Single-cell transcriptomics of the mouse kidney reveals potential cellular targets of kidney disease

Author:

Park Jihwan1ORCID,Shrestha Rojesh1ORCID,Qiu Chengxiang1ORCID,Kondo Ayano1ORCID,Huang Shizheng1ORCID,Werth Max2ORCID,Li Mingyao3,Barasch Jonathan2ORCID,Suszták Katalin1ORCID

Affiliation:

1. Renal Electrolyte and Hypertension Division, Department of Medicine and Genetics, University of Pennsylvania, Philadelphia, PA 19104, USA.

2. Renal Division, Department of Medicine, Columbia University, New York, NY 10032, USA.

3. Department of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA 19104, USA.

Abstract

Touring the kidney, cell by cell Our kidneys play a critical role in keeping us healthy, a fact of which we are reminded several times each day. This organ's cellular complexity has hindered progress in understanding the mechanisms underlying chronic kidney disease, which affects 10% of the world's population. Using single-cell transcriptional profiling, Park et al. produced a comprehensive cell atlas of the healthy mouse kidney (see the Perspective by Humphreys). An unexpected cell type in the collecting duct appears to be a transitional state between two known cell types. The transition from one cell type to the other is regulated by the Notch signaling pathway and is associated with metabolic acidosis. The authors also find that genetically distinct kidney diseases with common clinical features share common cellular origins. Science , this issue p. 758 ; see also p. 709

Funder

National Institutes of Health

American Diabetes Association

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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