Skip to main content
Log in

Carbon dioxide directly suppresses spontaneous migration, chemotaxis, and free radical production of human neutrophils

  • Published:
Surgical Endoscopy Aims and scope Submit manuscript

Abstract

Background

Carbon dioxide (CO2) insufflation during laparoscopy has been shown to dampen the systemic stress response to surgery. This is related to a suppression of peritoneal macrophage functions. In vivo data suggest that CO2 can also affect neutrophils (polymorphonuclear cells, PMNs), the most abundant cell type in the inflamed peritoneal cavity. Nonetheless, the direct effects of CO2 on PMNs have not yet been investigated.

Method

PMNs were isolated from peripheral blood of healthy volunteers and incubated with (1) CO2 (100% CO2, pH 6.2), (2) hypoxic control (95% helium/5% CO2, pH 7.4), and (3) control (95% air/5% CO2, pH 7.4). Spontaneous and IL-8-induced migrations (chemokinesis and chemotaxis) during 2 h of exposure to different gases were measured with a transwell chamber system. The release of reactive oxygen species (ROS, luminometry) was determined after 15-min and 2-h exposures. In other sets of experiments, PMNs were exposed for 2 h or 4 h and kept under normal conditions for 18 h with lipopolysaccharide (LPS) stimulation thereafter. Final viability and apoptosis were assessed with fluorometry.

Results

Exposure to 100% CO2 completely blocked spontaneous and IL-8 induced migration of PMNs (p < 0.001 vs. controls). Neutrophil migration was slightly diminished in the hypoxic control group. PMA-stimulated ROS production was reduced even after short exposure to 100% CO2 (p < 0.05). We observed a slight increase of caspase-3/7 activity after exposure to 100% CO2 and/or hypoxia; however, total viability was not affected.

Conclusions

CO2 incubation directly and temporarily suppresses the proinflammatory functions of PMNs; this is caused only partially by the concomitant hypoxia. This effect will contribute to the dampened inflammatory response to laparoscopic surgery. Further studies are needed to investigate whether the temporary suppression of neutrophil functions could affect the clearance of bacterial contaminations.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. Jesch NK, Kuebler JF, Nguyen H, Nave H, Bottlaender M, Teichmann B, Braun A, Vieten G, Ure BM (2006) Laparoscopy vs minilaparotomy and full laparotomy preserves circulatory but not peritoneal and pulmonary immune responses. J Pediatr Surg 41(6):1085–1092

    Article  PubMed  Google Scholar 

  2. Ure BM, Niewold TA, Bax NM, Ham M, van der Zee DC, Essen GJ (2002) Peritoneal, systemic, and distant organ inflammatory responses are reduced by a laparoscopic approach and carbon dioxide versus air. Surg Endosc 16(5):836–842

    Article  PubMed  CAS  Google Scholar 

  3. Rotstein OD (2001) Peritoneal host defenses: modulation by carbon dioxide insufflation. Surg Infect (Larchmt) 2(2):163–170

    Article  CAS  Google Scholar 

  4. Sylla P, Kirman I, Whelan RL (2005) Immunological advantages of advanced laparoscopy. Surg Clin North Am 85(1):1–18

    Article  PubMed  Google Scholar 

  5. Neuhaus SJ, Watson DI (2004) Pneumoperitoneum and peritoneal surface changes: a review. Surg Endosc 18(9):1316–1322

    Article  PubMed  CAS  Google Scholar 

  6. Sietses C, Wiezer MJ, Eijsbouts QA, van Leeuwen PA, Beelen RH, Meijer S, Cuesta MA (2000) The influence of laparoscopic surgery on postoperative polymorphonuclear leukocyte function. Surg Endosc 14(9):812–816

    Article  PubMed  CAS  Google Scholar 

  7. Neuhaus SJ, Gupta A, Watson DI (2001) Helium and other alternative insufflation gases for laparoscopy. Surg Endosc 15(6):553–560

    Article  PubMed  CAS  Google Scholar 

  8. Kopernik G, Avinoach E, Grossman Y, Levy R, Yulzari R, Rogachev B, Douvdevani A (1998) The effect of a high partial pressure of carbon dioxide environment on metabolism and immune functions of human peritoneal cells-relevance to carbon dioxide pneumoperitoneum. Am J Obstet Gynecol 179(6):1503–1510

    Article  PubMed  CAS  Google Scholar 

  9. Neuhaus SJ, Watson DI, Ellis T, Rofe AM, Mathew G, Jamieson GG (2000) Influence of gases on intraperitoneal immunity during laparoscopy in tumor-bearing rats. World J Surg 24(10):1227–1231

    Article  PubMed  CAS  Google Scholar 

  10. Kos M, Kuebler JF, Jesch NK, Vieten G, Bax NM, van der Zee DC, Busche R, Ure BM (2006) Carbon dioxide differentially affects the cytokine release of macrophage subpopulations exclusively via alteration of extracellular pH. Surg Endosc 20:570–576

