Abstract

Insulin-like growth factor 2 (IGF2) and autophagy-related genes have been proposed as biomolecules of interest related to idiopathic Parkinson’s disease (PD). The objective of this study was to determine the IGF2 and IGF1 levels in plasma and peripheral blood mononuclear cells (PBMCs) from patients with moderately advanced PD and explore the potential correlation with autophagy-related genes in the same blood samples. IGF1 and IGF2 levels in patients' plasma were measured by ELISA, and the IGF2 expression levels were determined by real-time PCR and Western blot in PBMCs. The expression of autophagy-related genes was evaluated by real-time PCR. The results show a significant decrease in IGF2 plasma levels in PD patients compared with a healthy control group. We also report a dramatic decrease in IGF2 mRNA and protein levels in PBMCs from PD patients. In addition, we observed a downregulation of key components of the initial stages of the autophagy process. Although IGF2 levels were not directly correlated with disease severity, we found a correlation between its levels and autophagy gene profile expression in a sex-dependent pattern from the same samples. To further explore this correlation, we treated mice macrophages cell culture with α-synuclein and IGF2. While α-synuclein treatment decreased levels Atg5, IGF2 treatment reverted these effects, increasing Atg5 and Beclin1 levels. Our results suggest a relationship between IGF2 levels and the autophagy process in PD and their potential application as multi-biomarkers to determine PD patients' stages of the disease.

Highlights

  • Insulin-like growth factor 2 (IGF2) and autophagy-related genes have been proposed as biomolecules of interest related to idiopathic Parkinson’s disease (PD)

  • We found a decrease in ATG5, ULK1, and BECLIN1 transcriptional levels in peripheral blood mononuclear cells (PBMCs) samples from sporadic PD patients, associated with the reduction of IGF2 mRNA and protein levels

  • Since IGF2 is a soluble secreted factor, we measured IGF2 in plasma from PD patients using ELISA. This analysis revealed a slight but significant decrease in circulating IGF2 present in the plasma samples derived from PD patients compared to control subjects (p = 0.0185, Fig. 1A), which may be related to the different contributions of tissues and cell types to plasmatic IGF2 levels

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Summary

Introduction

Insulin-like growth factor 2 (IGF2) and autophagy-related genes have been proposed as biomolecules of interest related to idiopathic Parkinson’s disease (PD). The objective of this study was to determine the IGF2 and IGF1 levels in plasma and peripheral blood mononuclear cells (PBMCs) from patients with moderately advanced PD and explore the potential correlation with autophagy-related genes in the same blood samples. IGF2 showed a substantial expression reduction in peripheral blood mononuclear cells (PBMCs) and brain tissues from HD patients, arising as an interesting biomarker for neurodegenerative diseases. A single-nucleotide polymorphism (SNP) in the IGF2 gene was identified as a potential modifier of the susceptibility to develop idiopathic PD in a Caucasian group from ­Australia[46] This polymorphism was associated with reduced IGF2 expression levels, lower body weight, and low levels of tyrosine hydroxylase enzyme (TH) expression, the limiting enzyme in dopamine ­production[47]. The molecular mechanism involved in IGF2 neuroprotection is still under study

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