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Open Access Research

Krüppel-like factor 6 (KLF6) promotes cell proliferation in skeletal myoblasts in response to TGFβ/Smad3 signaling

Mathew G Dionyssiou1, Jahan Salma124, Mariya Bevzyuk1, Stephanie Wales1, Lusine Zakharyan1 and John C McDermott1234*

Author Affiliations

1 Department of Biology, York University; York University, 4700 Keele St, Toronto, ON, M3J 1P3, Canada

2 Centre for Research in Mass Spectrometry, York University; York University, Toronto, ON, M3J 1P3, Canada

3 Muscle Health Research Centre, York University; York University, Toronto, ON, M3J 1P3, Canada

4 Centre for Research in Biomolecular Interactions, York University; York University, Toronto, ON, M3J 1P3, Canada

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Skeletal Muscle 2013, 3:7  doi:10.1186/2044-5040-3-7

Published: 2 April 2013

Abstract

Background

Krüppel-like factor 6 (KLF6) has been recently identified as a MEF2D target gene involved in neuronal cell survival. In addition, KLF6 and TGFβ have been shown to regulate each other’s expression in non-myogenic cell types. Since MEF2D and TGFβ also fulfill crucial roles in skeletal myogenesis, we wanted to identify whether KLF6 functions in a myogenic context.

Methods

KLF6 protein expression levels and promoter activity were analyzed using standard cellular and molecular techniques in cell culture.

Results

We found that KLF6 and MEF2D are co-localized in the nuclei of mononucleated but not multinucleated myogenic cells and, that the MEF2 cis element is a key component of the KLF6 promoter region. In addition, TGFβ potently enhanced KLF6 protein levels and this effect was repressed by pharmacological inhibition of Smad3. Interestingly, pharmacological inhibition of MEK/ERK (1/2) signaling resulted in re-activation of the differentiation program in myoblasts treated with TGFβ, which is ordinarily repressed by TGFβ treatment. Conversely, MEK/ERK (1/2) inhibition had no effect on TGFβ-induced KLF6 expression whereas Smad3 inhibition negated this effect, together supporting the existence of two separable arms of TGFβ signaling in myogenic cells. Loss of function analysis using siRNA-mediated KLF6 depletion resulted in enhanced myogenic differentiation whereas TGFβ stimulation of myoblast proliferation was reduced in KLF6 depleted cells.

Conclusions

Collectively these data implicate KLF6 in myoblast proliferation and survival in response to TGFβ with consequences for our understanding of muscle development and a variety of muscle pathologies.

Keywords:
Myoblasts; Krüppel-like factor 6; Transforming growth factor β; Cell proliferation