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

Version 2 2024-06-04, 04:58
Version 1 2018-06-11, 12:34
journal contribution
posted on 2024-06-04, 04:58 authored by Alex B Addinsall, Craig WrightCraig Wright, Chris ShawChris Shaw, Natasha McraeNatasha Mcrae, Len ForganLen Forgan, Chia-Heng Weng, Xavier ConlanXavier Conlan, Paul FrancisPaul Francis, Zoe M Smith, Sofianos Andrikopoulos, Nicole Stupka
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.

History

Journal

American journal of physiology-regulatory, integrative and comparative physiology

Volume

315

Pagination

R380-R396

Location

Bethesda, Md.

Open access

  • Yes

ISSN

0363-6119

eISSN

1522-1490

Language

eng

Publication classification

C1 Refereed article in a scholarly journal

Copyright notice

2018, American Physiological Society

Issue

2

Publisher

American Physiological Society

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