Academic Journal

Exercise increases phosphorylation of the putative mTORC2 activity readout NDRG1 in human skeletal muscle

التفاصيل البيبلوغرافية
العنوان: Exercise increases phosphorylation of the putative mTORC2 activity readout NDRG1 in human skeletal muscle
المؤلفون: Knudsen, Jonas Roland, Persson, Kaspar Wredstrøm, Meister, Jaroslawna, Carl, Christian Strini, Raun, Steffen Henning, Andersen, Nicoline Resen, Sylow, Lykke, Kiens, Bente, Jensen, Thomas Elbenhardt, Richter, Erik A., Kleinert, Maximilian
المصدر: Knudsen , J R , Persson , K W , Meister , J , Carl , C S , Raun , S H , Andersen , N R , Sylow , L , Kiens , B , Jensen , T E , Richter , E A & Kleinert , M 2022 , ' Exercise increases phosphorylation of the putative mTORC2 activity readout NDRG1 in human skeletal muscle ' , American Journal of Physiology: Endocrinology and Metabolism , vol. 322 , no. 1 , pp. E63-E73 . https://doi.org/10.1152/ajpendo.00389.2021
سنة النشر: 2022
المجموعة: University of Copenhagen: Research / Forskning ved Københavns Universitet
مصطلحات موضوعية: /dk/atira/pure/core/keywords/TheFacultyOfScience, Faculty of Science, Exercise, mTORC2, Skeletal muscle, β-adrenergic signaling, Humans
الوصف: In mice, exercise is suggested to activate the mechanistic target of rapamycin complex 2 (mTORC2) in skeletal muscle, and mTORC2 is required for normal muscle glucose uptake during exercise. Whether this translates to human skeletal muscle and what signaling pathways facilitate the exercise-induced mTORC2 activation is unknown but important to determine given the important role of mTORC2 in metabolism. We herein tested the hypothesis that exercise increases mTORC2 activity in human skeletal muscle and investigated if β 2 -adrenergic receptor (AR) activation mediates exercise-induced mTORC2 activation. We examined several mTORC2 activity readouts (p-NDRG1 Thr346, p-Akt Ser473, p-mTOR S2481, and p-Akt Thr450) in human skeletal muscle biopsies after uphill walking or cycling exercise. In mouse muscles, we assessed mTORC2 activity readouts following acute activation of muscle β 2 -adrenergic or G s signaling and during in vivo and ex vivo muscle contractions. Exercise increased phosphorylation of NDRG1 Thr346 in human soleus, gastrocnemius, and vastus lateralis muscle, without changing p-Akt Ser473, p-Akt Thr450, and p-mTOR Ser2481. In mouse muscle, stimulation of β 2 -adrenergic or G s signaling and ex vivo contractions failed to increase p-NDRG1 Thr346, while in vivo contractions were sufficient to induce p-NDRG1 Thr346. In conclusion, the mTORC2 activity readout p-NDRG1 Thr346 is a novel exercise-responsive signaling protein in human skeletal muscle. Notably, contraction-induced p-NDRG1 Thr346 appears to require a systemic factor. Unlike exercise, and in contrast to published data obtained in cultured muscles cells, stimulation of β 2 -adrenergic signaling is not sufficient to trigger NDRG1 phosphorylation in mature mouse skeletal muscle.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
DOI: 10.1152/ajpendo.00389.2021
الاتاحة: https://curis.ku.dk/portal/da/publications/exercise-increases-phosphorylation-of-the-putative-mtorc2-activity-readout-ndrg1-in-human-skeletal-muscle(9fe94f71-1070-4f6c-941a-d61eb56d46b7).html
https://doi.org/10.1152/ajpendo.00389.2021
https://curis.ku.dk/ws/files/286421704/Knudsen_et_al_American_Journal_of_Physiology_Endocrinology_and_Metabolism_2021_00389_Accepted_manuscript_.pdf
Rights: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.8CA805F7
قاعدة البيانات: BASE
الوصف
DOI:10.1152/ajpendo.00389.2021