Association between SGK1 and α-synuclein in skeletal muscle in an MPTP-induced Parkinson's disease model

Neurosci Lett. 2023 Sep 25:814:137464. doi: 10.1016/j.neulet.2023.137464. Epub 2023 Aug 25.

Abstract

Parkinson's disease (PD) is a neurodegenerative disease caused by loss of dopaminergic neurons in the substantia nigra and it is known to involve the accumulation of α-synuclein (α-syn), which is a neuroprotein that promotes degeneration of dopaminergic neurons. Serum/glucocorticoid-related kinase 1 (SGK1) is involved in the physiological and pathological processes in neurons. The aim of this study was to examine the relationship between SGK1 and α-syn expression in muscle tissue of a PD model and in C2C12 cells. Western blotting, immunohistochemistry, and immunofluorescence microscopy confirmed reduced SGK1 and increased α-syn expression in skeletal muscle of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-treated mice compared to the control group. To determine the relationship between SGK1 and α-syn, SGK1 small interfering RNA (siRNA) knockdown was performed in C2C12 cells, which showed that suppression of SGK1 levels resulted in increased α-syn expression. The main finding of our study is that reduction of SGK1 expression contributes to the pathogenesis of PD by increasing the expression of α-syn in skeletal muscle of MPTP-treated mice and C2C12 cells. This study confirms that decreased SGK1 induces increased α-syn expression in skeletal muscle, which suggests that maintaining SGK1 expression may improve PD symptoms.

Keywords: C2C12 cell; MPTP; Parkinson's disease; SGK1; Skeletal muscle; α-synuclein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine / pharmacology
  • Animals
  • Disease Models, Animal
  • Dopaminergic Neurons / metabolism
  • Glucocorticoids / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Muscle, Skeletal / metabolism
  • Neurodegenerative Diseases* / metabolism
  • Parkinson Disease* / metabolism
  • Substantia Nigra / metabolism
  • alpha-Synuclein / metabolism

Substances

  • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
  • alpha-Synuclein
  • Glucocorticoids
  • serum-glucocorticoid regulated kinase
  • Snca protein, mouse