    Article  PubMed  CAS  Google Scholar 

  11. Kuebler JF, Kos M, Jesch NK, Metzelder ML, van der Zee DC, Bax KM, Vieten G, Ure BM (2007) Carbon dioxide suppresses macrophage superoxide anion production independent of extracellular pH and mitochondrial activity. J Pediatr Surg 42:244–248

    Article  PubMed  Google Scholar 

  12. Menger MD, Vollmar B (2004) Surgical trauma: hyperinflammation versus immunosuppression? Langenbecks Arch Surg 389:475–484

    Article  PubMed  Google Scholar 

  13. Moehrlen U, Ziegler U, Boneberg E, Reichmann E, Gitzelmann CA, Meuli M, Hamacher J (2006) Impact of carbon dioxide versus air pneumoperitoneum on peritoneal cell migration and cell fate. Surg Endosc 20:1607–1613

    Article  PubMed  CAS  Google Scholar 

  14. Fukatsu K, Hiraide H (2003) [Role of polymorphonuclear neutrophils and macrophages in the prevention of postoperative infections] Nippon Geka Gakkai Zasshi 104:506–510 (in Japanese)

    PubMed  CAS  Google Scholar 

  15. Mercer-Jones MA, Shrotri MS, Heinzelmann M, Peyton JC, Cheadle WG (1999) Regulation of early peritoneal neutrophil migration by macrophage inflammatory protein-2 and mast cells in experimental peritonitis. J Leukoc Biol 65(2):249–255

    PubMed  CAS  Google Scholar 

  16. Knall C, Young S, Nick JA, Buhl AM, Worthen GS, Johnson GL (1996) Interleukin-8 regulation of the Ras/Raf/mitogen-activated protein kinase pathway in human neutrophils. J Biol Chem 271(5):2832–2838

    Article  PubMed  CAS  Google Scholar 

  17. Maianski NA, Maianski AN, Kuijpers TW, Roos D (2004) Apoptosis of neutrophils. Acta Haematol 111(1–2):56–66

    Article  PubMed  CAS  Google Scholar 

  18. Sawatzky DA, Willoughby DA, Colville-Nash PR, Rossi AG (2006) The involvement of the apoptosis-modulating proteins ERK 1/2, Bcl-xL and Bax in the resolution of acute inflammation in vivo. Am J Pathol 168(1):33–41

    Article  PubMed  CAS  Google Scholar 

  19. Rotstein OD, Fiegel VD, Simmons RL, Knighton DR (1988) The deleterious effect of reduced pH and hypoxia on neutrophil migration in vitro. J Surg Res 45(3):298–303

    Article  PubMed  CAS  Google Scholar 

  20. Cailhier JF, Partolina M, Vuthoori S, Wu S, Ko K, Watson S, Savill J, Hughes J, Lang RA (2005) Conditional macrophage ablation demonstrates that resident macrophages initiate acute peritoneal inflammation. J Immunol 174:2336–2342

    PubMed  CAS  Google Scholar 

  21. Ajuebor MN, Das AM, Virag L, Flower RJ, Szabo C, Perretti M (1999) Role of resident peritoneal macrophages and mast cells in chemokine production and neutrophil migration in acute inflammation: evidence for an inhibitory loop involving endogenous IL-10. J Immunol 162(3):1685–1691

    PubMed  CAS  Google Scholar 

  22. Colgan SP, Dzus AL, Parkos CA (1996) Epithelial exposure to hypoxia modulates neutrophil transepithelial migration. J Exp Med 184(3):1003–1015

    Article  PubMed  CAS  Google Scholar 

  23. Stein BN, Gamble JR, Pitson SM, Vadas MA, Khew-Goodall Y (2003) Activation of endothelial extracellular signal-regulated kinase is essential for neutrophil transmigration: potential involvement of a soluble neutrophil factor in endothelial activation. J Immunol 171(11):6097–6104

    PubMed  CAS  Google Scholar 

  24. Kuebler JF, Vieten G, Shimotakahara A, Metzelder ML, Jesch NK, Ure BM (2006) Acidification during carbon dioxide pneumoperitoneum is restricted to the gas-exposed peritoneal surface: effects of pressure, gas flow, and additional intraperitoneal fluids. J Laparoendosc Adv Surg Tech A 16(6):654–658

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

The authors thank Dr. Osamu Nagakawa, Department of Urology, Toyama University, Toyama, Japan, for his technical assistance. Akihiro Shimotakahara was supported by a grant from Deutsche Akademischer Austauschdienst and the Uehara Memorial Foundation.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Benno M. Ure.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Shimotakahara, A., Kuebler, J.F., Vieten, G. et al. Carbon dioxide directly suppresses spontaneous migration, chemotaxis, and free radical production of human neutrophils. Surg Endosc 22, 1813–1817 (2008). https://doi.org/10.1007/s00464-007-9703-0

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00464-007-9703-0

Keywords

Navigation