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肺组织中 miR-203a-3p 的下调可增强血管内皮生长因子/Notch 信号通路对高原低氧的反应。

Downregulation of lung miR-203a-3p expression by high-altitude hypoxia enhances VEGF/Notch signaling.

机构信息

School of Disaster Medical Research, Tianjin University, Tianjin 300072, China.

Logistics University of Chinese People's Armed Police Force, Tianjin 300162, China.

出版信息

Aging (Albany NY). 2020 Feb 29;12(5):4247-4267. doi: 10.18632/aging.102878.

Abstract

Hypoxia-related microRNAs (miRNAs) are involved in the pathogenesis of various diseases. Because potential variations in miRNA expression mediated by hypoxic lung injury at high altitude remain incompletely characterized, we used a rat model to investigate the biochemical and miRNA changes induced by high-altitude hypoxia. After 24, 48, or 72 h of hypoxic exposure, expression of VEGF/Notch pathway-related proteins were increased in rat lung tissues. Microarray screening of hypoxic lung samples revealed 57 differentially expressed miRNAs, 19 of which were related to the VEGF/Notch signaling pathway. We verified that the top downregulated miRNA (miR-203a-3p) suppresses VEGF-A translation through direct binding and also indirectly reduces Notch1, VEGFR2, and Hes1 levels, which restricts the angiogenic capacity of pulmonary microvascular endothelial cells in vitro. These findings may aid in the development of new therapeutic strategies for the prevention and treatment of hypoxic lung injury at high altitude.

摘要

缺氧相关 microRNAs(miRNAs)参与各种疾病的发病机制。由于高海拔缺氧引起的 miRNA 表达的潜在变化尚不完全清楚,我们使用大鼠模型来研究高原缺氧引起的生化和 miRNA 变化。缺氧暴露 24、48 或 72 小时后,大鼠肺组织中 VEGF/Notch 通路相关蛋白的表达增加。缺氧肺组织样本的微阵列筛选显示 57 个差异表达的 miRNAs,其中 19 个与 VEGF/Notch 信号通路有关。我们验证了下调最明显的 miRNA(miR-203a-3p)通过直接结合抑制 VEGF-A 的翻译,并且还间接降低 Notch1、VEGFR2 和 Hes1 水平,从而限制体外肺微血管内皮细胞的血管生成能力。这些发现可能有助于开发新的治疗策略,以预防和治疗高原缺氧性肺损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c821/7093161/afea00924b8d/aging-12-102878-g001.jpg

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