Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

TNFα reverse signaling promotes sympathetic axon growth and target innervation

Kisiswa, Lilian ORCID: https://orcid.org/0000-0002-1800-0645, Osório, Catarina Raquel, Erice Jurecky, Clara, Vizard, Thomas Neill, Wyatt, Sean Lee ORCID: https://orcid.org/0000-0002-0572-234X and Davies, Alun M. ORCID: https://orcid.org/0000-0001-5841-8176 2013. TNFα reverse signaling promotes sympathetic axon growth and target innervation. Nature Neuroscience 16 (7) , pp. 865-873. 10.1038/nn.3430

Full text not available from this repository.

Abstract

Reverse signaling via members of the tumor necrosis factor (TNF) superfamily controls multiple aspects of immune function. Here we document TNFα reverse signaling in the nervous system to our knowledge for the first time and show that it has a crucial role in establishing sympathetic innervation. During postnatal development, sympathetic axons express TNFα as they grow and branch in their target tissues, which in turn express TNF receptor 1 (TNFR1). In culture, soluble forms of TNFR1 act directly on postnatal sympathetic axons to promote growth and branching by a mechanism that depends on membrane-integrated TNFα and on downstream activation of ERK. Sympathetic innervation density is substantially lower in several tissues in postnatal and adult mice lacking either TNFα or TNFR1. These findings reveal that target-derived TNFR1 acts as a reverse-signaling ligand for membrane-integrated TNFα to promote growth and branching of sympathetic axons.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Biosciences
Subjects: Q Science > QH Natural history > QH301 Biology
Q Science > QH Natural history > QH426 Genetics
Publisher: Nature Publishing Group
ISSN: 1097-6256
Last Modified: 24 Oct 2022 11:34
URI: https://orca.cardiff.ac.uk/id/eprint/48604

Citation Data

Cited 49 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item Edit Item