Front. Physiol. Frontiers in Physiology Front. Physiol. 1664-042X Frontiers Media S.A. 10.3389/fphys.2017.00886 Physiology Correction Corrigendum: G-CSF does not influence C2C12 myogenesis despite receptor expression in healthy and dystrophic skeletal muscle Wright Craig R. 1 Brown Erin L. 1 Della-Gatta Paul A. 1 Ward Alister C. 2 Lynch Gordon S. 3 Russell Aaron P. 1 * 1Centre for Physical Activity and Nutrition, School of Exercise and Nutrition Sciences, Deakin University, Burwood, VIC, Australia 2Molecular and Medical Research SRC, School of Medicine, Deakin University, Waurn Ponds, VIC, Australia 3Basic and Clinical Myology Laboratory, Department of Physiology, The University of Melbourne, VIC, Australia

Edited by: Steven P. Jones, University of Louisville, United States

Reviewed by: Frontiers Physiology Editorial Office, Frontiers Media SA, Switzerland; Bradford G. Hill, University of Louisville, United States

*Correspondence: Aaron P. Russell aaron.russell@deakin.edu.au

This article was submitted to Striated Muscle Physiology, a section of the journal Frontiers in Physiology

 30 10 2017 2017 8 886 24 09 2017 19 10 2017 Copyright © 2017 Wright, Brown, Della-Gatta, Ward, Lynch and Russell. 2017 Wright, Brown, Della-Gatta, Ward, Lynch and Russell

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

 A corrigendum on G-CSF does not influence C2C12 myogenesis despite receptor expression in healthy and dystrophic skeletal muscle by Wright, C. R., Brown, E. L., Della-Gatta, P. A., Ward, A. C., Lynch, G. S., and Russell, A. P. (2014). Front. Physiol. 5:170. doi: 10.3389/fphys.2014.00170 G-CSF cytokine receptor skeletal muscle duchenne muscular dystrophy mdx C2C12 proliferation differentiation

In the original article, there was a mistake in Figure 1. Identification of G-CSFR in human and rodent skeletal muscle, as published. The mistake is found in part 1A of the figure which should show that PCR product from mouse tissues (left hand image) and human tissues (right hand image). Unfortunately, when preparing the image the right hand agarose gel image that was embedded is the same as the left hand image. The corrected Figure 1 and figure legend appears below. The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way.

Identification of G-CSFR in rodent and human skeletal muscle. (A) cDNA fragment amplified during Real Time-PCR using the primers described in Table 1, separated on a 1.8% Sybr safe (Invitrogen) agarose gel and exposed to UV light. (B) Western blot image identifying G-CSFR in rodent and human skeletal muscle in vitro and ex vivo. (C) Western blot for G-CSFR in positive (BAF/3[G]) and negative (293T) control cells. (D) G-CSFR after deglycosylation with PGNase. C2B (C2C12 myoblasts), C2T (C2C12 myotubes), Dia (diaphragm muscle from C57BLK mice), TA (tibialis anterior muscle from C57BLK mice), HpB (human primary myoblasts), HpT (human primary myotubes) HVL (human vastus lateralis muscle), BAF/3[G] (murine pro B cell line overexpressing G-CSFR), 293T (human embryonic kidney 293T cell line), 1kb+ [1 kb plus ladder (Invitrogen) and WB (Whole blood (human)].

 Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The reviewer BGH and handling Editor declared their shared affiliation.