Transcriptional landscape of TRPV1, TRPA1, TRPV4, and TRPM8 channels throughout human tissues

Life Sci. 2022 Nov 1:308:120977. doi: 10.1016/j.lfs.2022.120977. Epub 2022 Sep 17.

Abstract

Aims: This article aims to analyze the baseline distribution of TRPA1, TRPV1, TRPV4, and TRPM8 channels in human systems at the transcriptional level.

Main methods: Using the RNA-seq dataset from the National Center for Biotechnology Information (NCBI) gene database, we investigated and compared the transcriptional levels of TRPV1, TRPA1, TRPV4 and TRPM8 found in 95 human subjects representing 33 different tissues to determine the tissue specificity of all protein-coding genes.

Key finding: In this study, we observed higher transcriptional levels for TRPV1 (duodenum), TRPA1 (Urinary bladder), TRPV4 (Kidney) and TRPM8 (Prostate) compared to the other TRPs.

Significance: These channels are involved in developing inflammatory and painful pathologies and seem to participate in cancer development. This information on transcriptional levels of TRPV1, TRPA1, TRPV4 and TRPM8 in human systems may provide essential suggestions for further studies on these proteins.

Keywords: Bioinformatics; Biomarkers; Dorsal root ganglia; Drug development; RNA-sequencing; TRP channels.

MeSH terms

  • Humans
  • Male
  • Membrane Proteins / metabolism
  • TRPA1 Cation Channel / genetics
  • TRPM Cation Channels* / genetics
  • TRPM Cation Channels* / metabolism
  • TRPV Cation Channels / genetics
  • TRPV Cation Channels / metabolism
  • Transient Receptor Potential Channels* / genetics

Substances

  • Membrane Proteins
  • TRPA1 Cation Channel
  • TRPA1 protein, human
  • TRPM Cation Channels
  • TRPM8 channel-associated factor 1 protein, human
  • TRPM8 protein, human
  • TRPV Cation Channels
  • TRPV1 protein, human
  • TRPV4 protein, human
  • Transient Receptor Potential Channels