Glycolipid transfer protein knockout disrupts vesicle trafficking to the plasma membrane

J Biol Chem. 2023 Apr;299(4):104607. doi: 10.1016/j.jbc.2023.104607. Epub 2023 Mar 15.

Abstract

The glycolipid transfer protein (GLTP) has been linked to many cellular processes aside from its best-known in vitro function as a lipid transport protein. It has been proposed to act as a sensor and regulator of glycosphingolipid homeostasis in cells. Furthermore, through its previously determined interaction with the endoplasmic reticulum membrane protein VAP-A (vesicle-associated membrane protein-associated protein A), GLTP may also be involved in facilitating vesicular transport in cells. In this study, we characterized the phenotype of CRISPR/Cas9-mediated GLTP KO HeLa cells. We showed that motility, three-dimensional growth, and cellular metabolism were all altered by GLTP knockout. Expression of a GLTP mutant incapable of binding VAP disrupted cell spheroid formation, indicating that the GLTP-VAP interaction is linked to cellular adhesion, cohesion, and three-dimensional growth. Most notably, we found evidence that GLTP, through its interaction with VAP-A, affects vesicular trafficking, marking the first cellular process discovered to be directly impacted by a change in GLTP expression.

Keywords: Golgi; VAP-A; VSVG; endoplasmic reticulum (ER); gene silencing; glycerosphingolipid; glycolipid; intracellular trafficking; lipid transport; sphingolipid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Transport* / genetics
  • Carrier Proteins* / genetics
  • Carrier Proteins* / metabolism
  • Cell Membrane* / metabolism
  • Cell Movement / genetics
  • Cytosol / metabolism
  • Gene Expression Regulation / genetics
  • Gene Knockout Techniques
  • HeLa Cells
  • Humans
  • Protein Binding / genetics

Substances

  • Carrier Proteins
  • lipid transfer protein
  • VAPA protein, human