4.8 Article

Adult stem cell-derived complete lung organoid models emulate lung disease in COVID-19

期刊

ELIFE
卷 10, 期 -, 页码 -

出版社

eLIFE SCIENCES PUBL LTD
DOI: 10.7554/eLife.66417

关键词

lung organoid; SARS-CoV2; disease modeling; computational; immune response; AT2 differentiation; Human; Viruses

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资金

  1. National Institute of Diabetes and Digestive and Kidney Diseases [1R01DK107585-01A1, 3R01DK107585-05S1]
  2. National Institute of Allergy and Infectious Diseases [R01-AI 155696, R01-AI141630]
  3. National Cancer Institute [CA160911, CA100768]
  4. National Institute of General Medical Sciences [R01-GM138385]
  5. National Heart, Lung, and Blood Institute [R01-HL32225, R01-HL137052]
  6. University of California, San Diego [UCOP-R01RG3780]
  7. Department of Veterans Affairs Merit Award [1I01BX004767]

向作者/读者索取更多资源

A human lung model of COVID-19 has been validated, which can be used immediately to investigate COVID-19 pathogenesis and test new therapies and vaccines. The study was supported by various grants from the National Institutes of Health and other organizations, and the data was generated using advanced technology purchased with funding from NIH.
Background:SARS-CoV-2, the virus responsible for COVID-19, causes widespread damage in the lungs in the setting of an overzealous immune response whose origin remains unclear.Methods:We present a scalable, propagable, personalized, cost-effective adult stem cell-derived human lung organoid model that is complete with both proximal and distal airway epithelia. Monolayers derived from adult lung organoids (ALOs), primary airway cells, or hiPSC-derived alveolar type II (AT2) pneumocytes were infected with SARS-CoV-2 to create in vitro lung models of COVID-19.Results:Infected ALO monolayers best recapitulated the transcriptomic signatures in diverse cohorts of COVID-19 patient-derived respiratory samples. The airway (proximal) cells were critical for sustained viral infection, whereas distal alveolar differentiation (AT2 -> AT1) was critical for mounting the overzealous host immune response in fatal disease; ALO monolayers with well-mixed proximodistal airway components recapitulated both.Conclusions:Findings validate a human lung model of COVID-19, which can be immediately utilized to investigate COVID-19 pathogenesis and vet new therapies and vaccines.Funding:This work was supported by the National Institutes for Health (NIH) grants 1R01DK107585-01A1, 3R01DK107585-05S1 (to SD); R01-AI141630, CA100768 and CA160911 (to PG) and R01-AI 155696 (to PG, DS and SD); R00-CA151673 and R01-GM138385 (to DS), R01- HL32225 (to PT), UCOP-R00RG2642 (to SD and PG), UCOP-R01RG3780 (to P.G. and D.S) and a pilot award from the Sanford Stem Cell Clinical Center at UC San Diego Health (P.G, S.D, D.S). GDK was supported through The American Association of Immunologists Intersect Fellowship Program for Computational Scientists and Immunologists. L.C.A's salary was supported in part by the VA San Diego Healthcare System. This manuscript includes data generated at the UC San Diego Institute of Genomic Medicine (IGC) using an Illumina NovaSeq 6000 that was purchased with funding from a National Institutes of Health SIG grant (#S10 OD026929).

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