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Published on: April 21, 2015
IFN-gamma modulates CD1d surface expression on intestinal epithelia
S P Colgan1, V M Morales, J L Madara
1Department of Anesthesia, Brigham and Women's Hospital, Boston, Massachusetts 02215, USA.
Insights
Cytokines regulate CD1d expression on intestinal epithelial cells. Interferon-gamma (IFN-gamma) significantly increases CD1d mRNA and surface protein levels in these cells, impacting the intestinal immune microenvironment.
Area of Science:
- Immunology
- Gastroenterology
- Cell Biology
Background:
- Intestinal epithelial cells (IECs) interact closely with intestinal intraepithelial lymphocytes (iIELs).
- CD1d is a molecule on IECs potentially interacting with iIELs.
- Regulation of CD1d by cytokines in the intestinal environment is unknown.
Purpose of the Study:
- To investigate the impact of cytokines on CD1d expression in IECs.
- To determine if CD1d expression is regulated by cytokines at the mRNA and protein levels.
Main Methods:
- Utilized whole cell enzyme-linked immunosorbent assay (ELISA) to detect CD1d on intestinal epithelial cell lines (T84, Caco-2, HT-29).
- Exposed cell lines to human recombinant interferon-gamma (IFN-gamma).
- Analyzed CD1d mRNA levels using polymerase chain reaction (PCR) amplification of cDNA.
Main Results:
- CD1d was detected on the surface of T84 intestinal epithelial cells.
- IFN-gamma dose- and time-dependently increased CD1d surface expression and mRNA levels.
- This effect was specific to IFN-gamma and observed in multiple IEC lines (T84, Caco-2, HT-29).
- No significant surface expression of CD1a, CD1b, or CD1c was detected.
Conclusions:
- CD1d expression on IECs is regulated by cytokines, similar to major histocompatibility complex (MHC) molecules.
- IFN-gamma is a key regulator of CD1d expression in the intestinal epithelium.
- Findings provide insights into IEC-lymphocyte interactions within the intestinal microenvironment.
Abstract:
In vivo, epithelial cells that line the intestine are intimately associated with lymphocytes, termed intestinal intraepithelial lymphocytes (iIEL). A putative ligand for iIEL on intestinal epithelial cells is CD1d, and recent studies demonstrate a surface form of this molecule exists on intestinal epithelia. At present, it is not known whether CD1d expression is regulated by cytokines in the intestinal microenvironment. Thus we examined the impact of relevant cytokines on CD1d at the level of mRNA and cell surface expression. Using a sensitive whole cell enzyme-linked immunosorbent assay, we assessed the impact of relevant cytokines on CD1d expression on intestinal epithelial cell lines. We were readily able to detect CD1d on the surface of T84 cells, a cryptlike intestinal epithelial cell line. Epithelial cell exposure to human recombinant interferon-gamma (IFN-gamma) resulted in increased CD1d expression in a dose- and time-dependent manner. Polymerase chain reaction amplification of CD1d cDNA revealed a time-dependent induction after exposure to IFN-gamma. This IFN-gamma effect on CD1d expression was cytokine specific and was evident with epithelial cell lines other than T84, including Caco-2 and HT-29 cells. Finally, we were not able to detect significant surface expression of CD1a, CD1b, or CD1c on intestinal epithelial cell lines in the presence or absence of relevant cytokines. These results indicate that CD1d cell surface protein and cellular mRNA, like other major histocompatibility complex-related molecules, is cytokine regulated in intestinal epithelial cell lines.
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