SARS-CoV-2 spike spurs intestinal inflammation via VEGF production in enterocytes.
Fa-Min ZengYing-Wen LiZhao-Hua DengJian-Zhong HeWei LiLijie WangTing LyuZhanyu LiChaoming MeiMeiling YangYingying DongGuan-Min JiangXiaofeng LiXi HuangFei XiaoYe LiuHong ShanHuanhuan HePublished in: EMBO molecular medicine (2022)
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) can cause gastrointestinal (GI) symptoms that often correlate with the severity of COVID-19. Here, we explored the pathogenesis underlying the intestinal inflammation in COVID-19. Plasma VEGF level was particularly elevated in patients with GI symptoms and significantly correlated with intestinal edema and disease progression. Through an animal model mimicking intestinal inflammation upon stimulation with SARS-CoV-2 spike protein, we further revealed that VEGF was over-produced in the duodenum prior to its ascent in the circulation. Mechanistically, SARS-CoV-2 spike promoted VEGF production through activating the Ras-Raf-MEK-ERK signaling in enterocytes, but not in endothelium, and inducing permeability and inflammation. Blockage of the ERK/VEGF axis was able to rescue vascular permeability and alleviate intestinal inflammation in vivo. These findings provide a mechanistic explanation and therapeutic targets for the GI symptoms of COVID-19.