Expression of urokinase plasminogen activator receptor on monocytes and granulocytes is modulated by cardiac surgery
Jan Krejsek1, Martina Kolackova, Pavel Kunes
1Department of Clinical Immunology and Allergology, Charles University in Prague, School of Medicine and University Hospital in Hradec Kralove, Czech Republic. ukia@fnhk.cz
Insights
Cardiac surgery significantly alters urokinase plasminogen activator receptor (uPAR) expression on monocytes and granulocytes. This modulation occurs regardless of whether standard or mini-invasive cardiopulmonary bypass is used.
Area of Science:
- Cardiovascular Surgery
- Immunology
- Hematology
Background:
- Coronary artery bypass grafting (CABG) triggers the blood coagulation/fibrinolysis cascade, a key inflammatory response post-cardiac surgery.
- Understanding the role of urokinase plasminogen activator receptor (uPAR, CD87) in this process is crucial for managing post-surgical inflammation.
Purpose of the Study:
- To investigate the modulation of uPAR expression on monocytes and granulocytes in patients undergoing CABG.
- To compare uPAR expression changes between standard (
- on-pump
- ') and mini-invasive (
- mini on-pump
- ') cardiopulmonary bypass techniques.
Main Methods:
- Flow cytometry was used to measure uPAR expression (Median Fluorescence Intensity) on blood monocytes and granulocytes.
- uPAR expression levels were analyzed before, during, and after CABG surgery in both "on-pump" and "mini on-pump" patient groups.
Main Results:
- In "on-pump" patients, uPAR expression on granulocytes and monocytes significantly decreased post-surgery and during the first three days.
- In "mini on-pump" patients, uPAR expression on granulocytes and monocytes decreased significantly only after surgery.
- No significant differences in uPAR expression modulation were observed between "on-pump" and "mini on-pump" CABG procedures.
Conclusions:
- Cardiac surgery significantly modulates uPAR expression on both granulocytes and monocytes.
- The observed changes in uPAR expression suggest its involvement in the inflammatory response following CABG.
- The type of cardiopulmonary bypass (standard vs. mini-invasive) did not lead to significant differences in uPAR modulation.
Aims:
Coronary artery bypass grafting (CABG) is linked to the induction of the blood coagulation/fibrinolysis cascade, which is an integral component of inflammation induced by cardiac surgery. We followed the modulation of urokinase plasminogen activator receptor uPAR (CD87) separately for monocytes and granulocytes in blood of cardiac surgery patients.
Methods:
Expression of uPAR, analyzed as Median Fluorescence Intensity (MFI), on blood monocytes and granulocytes was determined by flow cytometry. Changes in uPAR expression in patients undergoing CABG using standard cardiopulmonary bypass ("on-pump") were compared to the changes in uPAR expression in patients undergoing CABG using mini-invasive cardiopulmonary bypass ("mini on-pump").
Results:
In "on-pump" patients, the median of uPAR expression on granulocytes before surgery was 18.1 (InterQuartile Range (IQR): 15.6-20.4). uPAR expression was significantly decreased after surgery (p<0.001), on the first postoperative day (p<0.001), and on the third postoperative day (p<0.05). In "mini on-pump" patients, the median of uPAR expression on granulocytes before surgery was 15.2 (IRQ: 13.8-19.4). The significantly decreased uPAR expression was found only at the end of surgery (p<0.05). The similar pattern of uPAR expression was also found for monocytes. The preoperative level in "on-pump" patients was 23.3 (IRQ: 18.9-30.2). There was significantly decreased uPAR expression at the end of surgery (p<0.01) and at the first postoperative day (p<0.05). In "mini on-pump" patients, the preoperative uPAR expression was 16.9 (IQR: 14.5-20.2). Expression of uPAR was significantly decreased only after surgery (p<0.05). When comparing "onpump" patients to "mini on-pump" patients, no significant differences in the expression of uPAR were found.
Conclusion:
uPAR expression on granulocytes and monocytes is significantly modulated by cardiac surgery.
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