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The potential involvement of JAK-STAT signaling pathway in the COVID-19 infection assisted by ACE2.
Luo, Jing; Lu, Saisai; Yu, Mengjiao; Zhu, Lixia; Zhu, Chengwei; Li, Chenlu; Fang, Jinxia; Zhu, Xiaochun; Wang, Xiaobing.
  • Luo J; Rheumatology Department, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Lu S; Rheumatology Department, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Yu M; Rheumatology Department, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Zhu L; Rheumatology Department, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Zhu C; Rheumatology Department, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Li C; Rheumatology Department, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Fang J; Rheumatology Department, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Zhu X; Rheumatology Department, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Wang X; Rheumatology Department, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China. Electronic address: gale820907@163.com.
Gene ; 768: 145325, 2021 Feb 05.
Article in English | MEDLINE | ID: covidwho-947226
ABSTRACT
COVID-19, a novel identified coronavirus disease due to Severe Acute Respiratory Syndrome coronaviruses 2 (SARS-Cov-2) infection, has posed a significant threat to public health worldwide. It has been reported COVID-19 keeps substantial nucleotide similarity and shares common receptor, Angiotensin-converting enzyme 2 (ACE2) with Severe Acute Respiratory Syndrome coronaviruses (SARS-Cov). Here, we investigated the gene expression of ACE2 and identified associated pathways of SARS-Cov as a useful reference for a deepening understanding of COVID-19. The results indicated the ACE2 was overexpressed in human airway epithelial cells (HAEs), especially at 72 h after SARS-Cov infection. We found ACE2 might regulate immune response through immunological activation-associated pathways in the process of in both SARS-Cov and SARS-Cov-2 infection, where the activation of B cells, macrophages, helper T cells 1 (Th1 cells) and the inhibition of Foxp3 + regulatory T (Treg) cells and CD8 + T cells were found to be prominent. Finally, significant correlation between ACE2 and JAK-STAT signaling pathway was identified which indicate that JAK-STAT signaling pathway might involve in the downstream action of the overactivation of ACE2. These findings are expected to gain a further insight into the action mechanism of COVID-19 infection and provide a promising target for designing effective therapeutic strategies.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: STAT Transcription Factors / Janus Kinases / Angiotensin-Converting Enzyme 2 / COVID-19 Type of study: Observational study Limits: Humans Language: English Journal: Gene Year: 2021 Document Type: Article Affiliation country: J.gene.2020.145325

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Full text: Available Collection: International databases Database: MEDLINE Main subject: STAT Transcription Factors / Janus Kinases / Angiotensin-Converting Enzyme 2 / COVID-19 Type of study: Observational study Limits: Humans Language: English Journal: Gene Year: 2021 Document Type: Article Affiliation country: J.gene.2020.145325