Spatially resolved transcriptomics and the kidney: many opportunities

Eryn E. Dixon, Haojia Wu, Elizabeth Sulvarán-Guel, Juanru Guo, Benjamin D. Humphreys

Research output: Contribution to journalShort surveypeer-review

2 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)482-491
Number of pages10
JournalKidney International
Volume102
Issue number3
DOIs
StatePublished - Sep 2022

Keywords

  • cell signaling
  • histology
  • transcription regulation

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