics
  • Septins / metabolism*
  • Transport Vesicles / metabolism*
  • Vesicular Transport Proteins / metabolism*

Substances

  • Glucose Transporter Type 4
  • Insulin
  • Vesicular Transport Proteins
  • Nonmuscle Myosin Type IIA
  • Septins
  • Glucose