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A longitudinal molecular and cellular lung atlas of lethal SARS-CoV-2 infection in K18-hACE2 transgenic mice

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dc.contributor.author권호근-
dc.contributor.author김성희-
dc.contributor.author남기택-
dc.contributor.author서준영-
dc.contributor.author신전수-
dc.contributor.author윤종휘-
dc.date.accessioned2024-03-22T07:16:30Z-
dc.date.available2024-03-22T07:16:30Z-
dc.date.issued2024-01-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/198720-
dc.description.abstractBackground The global pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has led to approximately 500 million cases and 6 million deaths worldwide. Previous investigations into the pathophysiology of SARS-CoV-2 primarily focused on peripheral blood mononuclear cells from patients, lacking detailed mechanistic insights into the virus's impact on inflamed tissue. Existing animal models, such as hamster and ferret, do not faithfully replicate the severe SARS-CoV-2 infection seen in patients, underscoring the need for more relevant animal system-based research. Methods In this study, we employed single-cell RNA sequencing (scRNA-seq) with lung tissues from K18-hACE2 transgenic (TG) mice during SARS-CoV-2 infection. This approach allowed for a comprehensive examination of the molecular and cellular responses to the virus in lung tissue. Findings Upon SARS-CoV-2 infection, K18-hACE2 TG mice exhibited severe lung pathologies, including acute pneumonia, alveolar collapse, and immune cell infiltration. Through scRNA-seq, we identified 36 different types of cells dynamically orchestrating SARS-CoV-2-induced pathologies. Notably, SPP1(+) macrophages in the myeloid compartment emerged as key drivers of severe lung inflammation and fibrosis in K18-hACE2 TG mice. Dynamic receptor-ligand interactions, involving various cell types such as immunological and bronchial cells, defined an enhanced TGF beta signaling pathway linked to delayed tissue regeneration, severe lung injury, and fibrotic processes. Interpretation Our study provides a comprehensive understanding of SARS-CoV-2 pathogenesis in lung tissue, surpassing previous limitations in investigating inflamed tissues. The identified SPP1+ macrophages and the dysregulated TGF beta signaling pathway offer potential targets for therapeutic intervention. Insights from this research may contribute to the development of innovative diagnostics and therapies for COVID-19.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherElsevier-
dc.relation.isPartOfEBIOMEDICINE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAnimals-
dc.subject.MESHBronchi-
dc.subject.MESHCOVID-19*-
dc.subject.MESHCricetinae-
dc.subject.MESHDisease Models, Animal-
dc.subject.MESHFerrets-
dc.subject.MESHHumans-
dc.subject.MESHLeukocytes, Mononuclear-
dc.subject.MESHLung-
dc.subject.MESHMelphalan*-
dc.subject.MESHMice-
dc.subject.MESHMice, Transgenic-
dc.subject.MESHSARS-CoV-2-
dc.subject.MESHTransforming Growth Factor beta-
dc.subject.MESHgamma-Globulins*-
dc.titleA longitudinal molecular and cellular lung atlas of lethal SARS-CoV-2 infection in K18-hACE2 transgenic mice-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Microbiology (미생물학교실)-
dc.contributor.googleauthorSeunghoon Choi-
dc.contributor.googleauthorJusung Lee-
dc.contributor.googleauthorSuhyeon Kim-
dc.contributor.googleauthorYoun Woo Lee-
dc.contributor.googleauthorGi-Cheon Kim-
dc.contributor.googleauthorSeung-Min Hong-
dc.contributor.googleauthorSe-Hee An-
dc.contributor.googleauthorHyuna Noh-
dc.contributor.googleauthorKyung Eun Kim-
dc.contributor.googleauthorDain On-
dc.contributor.googleauthorSang Gyu Lee-
dc.contributor.googleauthorHui Jeong Jang-
dc.contributor.googleauthorSung-Hee Kim-
dc.contributor.googleauthorJiseon Kim-
dc.contributor.googleauthorJung Seon Seo-
dc.contributor.googleauthorJeong Jin Kim-
dc.contributor.googleauthorIn Ho Park-
dc.contributor.googleauthorJooyeon Oh-
dc.contributor.googleauthorDa-Jung Kim-
dc.contributor.googleauthorJong-Hwi Yoon-
dc.contributor.googleauthorSang-Hyuk Seok-
dc.contributor.googleauthorYu Jin Lee-
dc.contributor.googleauthorSeo Yeon Kim-
dc.contributor.googleauthorYoung Been Kim-
dc.contributor.googleauthorJi-Yeon Hwang-
dc.contributor.googleauthorHyo-Jung Lee-
dc.contributor.googleauthorHong Bin Kim-
dc.contributor.googleauthorJun Won Park-
dc.contributor.googleauthorJun-Won Yun-
dc.contributor.googleauthorJeon-Soo Shin-
dc.contributor.googleauthorJun-Young Seo-
dc.contributor.googleauthorKi Taek Nam-
dc.contributor.googleauthorKang-Seuk Choi-
dc.contributor.googleauthorHo-Keun Kwon-
dc.contributor.googleauthorHo-Young Lee-
dc.contributor.googleauthorJong Kyoung Kim-
dc.contributor.googleauthorJe Kyung Seong-
dc.identifier.doi10.1016/j.ebiom.2023.104932-
dc.contributor.localIdA05782-
dc.contributor.localIdA06017-
dc.contributor.localIdA01243-
dc.contributor.localIdA01911-
dc.contributor.localIdA02144-
dc.relation.journalcodeJ03279-
dc.identifier.eissn2352-3964-
dc.identifier.pmid38118400-
dc.subject.keywordK18-hACE2 TG mice-
dc.subject.keywordLung inflammation-
dc.subject.keywordSARS-CoV-2 infection-
dc.subject.keywordSPP1-
dc.subject.keywordTGFβ-
dc.subject.keywordscRNA-seq-
dc.contributor.alternativeNameKwon, Ho-Keun-
dc.contributor.affiliatedAuthor권호근-
dc.contributor.affiliatedAuthor김성희-
dc.contributor.affiliatedAuthor남기택-
dc.contributor.affiliatedAuthor서준영-
dc.contributor.affiliatedAuthor신전수-
dc.citation.volume99-
dc.citation.startPage104932-
dc.identifier.bibliographicCitationEBIOMEDICINE, Vol.99 : 104932, 2024-01-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Microbiology (미생물학교실) > 1. Journal Papers

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