Lipid Polarization during Cytokinesis

Cells. 2022 Dec 8;11(24):3977. doi: 10.3390/cells11243977.

Abstract

The plasma membrane of eukaryotic cells is composed of a large number of lipid species that are laterally segregated into functional domains as well as asymmetrically distributed between the outer and inner leaflets. Additionally, the spatial distribution and organization of these lipids dramatically change in response to various cellular states, such as cell division, differentiation, and apoptosis. Division of one cell into two daughter cells is one of the most fundamental requirements for the sustenance of growth in all living organisms. The successful completion of cytokinesis, the final stage of cell division, is critically dependent on the spatial distribution and organization of specific lipids. In this review, we discuss the properties of various lipid species associated with cytokinesis and the mechanisms involved in their polarization, including forward trafficking, endocytic recycling, local synthesis, and cortical flow models. The differences in lipid species requirements and distribution in mitotic vs. male meiotic cells will be discussed. We will concentrate on sphingolipids and phosphatidylinositols because their transbilayer organization and movement may be linked via the cytoskeleton and thus critically regulate various steps of cytokinesis.

Keywords: PUFA; aging; cancer; cataract; ceramide phosphoethanolamine; cholesterol; cortical flow; cytokinesis; disease; endocytic recycling; forward trafficking; lipid polarization; lipids; lowe syndrome; male meiotic cytokinesis; membrane bending; membrane curvature; membrane traffic; multivesicular bodies; multivesicular endosomes; phosphatidic acid; phosphatidyl serine; phosphatidylethanolamine; phosphatidylinositol; phosphatidylinositol phosphates; rab GTPase; sphingolipidoses; sphingolipids; sphingomyelin; transbilayer coupling; triacylglycerols; very long chain fatty acids; very long chain polyunsaturated fatty acids.

Publication types

  • Review
  • Research Support, N.I.H., Intramural

MeSH terms

  • Biological Transport
  • Cell Division
  • Cell Membrane / metabolism
  • Cytokinesis* / physiology
  • Humans
  • Male
  • Phosphatidylinositols* / metabolism

Substances

  • Phosphatidylinositols

Grants and funding

This study was funded by the intramural division of the National Cancer Institute, National Institutes of Health (Division of Health and Human Services). The content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. Government.