Title
A Single-Nucleus RNA-Sequencing Pipeline to Decipher the Molecular Anatomy and Pathophysiology of Human Kidneys.
Funding Source
National Institutes of Health
Grant Number
1 UG3 DK114933,U2CDK114886,DK085231
Department
Department of Physics and Computer Science - Dual Degree Engineering
Document Type
Article
Publication Date
6-27-2019
Abstract
Defining cellular and molecular identities within the kidney is necessary to understand its organization and function in health and disease. Here we demonstrate a reproducible method with minimal artifacts for single-nucleus Droplet-based RNA sequencing (snDrop-Seq) that we use to resolve thirty distinct cell populations in human adult kidney. We define molecular transition states along more than ten nephron segments spanning two major kidney regions. We further delineate cell type-specific expression of genes associated with chronic kidney disease, diabetes and hypertension, providing insight into possible targeted therapies. This includes expression of a hypertension-associated mechano-sensory ion channel in mesangial cells, and identification of proximal tubule cell populations defined by pathogenic expression signatures. Our fully optimized, quality-controlled transcriptomic profiling pipeline constitutes a tool for the generation of healthy and diseased molecular atlases applicable to clinical samples.
Recommended Citation
Lake, B. B.; Chen, S.; Hoshi, M.; Plongthongkum, N.; Salmon, D.; Knoten, A.; and Zhang, Kun, "A Single-Nucleus RNA-Sequencing Pipeline to Decipher the Molecular Anatomy and Pathophysiology of Human Kidneys." (2019). Faculty and Staff Publications. 81.
https://digitalcommons.xula.edu/fac_pub/81
Comments
DOI: 10.1038/s41467-019-10861-2
PubMed ID: 31249312