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SARS-CoV-2 刺突通过肠上皮细胞中 VEGF 的产生引发肠道炎症。

SARS-CoV-2 spike spurs intestinal inflammation via VEGF production in enterocytes.

机构信息

Guangdong Provincial Key Laboratory of Biomedical Imaging and Guangdong Provincial Engineering Research Center of Molecular Imaging, The Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, China.

Department of Pathology, The Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, China.

出版信息

EMBO Mol Med. 2022 May 9;14(5):e14844. doi: 10.15252/emmm.202114844. Epub 2022 Apr 19.

Abstract

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.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)可引起胃肠道(GI)症状,这些症状通常与 COVID-19 的严重程度相关。在这里,我们探讨了 COVID-19 中肠道炎症的发病机制。有胃肠道症状的患者血浆 VEGF 水平特别升高,与肠道水肿和疾病进展显著相关。通过模拟 SARS-CoV-2 刺突蛋白刺激引起的肠道炎症的动物模型,我们进一步发现 VEGF 在其进入循环之前在十二指肠中过度产生。在机制上,SARS-CoV-2 刺突蛋白通过激活肠细胞中的 Ras-Raf-MEK-ERK 信号通路而不是内皮细胞来促进 VEGF 的产生,并诱导通透性和炎症。阻断 ERK/VEGF 轴能够挽救血管通透性并减轻体内肠道炎症。这些发现为 COVID-19 的胃肠道症状提供了机制解释和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ee/9081906/79df0df66ef8/EMMM-14-e14844-g001.jpg

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