STIM1 R304W causes muscle degeneration and impaired platelet activation in mice

Cell Calcium. 2018 Dec:76:87-100. doi: 10.1016/j.ceca.2018.10.001. Epub 2018 Oct 5.

Abstract

STIM1 and ORAI1 regulate store-operated Ca2+ entry (SOCE) in most cell types, and mutations in these proteins have deleterious and diverse effects. We established a mouse line expressing the STIM1 R304 W gain-of-function mutation causing Stormorken syndrome to explore effects on organ and cell physiology. While STIM1 R304 W was lethal in the homozygous state, surviving mice presented with reduced growth, skeletal muscle degeneration, and reduced exercise endurance. Variable STIM1 expression levels between tissues directly impacted cellular SOCE capacity. In contrast to patients with Stormorken syndrome, STIM1 was downregulated in fibroblasts from Stim1R304W/R304W mice, which maintained SOCE despite constitutive protein activity. In studies using foetal liver chimeras, STIM1 protein was undetectable in homozygous megakaryocytes and platelets, resulting in impaired platelet activation and absent SOCE. These data indicate that downregulation of STIM1 R304 W effectively opposes the gain-of-function phenotype associated with this mutation, and highlight the importance of STIM1 in skeletal muscle development and integrity.

Keywords: Muscle degeneration; Platelet dysfunction; Stim1 R304W; Stim1 expression; Stormorken syndrome.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism
  • Female
  • Locomotion
  • Male
  • Mice
  • Mice, Inbred Strains
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / pathology*
  • Platelet Activation*
  • Stromal Interaction Molecule 1 / metabolism*

Substances

  • Stim1 protein, mouse
  • Stromal Interaction Molecule 1
  • Calcium