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Profiling of human myotubes reveals an intrinsic proteomic signature associated with type 2 diabetes
KTH, Skolan för bioteknologi (BIO), Industriell bioteknologi. (Cell Technology Group)
Vise andre og tillknytning
2014 (engelsk)Inngår i: Translational Proteomics, ISSN 2212-9634, Vol. 2, nr 1, s. 25-38Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The development of insulin resistance and type 2 diabetes (T2D) involves a complex array of metabolic defects in skeletal muscle. An in vitro cell culture system excludes the acute effects of external systemic factors existing in vivo. Thus, we aimed to determine whether intrinsic differences in the protein profile exist in cultured myotubes derived from T2D versus normal glucose tolerant (NGT) healthy people. Applying two dimensional difference gel electrophoresis technology (2-D DIGE), the abundance of 47 proteins differed in myotubes derived from T2D patients versus NGT donors. Proteins involved in fatty acid and amino acid metabolism, TCA cycle, mitochondrial function, mRNA processing, DNA repair and cell survival showed higher abundance, while proteins associated with redox signaling (PARK7; Parkinson disease 7), glutathione metabolism (glutathione S-transferase, GST, isoforms T1, P1 and M2), and protein dynamics (heat shock protein, HSP, isoform B1 and 90A) showed reduced abundance in myotubes derived from T2D versus NGT donors. Consistent with our proteome analysis results, the level of total glutathione was reduced in myotubes obtained from T2D versus NGT donors. Taken together, our data provide evidence for intrinsic differences in the profile of proteins involved in energy metabolism, cellular oxidative stress, protein dynamics and gene regulation in myotubes derived from T2D patients. These differences thereby suggest a genetic or epigenetic influence on protein content level, which can be further investigated to understand the molecular underpinnings of T2D progression and lead to new therapeutic approaches.

sted, utgiver, år, opplag, sider
2014. Vol. 2, nr 1, s. 25-38
Emneord [en]
Cytoskeleton, Gene regulation, In vitro, Metabolism, Oxidative stress defense, Protein folding and degradation, Protein homeostasis maintenance, Proteome, Satellite cells, Skeletal muscle
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Identifikatorer
URN: urn:nbn:se:kth:diva-140801DOI: 10.1016/j.trprot.2013.12.002Scopus ID: 2-s2.0-84891913289OAI: oai:DiVA.org:kth-140801DiVA, id: diva2:693233
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QC 20140204

Tilgjengelig fra: 2014-02-04 Laget: 2014-01-31 Sist oppdatert: 2014-02-04bibliografisk kontrollert

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