Accumulation of glucosylceramide in the absence of the beta-glucosidase GBA2 alters cytoskeletal dynamics

PLoS Genet. 2015 Mar 24;11(3):e1005063. doi: 10.1371/journal.pgen.1005063. eCollection 2015 Mar.

Abstract

Glycosphingolipids are key elements of cellular membranes, thereby, controlling a variety of cellular functions. Accumulation of the simple glycosphingolipid glucosylceramide results in life-threatening lipid storage-diseases or in male infertility. How glucosylceramide regulates cellular processes is ill defined. Here, we reveal that glucosylceramide accumulation in GBA2 knockout-mice alters cytoskeletal dynamics due to a more ordered lipid organization in the plasma membrane. In dermal fibroblasts, accumulation of glucosylceramide augments actin polymerization and promotes microtubules persistence, resulting in a higher number of filopodia and lamellipodia and longer microtubules. Similar cytoskeletal defects were observed in male germ and Sertoli cells from GBA2 knockout-mice. In particular, the organization of F-actin structures in the ectoplasmic specialization and microtubules in the sperm manchette is affected. Thus, glucosylceramide regulates cytoskeletal dynamics, providing mechanistic insights into how glucosylceramide controls signaling pathways not only during sperm development, but also in other cell types.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / chemistry
  • Actins / metabolism*
  • Animals
  • Cell Membrane / metabolism
  • Cell Membrane / pathology
  • Cytoskeleton / genetics*
  • Cytoskeleton / metabolism
  • Cytoskeleton / pathology
  • Fibroblasts / metabolism
  • Glucosylceramides / chemistry
  • Glucosylceramides / genetics*
  • Glucosylceramides / metabolism
  • Humans
  • Lipid Metabolism / genetics*
  • Male
  • Mice
  • Mice, Knockout
  • Microtubules / genetics
  • Microtubules / metabolism
  • Microtubules / pathology
  • Pseudopodia / genetics
  • Pseudopodia / metabolism
  • Pseudopodia / pathology
  • Sertoli Cells / metabolism
  • Sertoli Cells / pathology
  • beta-Glucosidase / genetics*
  • beta-Glucosidase / metabolism

Substances

  • Actins
  • Glucosylceramides
  • beta-Glucosidase
  • beta-glucosidase 2, mouse

Grants and funding

The work was funded by the German Research Foundation (SFB 645 to DW, PD, KS), the Maria von Linden Program, University of Bonn (DW), and a Minerva Research Group to DW. DW and FB are members of the Bonn Excellence Cluster ImmunoSensation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.