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Single-cell transcriptomics reveals common epithelial response patterns in human acute kidney injury.
Hinze, Christian; Kocks, Christine; Leiz, Janna; Karaiskos, Nikos; Boltengagen, Anastasiya; Cao, Shuang; Skopnik, Christopher Mark; Klocke, Jan; Hardenberg, Jan-Hendrik; Stockmann, Helena; Gotthardt, Inka; Obermayer, Benedikt; Haghverdi, Laleh; Wyler, Emanuel; Landthaler, Markus; Bachmann, Sebastian; Hocke, Andreas C; Corman, Victor; Busch, Jonas; Schneider, Wolfgang; Himmerkus, Nina; Bleich, Markus; Eckardt, Kai-Uwe; Enghard, Philipp; Rajewsky, Nikolaus; Schmidt-Ott, Kai M.
Afiliação
  • Hinze C; Department of Nephrology and Hypertension, Hannover Medical School, Hannover, Germany.
  • Kocks C; Department of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Berlin, Germany.
  • Leiz J; Max Delbrueck Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
  • Karaiskos N; Berlin Institute for Medical Systems Biology, Max Delbrueck Center in the Helmholtz Association, Berlin, Germany.
  • Boltengagen A; Department of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Berlin, Germany.
  • Cao S; Max Delbrueck Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
  • Skopnik CM; Berlin Institute for Medical Systems Biology, Max Delbrueck Center in the Helmholtz Association, Berlin, Germany.
  • Klocke J; Berlin Institute for Medical Systems Biology, Max Delbrueck Center in the Helmholtz Association, Berlin, Germany.
  • Hardenberg JH; Department of Nephrology and Hypertension, Hannover Medical School, Hannover, Germany.
  • Stockmann H; Department of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Berlin, Germany.
  • Gotthardt I; Max Delbrueck Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
  • Obermayer B; Department of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Berlin, Germany.
  • Haghverdi L; Deutsches Rheumaforschungszentrum, an Institute of the Leibniz Foundation, Berlin, Germany.
  • Wyler E; Department of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Berlin, Germany.
  • Landthaler M; Deutsches Rheumaforschungszentrum, an Institute of the Leibniz Foundation, Berlin, Germany.
  • Bachmann S; Berlin Institute of Health, Berlin, Germany.
  • Hocke AC; Department of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Berlin, Germany.
  • Corman V; Department of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Berlin, Germany.
  • Busch J; Department of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Berlin, Germany.
  • Schneider W; Core Unit Bioinformatics, BIH/Charité/MDC, Berlin, Germany.
  • Himmerkus N; Berlin Institute for Medical Systems Biology, Max Delbrueck Center in the Helmholtz Association, Berlin, Germany.
  • Bleich M; Berlin Institute for Medical Systems Biology, Max Delbrueck Center in the Helmholtz Association, Berlin, Germany.
  • Eckardt KU; Berlin Institute for Medical Systems Biology, Max Delbrueck Center in the Helmholtz Association, Berlin, Germany.
  • Enghard P; Institute for Functional Anatomy, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Berlin, Germany.
  • Rajewsky N; Berlin Institute of Health, Berlin, Germany.
  • Schmidt-Ott KM; Department of Infectious Diseases and Respiratory Medicine, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Berlin, Germany.
Genome Med ; 14(1): 103, 2022 09 09.
Article em En | MEDLINE | ID: mdl-36085050
BACKGROUND: Acute kidney injury (AKI) occurs frequently in critically ill patients and is associated with adverse outcomes. Cellular mechanisms underlying AKI and kidney cell responses to injury remain incompletely understood. METHODS: We performed single-nuclei transcriptomics, bulk transcriptomics, molecular imaging studies, and conventional histology on kidney tissues from 8 individuals with severe AKI (stage 2 or 3 according to Kidney Disease: Improving Global Outcomes (KDIGO) criteria). Specimens were obtained within 1-2 h after individuals had succumbed to critical illness associated with respiratory infections, with 4 of 8 individuals diagnosed with COVID-19. Control kidney tissues were obtained post-mortem or after nephrectomy from individuals without AKI. RESULTS: High-depth single cell-resolved gene expression data of human kidneys affected by AKI revealed enrichment of novel injury-associated cell states within the major cell types of the tubular epithelium, in particular in proximal tubules, thick ascending limbs, and distal convoluted tubules. Four distinct, hierarchically interconnected injured cell states were distinguishable and characterized by transcriptome patterns associated with oxidative stress, hypoxia, interferon response, and epithelial-to-mesenchymal transition, respectively. Transcriptome differences between individuals with AKI were driven primarily by the cell type-specific abundance of these four injury subtypes rather than by private molecular responses. AKI-associated changes in gene expression between individuals with and without COVID-19 were similar. CONCLUSIONS: The study provides an extensive resource of the cell type-specific transcriptomic responses associated with critical illness-associated AKI in humans, highlighting recurrent disease-associated signatures and inter-individual heterogeneity. Personalized molecular disease assessment in human AKI may foster the development of tailored therapies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Injúria Renal Aguda / COVID-19 Limite: Humans Idioma: En Revista: Genome Med Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Injúria Renal Aguda / COVID-19 Limite: Humans Idioma: En Revista: Genome Med Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha