[Effects of TGF-β1 on the expression and secretion of cytokines induced by Aβ1-42 in hippocampal neuron and microglia co-cultures]

Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2018 May 8;34(5):385-388 395. doi: 10.12047/j.cjap.5668.2018.088.
[Article in Chinese]

Abstract

Objective: To investigate the neuroprotective effects of transforming growth factor beta 1(TGF-β1) on the expression and secretion of cytokines induced by Aβ1-42 in hippocampal neurons and microglial co-cultures.

Methods: Hippocampal neurons and microglia obtained from SD rat were co-cultured. TGF-β1 was applied on day 5 after the neurons and microglia co-cultures were incubated at the concentrations of 5 or 20 ng/ml, Aβ1-42 was added 1 h following TGF-β1 application at a concentration of 5 μmol/L. They were incubated for 72 h and then assessed for further studies. Western blot analyses were employed to examine the expression of inducible nitric oxide synthase (iNOS); Real-time PCR and ELISA were used to detect the mRNA expression and secretion of tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β) and insulin-like growth factor-1 (IGF-1).

Results: In the hippocampal neuron-microglia co-cultures, Aβ1-42 induced upregulation of iNOS, TNF-α and IL-1β, downregulation of IGF-1. TGF-β1 pretreatment ameliorated the pro-inflammatory effects caused by Aβ1-42.

Conclusions: TGF-β1 significantly inhibits the increase in inflammatory cytokines and the decrease in neurotrophic factor which are caused by Aβ1-42-induced microglia activation.

Keywords: Aβ1-42; TGF-β1; cytokines; hippocampal neurons; microglia.

MeSH terms

  • Animals
  • Cells, Cultured
  • Coculture Techniques
  • Cytokines
  • Hippocampus*
  • Microglia*
  • Neurons
  • Rats
  • Rats, Sprague-Dawley
  • Transforming Growth Factor beta1
  • Tumor Necrosis Factor-alpha

Substances

  • Cytokines
  • Transforming Growth Factor beta1
  • Tumor Necrosis Factor-alpha