[Relationship between activation of microglia and Jaks phosphorylation induced by microwave irradiation]

Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2010 Jun;28(6):401-4.
[Article in Chinese]

Abstract

Objective: To explore the relationship between microglial proinflammatory and electromagnetic radiation and unveil the role of microglia in microwave radiation induced central nervous system injury.

Methods: N9 microglia cells cultured in vitro were exposed to microwave at 90 mW/cm2. Cell flow cytometry was used to observe the expression of CD11b at different time points after exposure; ELISA was used to detect the concentration of TNF-alpha in N9 cell culture supernatant; RT-PCR analysis confirmed iNOS mRNA expression in N9 microglia cells; and Nitrate Reductase Method was used to test NO amount in culture supernatant.

Results: The CD11b positive microglial cells increased significantly at 3 h after microwave exposure (P < 0.05), continued to increase until 24 h and peaked at 6 h after exposure. The amount of TNF-alpha rose dramatically from 1 h to 24 h after exposure (P < 0.01) and peaked at 3 h [(762.1 +/- 61.5) pg/ml] after exposure (P < 0.01). The level of NO started to increase at 1 h [(4.48-0.59) micromol/L] and lasted for 24 h after exposure. The expression of iNOS mRNA increased significantly at 1 h (P < 0.05), and tripled the original expression at 6 h after exposure, hereafter, it decreased slightly, but all were higher than the control group within 24 h after exposure.

Conclusion: Microwave radiation could induce the activation of microglia cells. The activated microglia cells could induce microglial proinflammatory by producing large amounts of TNF-alpha, NO, etc.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cells, Cultured
  • Mice
  • Microglia / metabolism*
  • Microglia / radiation effects*
  • Microwaves*
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase / metabolism
  • Phosphorylation
  • RNA, Messenger / genetics
  • Tumor Necrosis Factors / metabolism

Substances

  • RNA, Messenger
  • Tumor Necrosis Factors
  • Nitric Oxide
  • Nitric Oxide Synthase