Exploring the mRNA and Plasma Protein Levels of BDNF, NT4, SIRT1, HSP27, and HSP70 in Multiple Sclerosis Patients and Healthy Controls

Int J Mol Sci. 2023 Nov 10;24(22):16176. doi: 10.3390/ijms242216176.

Abstract

Multiple sclerosis (MS) is a chronic, autoimmune neurodegenerative disease affecting the central nervous system. It is a major cause of non-traumatic neurological disability among young adults in North America and Europe. This study focuses on neuroprotective genes (BDNF, NT4/5, SIRT1, HSP70, and HSP27). Gene expression and protein levels of these markers were compared between MS patients and healthy controls. Blood samples were collected from 42 patients with multiple sclerosis (MS) and 48 control subjects without MS. Quantitative real-time PCR was performed to measure the expression of specific genes. The samples were analyzed in duplicate, and the abundance of mRNA was quantified using the 2-ΔCt method. ELISA assay was used to measure the concentration of specific proteins in the plasma samples. The results show that a 3.5-fold decrease in the gene expression of BDNF corresponds to a 1.5-fold downregulation in the associated plasma protein concentration (p < 0.001). Similar trends were observed with NT-4 (five-fold decrease, slight elevation in protein), SIRT1 (two-fold decrease, two-fold protein decrease), HSP70 (four-fold increase, nearly two-fold protein increase), and HSP27 (four-fold increase, two-fold protein increase) (p < 0.001). This study reveals strong correlations between gene expression and protein concentration in MS patients, emphasizing the relevance of these neuroprotective markers in the disease.

Keywords: BDNF; ELISA; HSP27; HSP70; NT-4; SIRT1; correlation; gene expression; multiple sclerosis.

MeSH terms

  • Blood Proteins
  • Brain-Derived Neurotrophic Factor / genetics
  • Brain-Derived Neurotrophic Factor / metabolism
  • HSP27 Heat-Shock Proteins
  • HSP70 Heat-Shock Proteins / genetics
  • HSP70 Heat-Shock Proteins / metabolism
  • Humans
  • Multiple Sclerosis* / genetics
  • Multiple Sclerosis* / metabolism
  • Neurodegenerative Diseases*
  • RNA, Messenger / genetics
  • Sirtuin 1 / genetics
  • Young Adult

Substances

  • Brain-Derived Neurotrophic Factor
  • HSP27 Heat-Shock Proteins
  • Sirtuin 1
  • RNA, Messenger
  • HSP70 Heat-Shock Proteins
  • Blood Proteins
  • SIRT1 protein, human