Skip to main content

Advertisement

Log in

Different inflammatory stimuli in the footpad of mice influence the kinetics of resident peritoneal cells

  • Original Research Paper
  • Published:
Inflammation Research Aims and scope Submit manuscript

Abstract

Objectives

Evidence from the literature that inflammation is a systemic biological phenomenon prompted us to investigate whether inoculation of different irritants to the footpad of mice might influence the kinetics of resident peritoneal cells.

Methods

Mice were inoculated in the footpad at different time intervals with Mycobacterium bovis bacillus Calmette-Guerin (BCG), Ehrlich ascitic tumor cells or lipopolysaccharide (LPS), and resident peritoneal cells were analyzed by flow cytometry.

Results

The results indicate that different stimuli induced different responses in resident peritoneal cells. FoxP3 positive regulatory T cells increased drastically in number after BCG inoculation. Conversely, tumor cell inoculation induced a decrease in FoxP3-positive T cells in the peritoneal cavity, although this effect was not statistically significant. Results also show that cells from the paw migrate to the popliteal lymph node and to the peritoneal cavity. Yet, there are cells in the peritoneal cavity that migrate to the popliteal lymph node.

Conclusion

These data show that cells from the peritoneal cavity are influenced by pathologies in remote regions of the animal. How this novel phenomenon influences overall immune responses, courses of infection and tumor growth are open to further investigation.

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
Fig. 5
Fig. 6
Fig. 7
Fig. 8

Similar content being viewed by others

References

  1. Lenzi HL, Oliveira DN, Borojevic R, Lenzi JA. Milky spots reaction to schistosomal mansoni infection. Mem Inst Oswaldo Cruz. 1992;87(Suppl 5):111–6.

    PubMed  Google Scholar 

  2. Lenzi HL, Oliveira DN, Pelajo-Machado M, Borojevic R, Lenzi JA. Coelom-associated lymphomyeloid tissue (milky spots): site of lymphoid and myelomonocytic cell generation. Braz J Med Biol Res. 1996;29:19–24.

    PubMed  CAS  Google Scholar 

  3. Panasco MS, Pelajo-Machado M, Lenzi HL. Omental and pleural milky spots: different reactivity patterns in mice infected with Schistosoma mansoni reveals coelomic compartmentalisation. Mem Inst Oswaldo Cruz. 2010;105:440–4.

    Article  PubMed  Google Scholar 

  4. Almeida SR, Aroeira LS, Frymuller E, Dias MA, Bogsan CS, Lopes JD, et al. Mouse B-1 cell-derived mononuclear phagocyte, a novel cellular component of acute non-specific inflammatory exudate. Int Immunol. 2001;13:1193–201.

    Article  PubMed  CAS  Google Scholar 

  5. Hayakawa K, Hardy RR, Parks DR, Herzenberg LA. The “Ly-1 B” cell subpopulation in normal immunodefective, and autoimmune mice. J Exp Med. 1983;157:202–18.

    Article  PubMed  CAS  Google Scholar 

  6. Staquicini FI, Tandle A, Libutti SK, Sun J, Zigler M, Bar-Eli M, et al. A subset of host B lymphocytes controls melanoma metastasis through a melanoma cell adhesion molecule/MUC18-dependent interaction: evidence from mice and humans. Cancer Res. 2008;68:8419–28.

    Article  PubMed  CAS  Google Scholar 

  7. Oliveira HC, Popi AF, Bachi AL, Nonogaki S, Lopes JD, Mariano M. B-1 cells modulate the kinetics of wound-healing process in mice. Immunobiology. 2010;215:215–22.

    Article  PubMed  CAS  Google Scholar 

  8. De Lorenzo BH, Brito RR, Godoy LC, Lopes JD, Mariano M. Tolerogenic property of B-1b cells in a model of allergic reaction. Immunol Lett. 2007;114:110–8.

    Article  PubMed  Google Scholar 

  9. Relvas WG, Izar MC, Segreto HR, Giordani AJ, Ihara SS, Mariano M, et al. Resident peritoneal inflammatory cells are pivotal in the development of experimental atherosclerosis. J Atheroscler Thromb. 2010;17:378–85.

    Article  PubMed  CAS  Google Scholar 

  10. Sinhorini IL, Merusse JL, Mariano M. Role of lymphatic drainage on the development of Calmette-Guerin bacillus-induced granulomas in the hamster. Int Arch Allergy Immunol. 1994;103:166–74.

    Article  PubMed  CAS  Google Scholar 

  11. Garcia-Leme J, Farsky SP. Hormonal control of inflammatory responses. Mediators Inflamm. 1993;2:181–98.

    Article  PubMed  CAS  Google Scholar 

  12. Hamamura L, Garcia Leme J. Neurogenic inflammation in the rat. Evidence for the release of a permeability factor from sensory nerves following electrical stimulation. Agents Actions. 1973;3:381–2.

    Article  PubMed  CAS  Google Scholar 

  13. Atkinson DC. A comparison of the systemic anti-inflammatory activity of three different irritants in the rat. Arch Int Pharmacodyn Ther. 1971;193:391–6.

    PubMed  CAS  Google Scholar 

  14. Atkinson DC, Hicks R. Relationship between the anti-inflammatory and irritant properties of inflammatory exudate. Br J Pharmacol. 1971;41:480–7.

    Article  PubMed  CAS  Google Scholar 

  15. Normann SJ, Schardt M, Sorkin E. Antileukocyte activity I. Systemic inhibition of cellular emigration following local inflammation. J Leukoc Biol. 1985;37:319–30.

    PubMed  CAS  Google Scholar 

Download references

Acknowledgments

We are indebted to Prof. Esper Kallás from the University of São Paulo for providing us with the use of the FlowJo program and the FACSCanto cytometer. We are also grateful for the skillful suggestions and comments of Mauro Nogueira Martins, Ronni Rômulo Novaes e Brito and Tatiana C. C. Oliveira. This work was supported by Fundação de Amparo à Pesquisa do Estado de São Paulo–FAPESP.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to M. Mariano.

Additional information

Responsible Editor: Michael Parnham.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Palos, M.C., Azevedo, M.C.A., Thies, F.G. et al. Different inflammatory stimuli in the footpad of mice influence the kinetics of resident peritoneal cells. Inflamm. Res. 61, 1187–1194 (2012). https://doi.org/10.1007/s00011-012-0514-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00011-012-0514-y

Keywords

Navigation