Deficiency of selenoprotein S, an endoplasmic reticulum resident oxidoreductase, impairs the contractile function of fast-twitch hindlimb muscles

• Published in: American journal of physiology. Regulatory, integrative and comparative physiology Vol. 315; no. 2; pp. R380 - R396
• Main Authors: Addinsall, Alex B, Wright, Craig R, Shaw, Chris S, McRae, Natasha L, Forgan, Leonard G, Weng, Chia-Heng, Conlan, Xavier A, Francis, Paul S, Smith, Zoe M, Andrikopoulos, Sofianos, Stupka, Nicole
• Format: Journal Article
• Language: English
• Published: United States American Physiological Society 01.08.2018
• Subjects: Abundance; Adult; Animals; Antioxidants; Body Composition; Carrier Proteins - genetics; Carrier Proteins - metabolism; Cellular stress response; Clonal deletion; Contractility; Electric Stimulation; Endoplasmic reticulum; Endoplasmic Reticulum - enzymology; Endoplasmic Reticulum Stress; Gene expression; Genotypes; Hindlimb; Humans; Inflammation; Localization; Male; Membrane Glycoproteins - genetics; Membrane Glycoproteins - metabolism; Membrane Proteins - deficiency; Membrane Proteins - genetics; Membrane Proteins - metabolism; Metabolism; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, Knockout; MicroRNAs; Motor Activity; Muscle Contraction; Muscle Fibers, Fast-Twitch - enzymology; Muscle Fibers, Slow-Twitch - enzymology; Muscle Strength; Muscles; Oxidoreductase; Physical activity; Proteins; Selenoproteins - deficiency; Selenoproteins - genetics; Selenoproteins - metabolism; Stimulation; Stress; Stresses; Thioredoxin; Thioredoxins - genetics; Thioredoxins - metabolism; Transcription; Transcription Factor CHOP - genetics; Transcription Factor CHOP - metabolism; Young Adult; selenoprotein S; thioredoxin; SEPS1; endoplasmic reticulum stress; fast-twitch muscle
• ISSN: 0363-6119; 1522-1490
• DOI: 10.1152/ajpregu.00244.2017

Selenoprotein S (Seps1) is an endoplasmic reticulum (ER) resident antioxidant implicated in ER stress and inflammation. In human vastus lateralis and mouse hindlimb muscles, Seps1 localization and expression were fiber-type specific. In male Seps1 heterozygous mice, spontaneous physical activity was reduced compared with wild-type littermates ( d = 1.10, P = 0.029). A similar trend was also observed in Seps1 knockout mice ( d = 1.12, P = 0.051). Whole body metabolism, body composition, extensor digitorum longus (EDL), and soleus mass and myofiber diameter were unaffected by genotype. However, in isolated fast EDL muscles from Seps1 knockout mice, the force frequency curve (FFC; 1-120 Hz) was shifted downward versus EDL muscles from wild-type littermates ( d = 0.55, P = 0.002), suggestive of reduced strength. During 4 min of intermittent, submaximal (60 Hz) stimulation, the genetic deletion or reduction of Seps1 decreased EDL force production ( d = 0.52, P < 0.001). Furthermore, at the start of the intermittent stimulation protocol, when compared with the 60-Hz stimulation of the FFC, EDL muscles from Seps1 knockout or Seps1 heterozygous mice produced 10% less force than those from wild-type littermates ( d = 0.31, P < 0.001 and d = 0.39, P = 0.015). This functional impairment was associated with reduced mRNA transcript abundance of thioredoxin-1 ( Trx1), thioredoxin interacting protein ( Txnip), and the ER stress markers Chop and Grp94, whereas, in slow soleus muscles, Seps1 deletion did not compromise contractile function and Trx1 ( d = 1.38, P = 0.012) and Txnip ( d = 1.27, P = 0.025) gene expression was increased. Seps1 is a novel regulator of contractile function and cellular stress responses in fast-twitch muscles.