Cell profiling of mouse acute kidney injury reveals conserved cellular responses to injury

  • Yuhei Kirita
    Division of Nephrology, Department of Medicine, Washington University in Saint Louis School of Medicine, St. Louis, MO 63110;
  • Haojia Wu
    Division of Nephrology, Department of Medicine, Washington University in Saint Louis School of Medicine, St. Louis, MO 63110;
  • Kohei Uchimura
    Division of Nephrology, Department of Medicine, Washington University in Saint Louis School of Medicine, St. Louis, MO 63110;
  • Parker C. Wilson
    Division of Anatomic and Molecular Pathology, Department of Pathology and Immunology, Washington University in Saint Louis School of Medicine, St. Louis, MO 63110;
  • Benjamin D. Humphreys
    Division of Nephrology, Department of Medicine, Washington University in Saint Louis School of Medicine, St. Louis, MO 63110;

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<jats:title>Significance</jats:title> <jats:p>Single nucleus RNA sequencing revealed gene expression changes during repair after acute kidney injury. We describe a small population of proximal tubule cells that fail to repair (FR-PTCs). Since this subpopulation expresses abundant proinflammatory and profibrotic genes, it may represent a new therapeutic target to improve repair and reduce fibrosis after AKI.</jats:p>

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