Open AccessGDE3 regulates oligodendrocyte precursor proliferation via release of soluble CNTFRα
Author(s) -
Mateusz Dobrowolski,
Clinton Cave,
Reuben Levy-Myers,
ChangHee Lee,
Sung Jin Park,
Bo Ran Choi,
Bo Xiao,
Wanchun Yang,
Shanthini Sockanathan
Publication year - 2020
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.180695
Subject(s) - ciliary neurotrophic factor , biology , microbiology and biotechnology , oligodendrocyte , growth factor , regulator , signal transduction , receptor , neurotrophic factors , biochemistry , neuroscience , myelin , central nervous system , gene
Oligodendrocyte development is tightly controlled by extrinsic signals; however, mechanisms that modulate cellular responses to these factors remain unclear. Six-transmembrane glycerophosphodiester phosphodiesterases (GDEs) are emerging as central regulators of cellular differentiation via their ability to shed glycosylphosphatidylinositol (GPI)-anchored proteins from the cell surface. We show here that GDE3 controls the pace of oligodendrocyte generation by negatively regulating oligodendrocyte precursor cell (OPC) proliferation. GDE3 inhibits OPC proliferation by stimulating ciliary neurotrophic factor (CNTF)-mediated signaling through release of CNTFRα, the ligand-binding component of the CNTF-receptor multiprotein complex, which can function as a soluble factor to activate CNTF signaling. GDE3 releases soluble CNTFRα by GPI-anchor cleavage from the plasma membrane and from extracellular vesicles (EVs) after co-recruitment of CNTFRα in EVs. These studies uncover new physiological roles for GDE3 in gliogenesis and identify GDE3 as a key regulator of CNTF-dependent regulation of OPC proliferation through release of CNTFRα.