Molecular Relay Stations in Membrane Nanotubes: IRSp53 Involved in Actin-Based Force Generation

Int J Mol Sci. 2023 Aug 23;24(17):13112. doi: 10.3390/ijms241713112.

Abstract

Membrane nanotubes are cell protrusions that grow to tens of micrometres and functionally connect cells. Actin filaments are semi-flexible polymers, and their polymerisation provides force for the formation and growth of membrane nanotubes. The molecular bases for the provision of appropriate force through such long distances are not yet clear. Actin filament bundles are likely involved in these processes; however, even actin bundles weaken when growing over long distances, and there must be a mechanism for their regeneration along the nanotubes. We investigated the possibility of the formation of periodic molecular relay stations along membrane nanotubes by describing the interactions of actin with full-length IRSp53 protein and its N-terminal I-BAR domain. We concluded that I-BAR is involved in the early phase of the formation of cell projections, while IRSp53 is also important for the elongation of protrusions. Considering that IRSp53 binds to the membrane along the nanotubes and nucleates actin polymerisation, we propose that, in membrane nanotubes, IRSp53 establishes molecular relay stations for actin polymerisation and, as a result, supports the generation of force required for the growth of nanotubes.

Keywords: IRSp53; actin; fluorescence microscopy; membrane nanotube; protein–protein interactions.

MeSH terms

  • Actin Cytoskeleton
  • Actins*
  • Animals
  • Cell Membrane Structures
  • Chlorocebus aethiops / metabolism
  • Mice
  • Microvilli
  • Nanotubes*

Substances

  • Actins
  • Baiap2 protein, mouse

Grants and funding

This research was funded by Economic Development and Innovation Operation Programme, Hungary, grant number GINOP-2.3.2-15-2016-00036; New National Excellence Program of the Ministry for Innovation and Technology from the Source of the National Research, Development and Innovation Fund, Hungary, grant number ÚNKP-21-3-II (H.H.); University of Pécs, Medical School, Grant of Dr. Szolcsányi János Research Fund (ÁOK-KA) (E.S.-M.) and Human Resource Development Operational Programme, grant number EFOP 3.6.1-16.2016.00004.