Expression profile and differential regulation of the Human I-mfa domain-Containing protein (HIC) gene in immune
Lili Gu1, Jonathan Dean, André L A Oliveira
1School of Medicine and Medical Science, Centre for Research in Infectious Diseases, University College Dublin, Belfield, Dublin 4, Ireland. lili.gu@ucd.ie
Insights
The Human I-mfa domain-Containing protein (HIC) is a transcriptional regulator highly expressed in immune cells. Interleukin-2 (IL-2) dynamically regulates HIC expression, suggesting a role in immune responses and potential tumor suppression.
Area of Science:
- Immunology
- Molecular Biology
- Cancer Research
Background:
- Human I-mfa domain-Containing protein (HIC) is a transcriptional regulator.
- HIC gene locus association with myeloid neoplasms and interactions with lymphotropic viruses suggest immune system involvement.
- HIC expression in immune tissues indicates a potential modulatory role in immune cells.
Purpose of the Study:
- To analyze HIC gene expression profile in immune cells.
- To determine if immunomodulatory cytokines, like interleukin-2 (IL-2), regulate HIC mRNA expression.
- To investigate the potential epigenetic control and tumor suppressor role of HIC.
Main Methods:
- Relative quantitative real-time RT-PCR to assess HIC mRNA expression.
- Treatment with IL-2 and cycloheximide to evaluate gene regulation.
- Use of DNA methyltransferase and histone-deacetylase inhibitors to study epigenetic control.
Main Results:
- HIC mRNA is highly expressed in peripheral blood mononuclear cells (PBMCs) and hematopoietic cell lines.
- IL-2 up-regulated HIC expression in most tested cells but reduced it in Raji cells, indicating cell-specific responses.
- IL-2's effect on HIC expression was independent of de novo protein synthesis, identifying HIC as a direct IL-2 target.
- Epigenetic inhibitors de-repressed HIC expression in cell lines with suppressed HIC, suggesting epigenetic regulation.
Conclusions:
- HIC immune expression is cell-specific and dynamic.
- HIC is an IL-2 responsive gene, highlighting its role in immune modulation.
- Epigenetic mechanisms likely control HIC expression.
- HIC may function as a tumor suppressor gene, relevant to hematological malignancies.
Abstract:
The Human I-mfa domain-Containing protein, HIC, is a 246 amino acid protein that functions as a transcriptional regulator. Although the precise function of HIC remains to be clarified, the association of the HIC gene locus with myeloid neoplasms, its interactions with lymphotropic viruses such as EBV, HIV-1 and HTLV-1 and its expression in immune tissues suggest that HIC might have a modulatory role in immune cells. To further characterise the HIC functional relationship with the immune system, we sought to analyse the HIC gene expression profile in immune cells and to determine if immunomodulatory cytokines, such as interleukin (IL)-2, could regulate the expression of HIC mRNA. Relative quantitative real-time RT-PCR revealed that HIC mRNA is highly expressed in PBMCs and in various hematopoietic cell lines. The immunomodulatory cytokine IL-2 up-regulated HIC gene expression in PBMCs, CEM, MT-2 and U937 but markedly reduced HIC gene expression in Raji. Addition of cycloheximide indicated that the IL-2 effects were independent of de novo protein synthesis and that the HIC gene is a direct target of IL-2. Two cell lines (Jurkat and BJAB) displayed a distinct loss in HIC gene expression. However, when these cell lines were subjected to a combination of DNA methyltransferase and histone-deacetylase inhibitors, (5-aza-2-deoxycytidine and trichostatin A, respectively), HIC expression was de-repressed, indicating possible epigenetic control of HIC expression. Overall, our study describes that the immune expression of HIC is cell-specific, dynamic, and identifies the HIC gene as an IL-2 responsive gene. Furthermore, our de-repression studies support the hypothesis that HIC might represent a candidate tumor suppressor gene. Overall, this report provides new insights for a putative role of HIC in the modulation of immune and inflammatory responses and/or hematological malignancies.
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