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Updated: Aug 2, 2026

Isolation of Leukocytes from the Human Maternal-fetal Interface
Published on: May 21, 2015
Short-term cytolytic mediators' expression in decidual lymphocytes is enhanced by interleukin-15
Natasa Strbo1, Gordana Laskarin, Tatjana Bogovic Crncic
1Department of Physiology and Immunology, Medical Faculty, University of Rijeka, Rijeka, Croatia.
Insights
Interleukin-15 (IL-15) and decidual adherent cells (DAC) enhance the killing ability of first-trimester decidual lymphocytes (DL). IL-15, likely from DAC, boosts cytotoxic mediators and cell-killing potential, similar to IL-2.
Area of Science:
- Immunology
- Reproductive Biology
- Cell Biology
Background:
- Decidual lymphocytes (DL) play a crucial role in early pregnancy.
- The cytolytic potential of DL is critical for immune regulation during gestation.
- Decidual adherent cells (DAC) are a unique cell population in the decidua.
Purpose of the Study:
- To investigate the comparative effects of Interleukin-15 (IL-15) and Interleukin-2 (IL-2) on the cytolytic potential of first-trimester decidual lymphocytes (DL).
- To determine the role of decidual adherent cells (DAC) in modulating DL cytotoxicity.
- To explore the interplay between DAC, IL-15, and DL effector functions.
Main Methods:
- Decidual mononuclear cells were isolated and cultured with IL-15, IL-2, DAC, or anti-IL-15 antibody.
- Expression of cytotoxic mediators (perforin, FasL, granzyme B) was assessed at the mRNA level.
- Cytolytic activity of DL was measured using PKH-26 cytotoxicity assays against target cells (K-562, P815).
Main Results:
- IL-15 enhanced the transcription of perforin, FasL, and granzyme B in DL.
- DAC sustained perforin expression in DL, an effect abrogated by anti-IL-15 antibody.
- DAC significantly increased DL cytotoxicity against K-562 cells, mediated by IL-15.
Conclusions:
- IL-15, likely produced by DAC, upregulates cytotoxic mediators and enhances the perforin-mediated cytotoxicity of DL.
- The effect of IL-15 on DL cytotoxicity is comparable to that of high concentrations of IL-2.
- DAC play a significant role in regulating the immune function of decidual lymphocytes during early pregnancy.
Problem:
We investigated whether decidual adherent cells (DAC) and interleukin (IL)-15, in comparison to interleukin (IL)-2 affect cytolytic potential of first trimester decidual lymphocytes (DL).
Method Of Study:
Decidual mononuclear cells were obtained by enzymatic digestion and density gradient centrifugation. Non-adherent DL were collected after 2-hr adherence and cultured for 18 or 72 hr with: IL-15 (0.5-5 ng/mL), IL-2 (100-1000 U/mL) or both of these cytokines, DAC (ratio 3:1 and 1:1) or DAC and anti-IL-15 antibody. Perforin, Fas ligand (FasL) and granzyme B were detected at mRNA level in indicated culture conditions. Cytolytic activity of DL against K-562, P815 and P815-Fas was measured by 2-hr PKH-26 cytotoxicity assay. The dynamics of perforin protein and mRNA expression were measured in DL after a contact with K-562 targets.
Results:
Interleukin-15 enhanced perforin, FasL and granzyme B transcription after 18-hr culture and prevented perforin protein downregulation, observed after DL culture. IL-2 had similar effects. DAC sustained perforin expression in DL and anti-IL-15 monoclonal antibody abrogated this effect. DAC increased cytotoxicity of DL against K-562 which was mediated by IL-15.
Conclusion:
Interleukin-15, probably produced by DAC, upregulates cytolytic mediators' expression and perforin-mediated cytotoxicity of DL, with equal efficiency as high concentrations of IL-2.
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