Logo image
Axonal amphoterin mRNA is regulated by translational control and enhances axon outgrowth
Journal article   Open access   Peer reviewed

Axonal amphoterin mRNA is regulated by translational control and enhances axon outgrowth

Tanuja T Merianda, Jennifer Coleman, Hak Hee Kim, Pabitra Kumar Sahoo, Cynthia Gomes, Paul Brito-Vargas, Heikki Rauvala, Armin Blesch, Soonmoon Yoo and Jeffery L Twiss
The Journal of neuroscience, v 35(14), pp 5693-5706
08 Apr 2015
PMID: 25855182
url
https://doi.org/10.1523/jneurosci.3397-14.2015View
Published, Version of Record (VoR)CC BY-NC-SA V4.0 Open

Abstract

3' Untranslated Regions - genetics Animals Axons - drug effects Axons - metabolism Biological Transport - genetics Cells, Cultured Ganglia, Spinal - cytology Gene Expression Regulation - genetics Green Fluorescent Proteins - genetics Green Fluorescent Proteins - metabolism HMGB1 Protein - genetics HMGB1 Protein - metabolism Male Microtubule-Associated Proteins - genetics Microtubule-Associated Proteins - metabolism Photobleaching Protein Biosynthesis - genetics Rats Rats, Sprague-Dawley RNA, Messenger - metabolism RNA, Small Interfering - pharmacology Sensory Receptor Cells - cytology Sensory Receptor Cells - drug effects Transduction, Genetic
High mobility group (HMG) proteins concentrate in the nucleus, interacting with chromatin. Amphoterin is an HMG protein (HMGB1) that has been shown to have extranuclear functions and can be secreted from some cell types. Exogenous amphoterin can increase neurite growth, suggesting that the secreted protein may have growth promoting activities in neurons. Consistent with this, we show that depletion of amphoterin mRNA from cultured adult rat DRG neurons attenuates neurite outgrowth, pointing to autocrine or paracrine mechanisms for its growth-promoting effects. The mRNA encoding amphoterin localizes to axonal processes and we showed recently that its 3'-UTR is sufficient for axonal localization of heterologous transcripts (Donnelly et al., 2013). Here, we show that amphoterin mRNA is transported constitutively into axons of adult DRG neurons. A preconditioning nerve injury increases the levels of amphoterin protein in axons without a corresponding increase in amphoterin mRNA in the axons. A 60 nucleotide region of the amphoterin mRNA 3'-UTR is necessary and sufficient for its localization into axons of cultured sensory neurons. Amphoterin mRNA 3'-UTR is also sufficient for axonal localization in distal axons of DRG neurons in vivo. Overexpression of axonally targeted amphoterin mRNA increases axon outgrowth in cultured sensory neurons, but axon growth is not affected when the overexpressed mRNA is restricted to the cell body.

Metrics

3 Record Views
28 citations in Scopus

Details

UN Sustainable Development Goals (SDGs)

This publication has contributed to the advancement of the following goals:

#3 Good Health and Well-Being

InCites Highlights

Data related to this publication, from InCites Benchmarking & Analytics tool:

Collaboration types
Domestic collaboration
International collaboration
Web of Science research areas
Neurosciences
Logo image