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Updated: May 28, 2026

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Published on: August 17, 2022
Granulysin Expression in Lymphocytes that Populate the Peripheral Blood and the Myocardium after an Acute Coronary
V Persic1, A Ruzic1, B Miletic1
1Division of Cardiology, Hospital for Medical Rehabilitation of the Hearth and Lung Diseases and Rheumatism "Thalassotherapija" Opatija, Opatija, CroatiaDepartment of Medical Rehabilitation, Medical Faculty, University of Rijeka, Rijeka, CroatiaDepartment of Pathology, Medical Faculty, University of Rijeka, Rijeka, CroatiaDivision of Cardiology Clinical Hospital Center Rijeka, Rijeka, CroatiaDepartment of Internal Medicine, Medical Faculty, University of Rijeka, Rijeka, CroatiaDepartment of Physiology and Immunology, Medical Faculty, University of Rijeka, Rijeka, Croatia.
Insights
Granulysin (GNLY) expressing lymphocytes increase after myocardial infarction (MI), contributing to cardiac cell apoptosis and aiding leukocyte resolution. Their levels normalize by day 28 post-MI.
Area of Science:
- Immunology
- Cardiology
- Cell Biology
Background:
- Non-ST-segment elevation myocardial infarction (NSTEMI) involves complex immune responses.
- Granulysin (GNLY) is a cytotoxic protein implicated in immune cell function.
Purpose of the Study:
- To analyze granulysin (GNLY)-mediated cytotoxicity in peripheral blood of NSTEMI patients.
- To investigate the role of GNLY(+) lymphocytes in myocardial infarction (MI) pathogenesis and resolution.
Main Methods:
- Flow cytometry was used to quantify GNLY(+) lymphocytes in NSTEMI patients and healthy controls.
- Immunohistology examined GNLY(+) cell infiltration in myocardial tissue.
- In vitro assays assessed the cytotoxic effects of GNLY and perforin.
Main Results:
- GNLY(+) lymphocytes significantly increased in NSTEMI patients by day 7 post-MI.
- These cells infiltrated infarct zones and were associated with cardiomyocyte apoptosis.
- GNLY contributed to target cell apoptosis, with varying dependence on perforin over time.
Conclusions:
- GNLY(+) lymphocytes play a role in myocardial cell apoptosis and accelerate leukocyte infiltration resolution post-NSTEMI.
- Interleukin-15 may attract GNLY(+) lymphocytes to infarct areas.
- Understanding GNLY's role offers insights into NSTEMI immune dynamics.
Abstract:
We aimed to analyse granulysin (GNLY)-mediated cytotoxicity in the peripheral blood of patients with non-ST-segment elevation myocardial infarction (NSTEMI) treated with anti-ischaemic drug therapy. Thirty-nine NSTEMI patients with a median age of 70 years and 28 age-matched healthy subjects were enrolled in this study. On day 7 after MI, the number of GNLY(+) lymphocytes in the peripheral blood increased approximately six-fold of that in the healthy subjects, measured by flow cytometry. On day 14, the number of GNLY(+) cells significantly decreased in T, NKT, and both CD56(+dim) and CD56(+bright) NK subsets. GNLY(+) CD3(+) and GNLY(+) CD56(+) cells infiltrated central zone of myocardial infarction (MI). In persons who died in the first week after MI, GNLY(+) cells were found within accumulation of apoptotic leucocytes and reached the apoptotic cardiomyocytes in border MI zones probably due to the influence of interleukin-15 in peri-necrotic cardiomyocytes, as it is was shown by immunohistology. By day 28, the percentage of GNLY(+) lymphocytes in peripheral blood returned to the levels similar to that of the healthy subjects. Anti-GNLY mAb decreased apoptosis of K562 targets using peripheral blood NK cells from days 7 and 28 after MI, while in assays using cells from days 1 and 21, both anti-GNLY and anti-perforin mAbs were required to significantly decrease apoptosis. Using NK cells from day 14, K562 apoptosis was nearly absent. In conclusion, it seems that GNLY(+) lymphocytes, probably attracted by IL-15, not only participate partially in myocardial cell apoptosis, but also hasten resolution of cardiac leucocyte infiltration in patients with NSTEMI.
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