A reference tissue atlas for the human kidney
Author:
Hansen Jens, Sealfon Rachel, Menon Rajasree, Eadon Michael T., Lake Blue B., Steck Becky, Dobi Dejan, Parikh Samir, Sigdel Tara K., Zhang Guanshi, Velickovic Dusan, Barwinska Daria, Alexandrov TheodoreORCID, Rashmi Priyanka, Otto Edgar A., Rose Michael P., Anderton Christopher R., Shapiro John P., Pamreddy Annapurna, Winfree Seth, He YongqunORCID, de Boer Ian H., Hodgin Jeffrey B., Barisoni Laura, Naik Abhijit S., Sharma Kumar, Sarwal Minnie M., Zhang Kun, Himmelfarb Jonathan, Rovin Brad, El-Achkar Tarek M., Laszik Zoltan, He John Cijiang, Dagher Pierre C., Valerius M. Todd, Jain SanjayORCID, Satlin Lisa, Troyanskaya Olga G., Kretzler Matthias, Iyengar Ravi, Azeloglu Evren U.ORCID,
Abstract
AbstractKidney Precision Medicine Project (KPMP) is building a spatially-specified human tissue atlas at the single-cell resolution with molecular details of the kidney in health and disease. Here, we describe the construction of an integrated reference tissue map of cells, pathways and genes using unaffected regions of nephrectomy tissues and undiseased human biopsies from 55 subjects. We use single-cell and -nucleus transcriptomics, subsegmental laser microdissection bulk transcriptomics and proteomics, near-single-cell proteomics, 3-D nondestructive and CODEX imaging, and spatial metabolomics data to hierarchically identify genes, pathways and cells. Integrated data from these different technologies coherently describe cell types/subtypes within different nephron segments and interstitium. These spatial profiles identify cell-level functional organization of the kidney tissue as indicative of their physiological functions and map different cell subtypes to genes, proteins, metabolites and pathways. Comparison of transcellular sodium reabsorption along the nephron to levels of mRNAs encoding the different sodium transporter genes indicate that mRNA levels are largely congruent with physiological activity.This reference atlas provides an initial framework for molecular classification of kidney disease when multiple molecular mechanisms underlie convergent clinical phenotypes.
Publisher
Cold Spring Harbor Laboratory
Cited by
5 articles.
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