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Article

Expression of CD11b (MAC-1) and CD162 (PSGL‑1) on monocytes is decreased under conditions of deep hypothermic circulatory arrest

  • Authors:
    • Stefanie Swoboda
    • Joachim Gruettner
    • Siegfried Lang
    • Hans-Peter Wendel
    • Martin E. Beyer
    • Eva Griesel
    • Hans-Martin Hoffmeister
    • Thomas Walter
  • View Affiliations / Copyright

    Affiliations: Pharmacy Department of the University Hospital of Heidelberg, Heidelberg, Germany, Emergency Department, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany, First Department of Medicine (Cardiology), University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany, Clinic for Thoracic, Cardiac and Vascular Surgery, University of Tuebingen, Tuebingen, Germany, Department of Internal Medicine II, Kirchheim Hospital, Kirchheim, Germany, Department of Internal Medicine II, Solingen Hospital, Solingen, Germany
  • Pages: 488-492
    |
    Published online on: May 28, 2014
       https://doi.org/10.3892/etm.2014.1737
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Abstract

Deep hypothermic circulatory arrest (DHCA) is a common technique used to protect vital organs during surgical interventions on the thoracic aorta or during surgery for complex congenital heart disease. Activated leukocytes are key mediators of inflammatory responses during ischemia. Intercellular crosstalk between leukocytes, platelets and endothelial cells is mediated by cell adhesion molecules. These molecules trigger complex cell-cell interaction mechanisms and initiate the release of proinflammatory molecules. One parameter that is known to have a significant impact on inflammatory cell activation and the production of proinflammatory markers is temperature. However, to the best of our knowledge, no data have yet been published on the effect of hypothermia on leukocyte surface markers during DHCA. Thus, the aim of the present study was to investigate the effect of hypothermia on the expression of cell adhesion molecules on monocytes under DHCA conditions in vitro. Blood samples collected from 11 healthy volunteers were incubated in a well-established model simulating circulatory arrest at 36˚C and 18˚C for 30 min. The expression of cluster of differentiation (CD) molecule 11B (CD11b), CD54 and CD162 on monocytes was measured as the mean fluorescence intensity (MFI) using flow cytometry. The expression level of CD11b on monocytes was significantly decreased following the incubation of the blood samples at 18˚C compared with the level in blood samples incubated at 36˚C (P<0.001). After 30 min of blood stasis in the circulatory arrest model, the expression level of CD162 on monocytes was significantly lower in the blood samples incubated at 18˚C than in those incubated at 36˚C (P<0.001). No association was identified between temperature and the surface expression of CD54 on monocytes following 30 min of stasis. These findings demonstrate that deep hypothermia decreases the expression of CD11b and CD162 on monocytes in an experimental setup simulating the conditions of DHCA. This may be the result of the inhibition of leukocyte‑endothelial and leukocyte-platelet interactions, which may be a beneficial aspect of deep hypothermia that affects the inflammatory response and tissue damage during DHCA.
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Copy and paste a formatted citation
Spandidos Publications style
Swoboda S, Gruettner J, Lang S, Wendel H, Beyer ME, Griesel E, Hoffmeister H and Walter T: Expression of CD11b (MAC-1) and CD162 (PSGL‑1) on monocytes is decreased under conditions of deep hypothermic circulatory arrest. Exp Ther Med 8: 488-492, 2014.
APA
Swoboda, S., Gruettner, J., Lang, S., Wendel, H., Beyer, M.E., Griesel, E. ... Walter, T. (2014). Expression of CD11b (MAC-1) and CD162 (PSGL‑1) on monocytes is decreased under conditions of deep hypothermic circulatory arrest. Experimental and Therapeutic Medicine, 8, 488-492. https://doi.org/10.3892/etm.2014.1737
MLA
Swoboda, S., Gruettner, J., Lang, S., Wendel, H., Beyer, M. E., Griesel, E., Hoffmeister, H., Walter, T."Expression of CD11b (MAC-1) and CD162 (PSGL‑1) on monocytes is decreased under conditions of deep hypothermic circulatory arrest". Experimental and Therapeutic Medicine 8.2 (2014): 488-492.
Chicago
Swoboda, S., Gruettner, J., Lang, S., Wendel, H., Beyer, M. E., Griesel, E., Hoffmeister, H., Walter, T."Expression of CD11b (MAC-1) and CD162 (PSGL‑1) on monocytes is decreased under conditions of deep hypothermic circulatory arrest". Experimental and Therapeutic Medicine 8, no. 2 (2014): 488-492. https://doi.org/10.3892/etm.2014.1737
Copy and paste a formatted citation
x
Spandidos Publications style
Swoboda S, Gruettner J, Lang S, Wendel H, Beyer ME, Griesel E, Hoffmeister H and Walter T: Expression of CD11b (MAC-1) and CD162 (PSGL‑1) on monocytes is decreased under conditions of deep hypothermic circulatory arrest. Exp Ther Med 8: 488-492, 2014.
APA
Swoboda, S., Gruettner, J., Lang, S., Wendel, H., Beyer, M.E., Griesel, E. ... Walter, T. (2014). Expression of CD11b (MAC-1) and CD162 (PSGL‑1) on monocytes is decreased under conditions of deep hypothermic circulatory arrest. Experimental and Therapeutic Medicine, 8, 488-492. https://doi.org/10.3892/etm.2014.1737
MLA
Swoboda, S., Gruettner, J., Lang, S., Wendel, H., Beyer, M. E., Griesel, E., Hoffmeister, H., Walter, T."Expression of CD11b (MAC-1) and CD162 (PSGL‑1) on monocytes is decreased under conditions of deep hypothermic circulatory arrest". Experimental and Therapeutic Medicine 8.2 (2014): 488-492.
Chicago
Swoboda, S., Gruettner, J., Lang, S., Wendel, H., Beyer, M. E., Griesel, E., Hoffmeister, H., Walter, T."Expression of CD11b (MAC-1) and CD162 (PSGL‑1) on monocytes is decreased under conditions of deep hypothermic circulatory arrest". Experimental and Therapeutic Medicine 8, no. 2 (2014): 488-492. https://doi.org/10.3892/etm.2014.1737
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