NF-κB negatively impacts the myogenic potential of muscle-derived stem cells

Aiping Lu, Jonathan D. Proto, Lulin Guo, Ying Tang, Mitra Lavasani, Jeremy S. Tilstra, Laura J. Niedernhofer, Bing Wang, Denis C. Guttridge, Paul D. Robbins, Johnny Huard

Research output: Contribution to journalArticlepeer-review

52 Scopus citations

Abstract

Inhibition of the inhibitor of kappa B kinase (IKK)/nuclear factor-kappa B (NF-κB) pathway enhances muscle regeneration in injured and diseased skeletal muscle, but it is unclear exactly how this pathway contributes to the regeneration process. In this study, we examined the role of NF-κB in regulating the proliferation and differentiation of muscle-derived stem cells (MDSCs). MDSCs isolated from the skeletal muscles of p65/-mice (haploinsufficient for the p65 subunit of NF-κB) had enhanced proliferation and myogenic differentiation compared to MDSCs isolated from wild-type (wt) littermates. In addition, selective pharmacological inhibition of IKKΒ, an upstream activator of NF-κB, enhanced wt MDSC differentiation into myotubes in vitro. The p65/-MDSCs also displayed a higher muscle regeneration index than wt MDSCs following implantation into adult mice with muscular dystrophy. Additionally, using a muscle injury model, we observed that p65/-MDSC engraftments were associated with reduced inflammation and necrosis. These results suggest that inhibition of the IKK/NF-κB pathway represents an effective approach to improve the myogenic regenerative potential of MDSCs and possibly other adult stem cell populations. Moreover, our results suggest that the improved muscle regeneration observed following inhibition of IKK/NF-κB, is mediated, at least in part, through enhanced stem cell proliferation and myogenic potential.

Original languageEnglish (US)
Pages (from-to)661-668
Number of pages8
JournalMolecular Therapy
Volume20
Issue number3
DOIs
StatePublished - Mar 2012
Externally publishedYes

Bibliographical note

Funding Information:
The authors thank the members of the Huard Laboratory, especially Jenny Zhu and Bin Sun for discussions and technical advice. Special thanks go to Joseph Feduska and Bridget Deasy for live cell imaging advice. This work was supported in part by the Henry J. Mankin Endowed Chair for Orthopedic Research at the University of Pittsburgh, the William F. and Jean W. Donaldson Chair at Children's Hospital of Pittsburgh. L.J.N. is supported by NIEHS (ES016114) and NIA (AG033907). The authors do not have conflicts of interest to disclose other than the corresponding author who receives consulting fees from Cook MyoSite Inc.

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