Exosomal circEZH2_005, an intestinal injury biomarker, alleviates intestinal ischemia/reperfusion injury by mediating Gprc5a signaling

作者：Zhang, Wenjuan; Zhou, Bowei; Yang, Xiao; Zhao, Jin; Hu, Jingjuan; Ding, Yuqi; Zhan, Shuteng; Yang, Yifeng; Chen, Jun; Zhang, Fu; Zhao, Bingcheng; Deng, Fan; Lin, Zebin; Sun, Qishun; Zhang, Fangling; Yao, Zhiwen; Liu, Weifeng; Li, Cai^*; Liu, Ke-Xuan^*

来源：Nature Communications, 2023, 14(1): 5437.

DOI：10.1038/s41467-023-41147-3

• NUCLEAR RIBONUCLEOPROTEIN A1
• EXTRACELLULAR VESICLES
• CIRCULAR RNA
• BINDING
• CANCER
• REGENERATION
• PROTEIN
• ROLES
• MICE

Intestinal ischemia/reperfusion (I/R) injury is a severe clinical condition without optimal diagnostic markers nor clear molecular etiological insights. Plasma exosomal circular RNAs (circRNAs) are valuable biomarkers and therapeutic targets for various diseases, but their role in intestinal I/R injury remains unknown. Here we screen the expression profile of circRNAs in intestinal tissue exosomes collected from intestinal I/R mice and identify circEZH2_005 as a significantly downregulated exosomal circRNA. In parallel, circEZH2_005 is also reduced in the plasma of clinical cardiac surgery patients who developed postoperative intestinal I/R injury. Exosomal circEZH2_005 displays a significant diagnostic value for intestinal injury induced by I/R. Mechanistically, circEZH2_005 is highly expressed in intestinal crypt cells. CircEZH2_005 upregulation promotes the proliferation of Lgr5+ stem cells by direct interaction with hnRNPA1, and enhanced Gprc5a stability, thereby alleviating I/R-induced intestinal mucosal damage. Hence, exosomal circEZH2_005 may serve as a biomarker for intestinal I/R injury and targeting the circEZH2_005/hnRNPA1/Gprc5a axis may be a potential therapeutic strategy for intestinal I/R injury. @@@ Currently, intestinal ischemia/reperfusion injury lacks ideal diagnostic markers and effective therapeutic targets. Here, the authors show exosomal circEZH2_005 is an intestinal injury biomarker and protects the intestine from ischemia/reperfusion injury by promoting crypt cell proliferation via affecting hnRNPA1- mediated Gprc5a stability.

• 单位
  南方医科大学