کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8318771 | 1539113 | 2018 | 7 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Strategies of biochemical adaptation for hibernation in a South American marsupial, Dromiciops gliroides: 2. Control of the Akt pathway and protein translation machinery
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کلمات کلیدی
4EBPeIF4EEukaryotic translation initiation factorseukaryotic translation initiation factor 2AmTORGSK-3βp70S6KeIF2αIGF-1RTSC2eukaryotic translation initiation factor 4E - 4e عامل آغازگر ترجمه یوکاریوتیAkt - آکتTOP - بالاHibernation - خواب زمستانی، زمستانخوابیBrain - مغزMechanistic target of rapamycin - هدف مکانیکی رپامایسینribosomal protein S6 kinase - پروتئین ریبوزومی S6 کینازprotein kinase B - پروتئین کیناز Btuberous sclerosis complex 2 - پیچیده سلولهای توبولی 2Liver - کبدKidney - کلیهglycogen synthase kinase 3 beta - گلیکوزین سنتاز کیناز 3 بتاinsulin-like growth factor 1 receptor - گیرنده فاکتور رشد 1 مانند انسولین
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
زیست شیمی
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چکیده انگلیسی
When faced with harsh environmental conditions, the South American marsupial, monito del monte (Dromiciops gliroides), reduces its body temperature and uses either daily torpor or multiday hibernation to survive. This study used ELISA and multiplex assays to characterize the responses to hibernation by three regulatory components of protein translation machinery [p-eIF2α(S51), p-eIF4E(S209), p-4EBP(Thr37/46)] and eight targets involved in upstream signaling control of translation [p-IGF-1R(Tyr1135/1136), PTEN(S380), p-Akt(S473), p-GSK-3α(S21), p-GSK-3β(S9), p-TSC2(S939), p-mTOR(S2448), and p70S6K(T412)]. Liver, brain and kidney were analyzed comparing control and hibernation (4 days continuous torpor) conditions. In the liver, increased phosphorylation of IGF-1R, Akt, GSK-3β, TSC2, mTOR, eIF2α, and 4EBP (1.60-1.98 fold compared to control) occurred during torpor suggesting that the regulatory phosphorylation cascade and protein synthesis remained active during torpor. However, responses by brain and kidney differed; torpor resulted in increased phosphorylation of GSK-3β (2.15-4.17 fold) and TSC2 (2.03-3.65 fold), but phosphorylated Akt decreased (to 34-62% of control levels). Torpor also led to an increase in phosphorylated eIF2α (1.4 fold) content in the brain. These patterns of differential protein phosphorylation in brain and kidney were indicative of suppression of protein translation but also could suggest an increase in antioxidant and anti-apoptotic signaling during torpor. Previous studies of liver metabolism in hibernating eutherian mammals have shown that Akt kinase and its downstream signaling components play roles in facilitating hypometabolism by suppressing energy expensive anabolic processes during torpor. However, the results in this study reveal differences between eutherian and marsupial hibernators, suggesting alternative actions of liver Akt during torpor.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology - Volume 224, October 2018, Pages 19-25
Journal: Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology - Volume 224, October 2018, Pages 19-25
نویسندگان
Bryan E. Luu, Sanoji Wijenayake, Jing Zhang, Shannon N. Tessier, Julian F. Quintero-Galvis, Juan Diego Gaitán-Espitia, Roberto F. Nespolo, Kenneth B. Storey,