Acute environmental hypoxia induces LC3 lipidation in a genotype‐dependent manner. Issue 2 (7th November 2013)

• Record Type: Journal Article
• Authors: Masschelein, Evi; Van Thienen, Ruud; D'Hulst, Gommaar; Hespel, Peter; Thomis, Martine; Deldicque, Louise
• Is Part Of: FASEB journal. Volume 28:Issue 2(2014)
• Page Start: 1022
• Page End: 1034
• Publication Date: 2013-11-07
• Subjects: exercise -- p62 -- autophagy -- monozygotic twin design; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.13-239863
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract : Hypoxia‐induced muscle wasting is a phenomenon often described with prolonged stays at high altitude, which has been attributed to altered protein metabolism. We hypothesized that acute normobaric hypoxia would induce a negative net protein balance by repressing anabolic and activating proteolytic signaling pathways at rest and postexercise and that those changes could be partially genetically determined. Eleven monozygotic twins participated in an experimental trial in normoxia and hypoxia (10.7% O2 ). Muscle biopsy samples were obtained before and after a 20‐min moderate cycling exercise. In hypoxia at rest, autophagic flux was increased, as indicated by an increased microtubule‐associated protein 1 light chain 3 type II/I (LC3‐II/I) ratio (+25%) and LC3‐II expression (+60%) and decreased p62/SQSTM1 expression (–25%; P <0.05), whereas exercise reversed those changes to a level similar to that with normoxia except for p62/SQSTM1, which was further decreased ( P <0.05). Hypoxia also increased Bnip3 (+34%) and MAFbx (+18%) mRNA levels as well as REDD1 expression (+439%) and AMP‐activated protein kinase phosphorylation (+22%; P <0.05). Among the molecular responses to hypoxia and/or exercise, high monozygotic similarity was found for REDD1, LC3‐II, and LC3‐II/I ( P <0.05). Our results indicate that environmental hypoxia modulates protein metabolism at rest and after moderate exercise by primarily increasing markers of protein breakdown and, more specifically, markers of the autophagy‐lysosomal system, with a modest genetic contribution.—Masschelein, E., Van Thienen, R., D'Hulst, G., Hespel, P., Thomis, M., Deldicque, L. Acute environmental hypoxia induces LC3 lipidation in a genotype‐dependent manner. FASEB J. 28, 1022–1034 (2014). www.fasebj.org