分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

The effect of 4.3 GHz high-power microwave exposure on human corneal epithelial cells

Anning Gao, Xuelong Zhao, Shuang Wu, Xiaoman Liu, Xinyu Wang, Luhao Tan, Zhihui Li, Guofu Dong, Changzhen Wang

Journal:Frontiers in Cell and Developmental Biology

IF:4.3

DOI:10.3389/fcell.2026.1729198

PMID:

Published:2026-01-22

research field:分子生物学真菌遗传学微生物学植物病理学

Abstract

Introduction: High-power microwave (HPM) exposure can produce biological effects in cells, but the specific characteristics and mechanisms of these effects in ocular tissues remain poorly defined. This study aimed to investigate the biological responses of human corneal epithelial cells (HCE-T) to 4.3 GHz HPM exposure, with a focus on moderate-dose effects.Methods: HCE-T cells were exposed to 4.3 GHz HPM at average specific absorption rates (SARs) of 1.64, 3.28, and 8.2 W/kg. Cellular responses were evaluated by measuring cell viability, reactive oxygen species (ROS) generation, mitochondrial membrane potential, and apoptosis at multiple time points. Transcriptomic analysis was performed to identify underlying molecular pathways.Results: Moderate-dose exposure (3.28 W/kg) resulted in the most pronounced cellular effects, including early and significant ROS elevation, marked collapse of mitochondrial membrane potential, the highest apoptosis rate, and sustained inhibition of proliferation. Transcriptomic profiling showed strong suppression of the mTOR signaling pathway, upregulation of TSC2, and activation of Polycomb-mediated chromatin remodeling, suggestive of autophagy induction and irreversible cell cycle arrest. In contrast, low-dose exposure (1.64 W/kg) primarily activated DNA repair and adaptive pathways, while high-dose exposure (8.2 W/kg) predominantly disrupted metabolic and membrane signaling with a trend toward recovery.Discussion: These findings demonstrate that moderate-dose 4.3 GHz HPM exposure induces a uniquely strong stress response in HCE-T cells, characterized by oxidative stress, mitochondrial dysfunction, and activation of stress-related signaling pathways. These results highlight the importance of considering specific exposure conditions in assessing HPM bioeffects and ocular safety.

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