| Literature DB >> 29459438 |
Alessio Colombo1, Hung-En Hsia1,2, Mengzhe Wang3, Peer-Hendrik Kuhn2, Monika S Brill3, Paolo Canevazzi4, Regina Feederle1,5,6, Carla Taveggia4, Thomas Misgeld1,3,6,7, Stefan F Lichtenthaler8,2,6.
Abstract
Death receptor 6 (DR6) is an orphan member of the TNF receptor superfamily and controls cell death and differentiation in a cell-autonomous manner in different cell types. Here, we report an additional non-cell-autonomous function for DR6 in the peripheral nervous system (PNS). DR6-knockout (DR6 KO) mice showed precocious myelination in the PNS Using an in vitro myelination assay, we demonstrate that neuronal DR6 acts in trans on Schwann cells (SCs) and reduces SC proliferation and myelination independently of its cytoplasmic death domain. Mechanistically, DR6 was found to be cleaved in neurons by "a disintegrin and metalloprotease 10" (ADAM10), releasing the soluble DR6 ectodomain (sDR6). Notably, in the in vitro myelination assay, sDR6 was sufficient to rescue the DR6 KO phenotype. Thus, in addition to the cell-autonomous receptor function of full-length DR6, the proteolytically released sDR6 can unexpectedly also act as a paracrine signaling factor in the PNS in a non-cell-autonomous manner during SC proliferation and myelination. This new mode of DR6 signaling will be relevant in future attempts to target DR6 in disease settings.Entities:
Keywords: ADAM10; DR6; Schwann cell; myelin; shedding
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Year: 2018 PMID: 29459438 PMCID: PMC5881626 DOI: 10.15252/embj.201797390
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598