Extra-nuclear telomerase reverse transcriptase (TERT) regulates glucose transport in skeletal muscle cells

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

卷:1842

Article

Shaheen, Fozia¹  Grammatopoulos, Dimitris K.¹  Mueller, Juergen¹  Zammit, Victor A.¹  Lehnert, Hendrik^1,2 

[1] Univ Warwick, Clin Sci Res Labs, Warwick Med Sch, Div Metab & Vasc Hlth, Warwick CV2 2DX, England

[2] Univ Hosp Schleswig Holstein, Dept Med 1, D-23538 Lubeck, Germany

关键词: TERT;    Glucose transporter;    Insulin;    Ageing;    Diabetes;    Muscle;   

DOI  :  10.1016/j.bbadis.2014.06.018

来源: Elsevier

【 摘 要 】

Telomerase reverse transcriptase (TERT) is a key component of the telomerase complex. By lengthening telomeres in DNA strands, TERT increases senescent cell lifespan. Mice that lack TERT age much faster and exhibit age-related conditions such as osteoporosis, diabetes and neurodegeneration. Accelerated telomere shortening in both human and animal models has been documented in conditions associated with insulin resistance, including T2DM. We investigated the role of TERT, in regulating cellular glucose utilisation by using the myoblastoma cell line C2C12, as well as primary mouse and human skeletal muscle cells. Inhibition of TERT expression or activity by using siRNA (100 nM) or specific inhibitors (100 nM) reduced basal 2-deoxyglucose uptake by similar to 50%, in all cell types, without altering insulin responsiveness. In contrast, TERT over-expression increased glucose uptake by 325-fold. In C2C12 cells TEAT protein was mostly localised intracellularly and stimulation of cells with insulin induced translocation to the plasma membrane. Furthermore, co-immunoprecipitation experiments in C2C12 cells showed that TERT was constitutively associated with glucose transporters (GLUTs) 1,4 and 12 via an insulin insensitive interaction that also did not require intact PI3-K and mTOR pathways. Collectively, these findings identified a novel extra-nuclear function of TERT that regulates an insulin-insensitive pathway involved in glucose uptake in human and mouse skeletal muscle cells. (C) 2014 Elsevier B.V. All rights reserved.

【 授权许可】

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