Whole transcriptome profiling of taste bud cells

Sci Rep. 2017 Aug 8;7(1):7595. doi: 10.1038/s41598-017-07746-z.

Abstract

Analysis of single-cell RNA-Seq data can provide insights into the specific functions of individual cell types that compose complex tissues. Here, we examined gene expression in two distinct subpopulations of mouse taste cells: Tas1r3-expressing type II cells and physiologically identified type III cells. Our RNA-Seq libraries met high quality control standards and accurately captured differential expression of marker genes for type II (e.g. the Tas1r genes, Plcb2, Trpm5) and type III (e.g. Pkd2l1, Ncam, Snap25) taste cells. Bioinformatics analysis showed that genes regulating responses to stimuli were up-regulated in type II cells, while pathways related to neuronal function were up-regulated in type III cells. We also identified highly expressed genes and pathways associated with chemotaxis and axon guidance, providing new insights into the mechanisms underlying integration of new taste cells into the taste bud. We validated our results by immunohistochemically confirming expression of selected genes encoding synaptic (Cplx2 and Pclo) and semaphorin signalling pathway (Crmp2, PlexinB1, Fes and Sema4a) components. The approach described here could provide a comprehensive map of gene expression for all taste cell subpopulations and will be particularly relevant for cell types in taste buds and other tissues that can be identified only by physiological methods.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adaptor Proteins, Vesicular Transport / genetics
  • Adaptor Proteins, Vesicular Transport / metabolism
  • Animals
  • CD56 Antigen / genetics
  • CD56 Antigen / metabolism
  • Calcium Channels / genetics
  • Calcium Channels / metabolism
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism
  • Exome Sequencing
  • Gene Expression Profiling
  • Gene Expression Regulation*
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neuropeptides / genetics
  • Neuropeptides / metabolism
  • Phospholipase C beta / genetics
  • Phospholipase C beta / metabolism
  • Proto-Oncogene Proteins c-fes / genetics
  • Proto-Oncogene Proteins c-fes / metabolism
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Semaphorins / genetics
  • Semaphorins / metabolism
  • Signal Transduction
  • Single-Cell Analysis / methods
  • Synaptic Transmission / genetics
  • Synaptosomal-Associated Protein 25 / genetics
  • Synaptosomal-Associated Protein 25 / metabolism
  • TRPM Cation Channels / genetics
  • TRPM Cation Channels / metabolism
  • Taste / physiology*
  • Taste Buds / cytology
  • Taste Buds / metabolism*
  • Transcriptome*

Substances

  • Adaptor Proteins, Vesicular Transport
  • CD56 Antigen
  • Calcium Channels
  • Cytoskeletal Proteins
  • Intercellular Signaling Peptides and Proteins
  • Ncam1 protein, mouse
  • Nerve Tissue Proteins
  • Neuropeptides
  • Pclo protein, mouse
  • Pkd2l1 protein, mouse
  • Plxnb1 protein, mouse
  • Receptors, Cell Surface
  • Receptors, G-Protein-Coupled
  • Sema4A protein, mouse
  • Semaphorins
  • Snap25 protein, mouse
  • Synaptosomal-Associated Protein 25
  • TRPM Cation Channels
  • Trpm5 protein, mouse
  • collapsin response mediator protein-2
  • complexin II
  • taste receptors, type 1
  • Fes protein, mouse
  • Proto-Oncogene Proteins c-fes
  • Phospholipase C beta
  • Plcb2 protein, mouse