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Single-cell transcriptomics of the mouse kidney reveals potential cellular targets of kidney disease
Author(s) -
Jihwan Park,
Rojesh Shrestha,
Chengxiang Qiu,
Ayano Kondo,
Shizheng Huang,
Max Werth,
Mingyao Li,
Jonathan Barasch,
Katalin Suszták
Publication year - 2018
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aar2131
Subject(s) - kidney , transcriptome , cell , disease , microbiology and biotechnology , biology , kidney disease , computational biology , medicine , pathology , genetics , gene , gene expression , endocrinology
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, Parket 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

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