Literature DB >> 32744761

αV integrins in Schwann cells promote attachment to axons, but are dispensable in vivo.

Kathleen K Catignas1,2, Luciana R Frick1,3, Marta Pellegatta1,4, Edward Hurley1,3, Zachary Kolb2, Kathryn Addabbo2, Joseph H McCarty5, Richard O Hynes6, Arjan van der Flier6,7, Yannick Poitelon1,2,8, Lawrence Wrabetz1,2,3, Maria Laura Feltri1,2,3.   

Abstract

In the developing peripheral nervous system, Schwann cells (SCs) extend their processes to contact, sort, and myelinate axons. The mechanisms that contribute to the interaction between SCs and axons are just beginning to be elucidated. Using a SC-neuron coculture system, we demonstrate that Arg-Gly-Asp (RGD) peptides that inhibit αV -containing integrins delay the extension of SCs elongating on axons. αV integrins in SC localize to sites of contact with axons and are expressed early in development during radial sorting and myelination. Short interfering RNA-mediated knockdown of the αV integrin subunit also delays SC extension along axons in vitro, suggesting that αV -containing integrins participate in axo-glial interactions. However, mice lacking the αV subunit in SCs, alone or in combination with the potentially compensating α5 subunit, or the αV partners β3 or β8 , myelinate normally during development and remyelinate normally after nerve crush, indicating that overlapping or compensatory mechanisms may hide the in vivo role of RGD-binding integrins.
© 2020 Wiley Periodicals LLC.

Entities:  

Keywords:  RGD; Schwann cell; axo-glial interactions; integrin; lamellipodia; process extension

Mesh:

Substances:

Year:  2020        PMID: 32744761      PMCID: PMC8491627          DOI: 10.1002/glia.23886

Source DB:  PubMed          Journal:  Glia        ISSN: 0894-1491            Impact factor:   7.452


  94 in total

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