Expression profile of peripheral tissue antigen genes in medullary thymic epithelial cells (mTECs) is dependent on mRNA levels of autoimmune regulator (Aire)

Immunobiology. 2013 Jan;218(1):96-104. doi: 10.1016/j.imbio.2012.02.005. Epub 2012 Feb 14.

Abstract

In the thymus of non-obese diabetic (NOD) mice, the expression of the autoimmune regulator (Aire) gene varies with age, and its down-regulation in young mice precedes the later emergence of type 1 diabetes mellitus (T1D). In addition, the insulin (Ins2) peripheral tissue antigen (PTA) gene, which is Aire-dependent, is also deregulated in these mice. Based in these findings, we hypothesized that the imbalance in PTA gene expression in the thymus can be associated with slight variations in Aire transcript levels. To test this, we used siRNA to knockdown Aire by in vivo electro-transfection of the thymus of BALB/c mice. The efficiency of the electro-transfection was monitored by assessing the presence of irrelevant Cy3-labeled siRNA in the thymic stroma. Importantly, Aire-siRNA reached medullary thymic epithelial cells (mTECs) down-regulating Aire. As expected, the in vivo Aire knockdown was partial and transient; the maximum 59% inhibition occurred in 48 h. The Aire knockdown was sufficient to down-regulate PTA genes; however, surprisingly, several others, including Ins2, were up-regulated. The modulation of these genes after in vivo Aire knockdown was comparable to that observed in NOD mice before the emergence of T1D. The in vitro transfections of 3.10 mTEC cells with Aire siRNA resulted in samples featuring partial (69%) and complete (100%) Aire knockdown. In these Aire siRNA-transfected 3.10 mTECs, the expression of PTA genes, including Ins2, was down-regulated. This suggests that the expression profile of PTA genes in mTECs is affected by fine changes in the transcription level of Aire.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AIRE Protein
  • Animals
  • Cell Line
  • Collagen Type II / genetics
  • Collagen Type II / metabolism
  • Cytochrome P-450 CYP1A2 / genetics
  • Cytochrome P-450 CYP1A2 / metabolism
  • Diabetes Mellitus, Type 1 / genetics
  • Diabetes Mellitus, Type 1 / immunology*
  • Epithelial Cells / immunology*
  • Female
  • Gene Expression Regulation*
  • Humans
  • Insulin / genetics
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred NOD
  • RNA, Messenger / biosynthesis
  • RNA, Small Interfering / genetics
  • Thymus Gland / immunology
  • Thymus Gland / metabolism*
  • Transcription Factors / genetics*
  • Transcription, Genetic*
  • Transcriptome

Substances

  • Col2a1 protein, mouse
  • Collagen Type II
  • Ins2 protein, mouse
  • Insulin
  • RNA, Messenger
  • RNA, Small Interfering
  • Transcription Factors
  • Cytochrome P-450 CYP1A2