Insulin suppresses MPP⁺-induced neurotoxicity by targeting integrins and syndecans in C6 astrocytes

Abstract

Parkinson’s disease (PD) is the second most common neurodegenerative disease in the elderly. In central nervous system, astrocytes regulates neuronal function via the modulation of synaptic transmission and plasticity, secretion of growth factors, uptake of neurotransmitters and regulation of extracellular ion concentrations and metabolic support of neurons. Therefore, C6 astroglial cells have been used to study the in vitro PD model induced by 1-methyl-4-phenyl pyridinium (MPP⁺). In this study, pre-treatment of insulin inhibited MPP⁺-induced cell membrane damages on LDH and NO releases, which also inhibited the iNOS and Cox-2 levels. Insulin also up-regulated the PI3K and p-GSK-3β protein expressions in C6 cells. In addition, MPP⁺ and/or insulin enhanced the autophagy by increasing LC3-I to LC3-II conversion. Furthermore, MPP⁺-induced toxicity diminished the integrin β3, αV, syndecan-1 and -3. Insulin pre-treatment enhanced the phosphorylation of integrin-linked kinase and further induced the integrin and syndecan molecules. These findings suggest that insulin prevents MPP⁺-induced toxicity through activation of PI3K, p-GSK-3β, autophagy, integrins and syndecans pathways in C6 glial cells.

Keywords:

• Autophagy
• GSK-3β
• integrins
• Parkinson’s disease
• syndecans

Disclosure statement

The authors have no conflicts of interest to declare.

Additional information

Funding

This study was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Korean Ministry of Education, Science and Technology (2013R1A1A2006613).