TY - JOUR
T1 - Spatially resolved transcriptomics and the kidney
T2 - many opportunities
AU - Dixon, Eryn E.
AU - Wu, Haojia
AU - Sulvarán-Guel, Elizabeth
AU - Guo, Juanru
AU - Humphreys, Benjamin D.
N1 - Funding Information:
BDH is a consultant for Janssen Research & Development, LLC, Pfizer, and Chinook Therapeutics, and holds equity in Chinook Therapeutics and grant funding from Chinook Therapeutics and Janssen Research & Development, LLC; none are related to the current work. All the other authors declared no competing interests.
Funding Information:
Funding in the Humphreys Lab is from the ReBuilding a Kidney Consortium grant UC2DK126024, DK103740-06, and the Chan Zuckerberg Initiative . EED is supported by F32DK130249.
Publisher Copyright:
© 2022 International Society of Nephrology
PY - 2022/9
Y1 - 2022/9
N2 - Defining changes in gene expression during health and disease is critical for the understanding of human physiology. In recent years, single-cell/nuclei RNA sequencing (sc/snRNAseq) has revolutionized the definition and discovery of cell types and states as well as the interpretation of organ- and cell-type–specific signaling pathways. However, these advances require tissue dissociation to the level of the single cell or single nuclei level. Spatially resolved transcriptomics (SrT) now provides a platform to overcome this barrier in understanding the physiological contexts of gene expression and cellular microenvironment changes in development and disease. Some of these transcriptomic tools allow for high-resolution mapping of hundreds of genes simultaneously in cellular and subcellular compartments. Other tools offer genome depth mapping but at lower resolution. We review advances in SrT, considerations for using SrT in your own research, and applications for kidney biology.
AB - Defining changes in gene expression during health and disease is critical for the understanding of human physiology. In recent years, single-cell/nuclei RNA sequencing (sc/snRNAseq) has revolutionized the definition and discovery of cell types and states as well as the interpretation of organ- and cell-type–specific signaling pathways. However, these advances require tissue dissociation to the level of the single cell or single nuclei level. Spatially resolved transcriptomics (SrT) now provides a platform to overcome this barrier in understanding the physiological contexts of gene expression and cellular microenvironment changes in development and disease. Some of these transcriptomic tools allow for high-resolution mapping of hundreds of genes simultaneously in cellular and subcellular compartments. Other tools offer genome depth mapping but at lower resolution. We review advances in SrT, considerations for using SrT in your own research, and applications for kidney biology.
KW - cell signaling
KW - histology
KW - transcription regulation
UR - http://www.scopus.com/inward/record.url?scp=85134760986&partnerID=8YFLogxK
U2 - 10.1016/j.kint.2022.06.011
DO - 10.1016/j.kint.2022.06.011
M3 - Short survey
C2 - 35788360
AN - SCOPUS:85134760986
SN - 0085-2538
VL - 102
SP - 482
EP - 491
JO - Kidney International
JF - Kidney International
IS - 3
ER -