Reduced Expression of Septin7 Hinders Skeletal Muscle Regeneration

Author:

Szabó László123,Telek Andrea1ORCID,Fodor János1,Dobrosi Nóra13,Dócs Klaudia4,Hegyi Zoltán4ORCID,Gönczi Mónika13ORCID,Csernoch László13ORCID,Dienes Beatrix1ORCID

Affiliation:

1. Department of Physiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary

2. Doctoral School of Molecular Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary

3. ELKH-DE Cell Physiology Research Group, University of Debrecen, 4032 Debrecen, Hungary

4. Department of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary

Abstract

Septins are considered the fourth component of the cytoskeleton with the septin7 isoform playing a critical role in the formation of diffusion barriers in phospholipid bilayers and intra- and extracellular scaffolds. While its importance has already been confirmed in different intracellular processes, very little is known about its role in skeletal muscle. Muscle regeneration was studied in a Sept7 conditional knock-down mouse model to prove the possible role of septin7 in this process. Sterile inflammation in skeletal muscle was induced which was followed by regeneration resulting in the upregulation of septin7 expression. Partial knock-down of Sept7 resulted in an increased number of inflammatory cells and myofibers containing central nuclei. Taken together, our data suggest that partial knock-down of Sept7 hinders the kinetics of muscle regeneration, indicating its crucial role in skeletal muscle functions.

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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