Transcriptional Activity of Genes Regulating T-Helper Differentiation in the Accidentally Exposed Population of the Southern Urals

Dokl Biochem Biophys. 2024 Dec;519(1):499-505. doi: 10.1134/S1607672924701114. Epub 2024 Sep 16.

Abstract

The objective of this work was to study the expression of the TBX21, RORC, GATA3, NFKB1, MAPK8, and STAT3 genes responsible for the regulation of the differentiation of various T-helper subpopulations in individuals chronically exposed to radiation. The object of the study was peripheral blood cells obtained from 120 persons chronically exposed to radiation in a wide range of doses on the Techa River. The mean cumulative absorbed dose to red bone marrow in the examined exposed individuals was 742.7 ± 78.6 mGy (dose range, 73.5-3516.1 mGy); in the comparison group, 17.4 ± 2.2 mGy (dose range, 0.0-55.5 mGy). The subpopulation composition of T-helpers (Th1, Th2, and Th17) was analyzed by flow cytofluorometry. The relative mRNA content of the TBX21, RORC, GATA3, NFKB1, MAPK8, and STAT3 genes was estimated by real-time PCR. The study made it possible to note a decrease in the relative number of T-helpers 2 in the populations of T-helpers of the central memory in the group of chronically exposed persons compared to the comparison group. In the population of T-helpers of the central memory, a statistically significant increase in the relative number of T-helpers 1 was shown, depending on the accumulated absorbed dose to red bone marrow. No changes in mRNA expression of the studied genes were observed. The analysis of the correlation between the expression of GATA3, MAPK8, STAT3, RORC, and TBX21 mRNA and the relative number of cells in subpopulations of T-helper types 1, 2, and 17 in the examined people did not reveal statistically significant patterns.

Keywords: T-helpers; Th1; Th17; Th2; chronic radiation exposure; gene expression; low and medium doses; the Techa River; transcriptional activity; transcriptional regulators of T-helper differentiation.

MeSH terms

  • Adult
  • Cell Differentiation*
  • Female
  • GATA3 Transcription Factor / genetics
  • GATA3 Transcription Factor / metabolism
  • Gene Expression Regulation / drug effects
  • Humans
  • Male
  • Middle Aged
  • NF-kappa B p50 Subunit* / genetics
  • NF-kappa B p50 Subunit* / metabolism
  • Nuclear Receptor Subfamily 1, Group F, Member 3* / genetics
  • Nuclear Receptor Subfamily 1, Group F, Member 3* / metabolism
  • Radiation Exposure / adverse effects
  • Russia
  • STAT3 Transcription Factor* / genetics
  • STAT3 Transcription Factor* / metabolism
  • T-Box Domain Proteins* / genetics
  • T-Box Domain Proteins* / metabolism
  • T-Lymphocytes, Helper-Inducer / drug effects
  • T-Lymphocytes, Helper-Inducer / metabolism
  • Transcription, Genetic / drug effects

Substances

  • Nuclear Receptor Subfamily 1, Group F, Member 3
  • T-Box Domain Proteins
  • STAT3 Transcription Factor
  • NF-kappa B p50 Subunit
  • GATA3 Transcription Factor
  • NFKB1 protein, human
  • RORC protein, human
  • GATA3 protein, human
  • STAT3 protein, human