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Single-cell RNA sequencing reveals the mesangial identity and species diversity of glomerular cell transcriptomes

Author

Listed:
  • Bing He

    (Karolinska Institute/AstraZeneca Integrated Cardio Metabolic Center (ICMC))

  • Ping Chen

    (Karolinska Institute/AstraZeneca Integrated Cardio Metabolic Center (ICMC))

  • Sonia Zambrano

    (Karolinska Institute/AstraZeneca Integrated Cardio Metabolic Center (ICMC)
    Karolinska University Hospital Huddinge)

  • Dina Dabaghie

    (Karolinska Institute/AstraZeneca Integrated Cardio Metabolic Center (ICMC)
    Karolinska University Hospital Huddinge)

  • Yizhou Hu

    (Division of Neuroscience, Department of Medical Biochemistry and Biophysics (MBB), Karolinska Institute)

  • Katja Möller-Hackbarth

    (Karolinska Institute/AstraZeneca Integrated Cardio Metabolic Center (ICMC))

  • David Unnersjö-Jess

    (University of Cologne
    University of Cologne)

  • Gül Gizem Korkut

    (Karolinska Institute/AstraZeneca Integrated Cardio Metabolic Center (ICMC))

  • Emmanuelle Charrin

    (Karolinska Institute/AstraZeneca Integrated Cardio Metabolic Center (ICMC)
    Karolinska University Hospital Huddinge)

  • Marie Jeansson

    (Karolinska Institute/AstraZeneca Integrated Cardio Metabolic Center (ICMC))

  • Maria Bintanel-Morcillo

    (Karolinska Institute/AstraZeneca Integrated Cardio Metabolic Center (ICMC)
    Karolinska University Hospital Huddinge)

  • Anna Witasp

    (Division of Renal Medicine, Department of Clinical Sciences, Intervention and Technology, Karolinska Institute)

  • Lars Wennberg

    (Division of Transplantation, Department of Clinical Sciences, Intervention and Technology, Karolinska Institute)

  • Annika Wernerson

    (Division of Renal Medicine, Department of Clinical Sciences, Intervention and Technology, Karolinska Institute)

  • Bernhard Schermer

    (University of Cologne
    University of Cologne)

  • Thomas Benzing

    (University of Cologne
    University of Cologne)

  • Patrik Ernfors

    (Division of Neuroscience, Department of Medical Biochemistry and Biophysics (MBB), Karolinska Institute)

  • Christer Betsholtz

    (Karolinska Institute/AstraZeneca Integrated Cardio Metabolic Center (ICMC)
    Uppsala University)

  • Mark Lal

    (Bioscience, Cardiovascular, Renal and Metabolism, R&D Biopharmaceuticals)

  • Rickard Sandberg

    (Department of Cell and Molecular Biology, Karolinska Institute)

  • Jaakko Patrakka

    (Karolinska Institute/AstraZeneca Integrated Cardio Metabolic Center (ICMC)
    Karolinska University Hospital Huddinge)

Abstract

Molecular characterization of the individual cell types in human kidney as well as model organisms are critical in defining organ function and understanding translational aspects of biomedical research. Previous studies have uncovered gene expression profiles of several kidney glomerular cell types, however, important cells, including mesangial (MCs) and glomerular parietal epithelial cells (PECs), are missing or incompletely described, and a systematic comparison between mouse and human kidney is lacking. To this end, we use Smart-seq2 to profile 4332 individual glomerulus-associated cells isolated from human living donor renal biopsies and mouse kidney. The analysis reveals genetic programs for all four glomerular cell types (podocytes, glomerular endothelial cells, MCs and PECs) as well as rare glomerulus-associated macula densa cells. Importantly, we detect heterogeneity in glomerulus-associated Pdgfrb-expressing cells, including bona fide intraglomerular MCs with the functionally active phagocytic molecular machinery, as well as a unique mural cell type located in the central stalk region of the glomerulus tuft. Furthermore, we observe remarkable species differences in the individual gene expression profiles of defined glomerular cell types that highlight translational challenges in the field and provide a guide to design translational studies.

Suggested Citation

  • Bing He & Ping Chen & Sonia Zambrano & Dina Dabaghie & Yizhou Hu & Katja Möller-Hackbarth & David Unnersjö-Jess & Gül Gizem Korkut & Emmanuelle Charrin & Marie Jeansson & Maria Bintanel-Morcillo & Ann, 2021. "Single-cell RNA sequencing reveals the mesangial identity and species diversity of glomerular cell transcriptomes," Nature Communications, Nature, vol. 12(1), pages 1-19, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-22331-9
    DOI: 10.1038/s41467-021-22331-9
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    Cited by:

    1. Wiebke Sachs & Lukas Blume & Desiree Loreth & Lisa Schebsdat & Favian Hatje & Sybille Koehler & Uta Wedekind & Marlies Sachs & Stephanie Zieliniski & Johannes Brand & Christian Conze & Bogdan I. Flore, 2024. "The proteasome modulates endocytosis specifically in glomerular cells to promote kidney filtration," Nature Communications, Nature, vol. 15(1), pages 1-21, December.
    2. Ziye Xu & Tianyu Zhang & Hongyu Chen & Yuyi Zhu & Yuexiao Lv & Shunji Zhang & Jiaye Chen & Haide Chen & Lili Yang & Weiqin Jiang & Shengyu Ni & Fangru Lu & Zhaolun Wang & Hao Yang & Ling Dong & Feng C, 2023. "High-throughput single nucleus total RNA sequencing of formalin-fixed paraffin-embedded tissues by snRandom-seq," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    3. Taryn D. Treger & John E. G. Lawrence & Nathaniel D. Anderson & Tim H. H. Coorens & Aleksandra Letunovska & Emilie Abby & Henry Lee-Six & Thomas R. W. Oliver & Reem Al-Saadi & Kjell Tullus & Guillaume, 2023. "Targetable NOTCH1 rearrangements in reninoma," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
    4. Urban Lendahl & Lars Muhl & Christer Betsholtz, 2022. "Identification, discrimination and heterogeneity of fibroblasts," Nature Communications, Nature, vol. 13(1), pages 1-14, December.

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