Abstract
Previous studies demonstrated the presence of a small number of dendritic cells (DC), approximately 1%, in the peritoneal cavity of rats (1). Upon stimulation with either specific (e.g. Bacillus Calmette-Guérin, BCG) or non-specific stimuli (e.g. Thioglycollate Broth, TG) the number of DC had increased to 3% (2). Different studies demonstrated the superior capacity of peritoneal DC compared to peritoneal macrophages (MΦ) to present the antigen glutamine-tyrosine (GT) to GT-primed T cells in an in vitro assay (1,2,3), which is in agreement with other studies (4). Intraperitoneal stimulation with different stimuli had no effect on the antigen presenting capacity of DC, whereas that of the MΦ decreased, and especially after BCG M∅ had a suppressive effect on T cell proliferation. From these studies it was concluded that in the peritoneal cavity the DC was the major APC and although M∅ can act as APC, this function of M∅ strongly depends on the state of inflammation.
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Van Vugt, E., J.M.S. Arkema, M.A.M. Verdaasdonk, R.H.J. Beelen, and E.W.A.Kamperdijk.Morphological and functionalcharacteristics of rat steady state peritoneal dendritic cells. Immuno biol. 184; 14 (1991).
Van Vugt, E., M.A.M. Verdaasdonk, E.W.A. Kamperdijk, and R.H.J. Beelen. Antigenpresenting capacity of peritoneal macrophages and dendritic cells. Adv. Exp.Med. Biol. 329: 129 (1993).
Van Vugt, E., M.A.M. Verdaasdonk, R.H.J. Beelen, and E.W.A. Kamperdijk.Induction of an increased number ofdendritic cells in the peritoneal cavity of rats by intraperitonealadministration of Bacillus Calmette-Guerin. Immunobiol. 186: 230(1992).
Austyn, J.M.Lymphoid dendritic cells. Immunol. 62: 161 (1987).
Kampinga J.,F.G.M. Kroese, G.H. Pol, D. Opstelten, H.G. Seijen, J.H.A. Boot, B. Roser,P.Nieuwenhuis, and R. Aspinall. RT7-defined alloantigens in rats are part ofthe leucocyte common antigen family. Scand. J. Immunol. 31: 699 (1990).
Knight, SC.,J. Farrant, A. Bryant, A.J. Edwards, S. Burman, A. Lever,J. Clarke, and A.D.B.Webster. Non-adherent,low-density cells from human peripheral blood contain dendritic cells and monocytes,both with veiled morphology. Immunology 57: 595 (1986).
McMaster, W.R., and A.F. Williams. Identification of la glycoproteins in ratthymus and purification from rat spleen. Eur. J.Immunol. 9: 426 (1979).
Lawetzky, A., G. Tiefenthaler, R. Kubo and T. Hünig. Identification andcharacterization of rat T-cell subpopulations expressing T cell receptors α/ßand γ/ß. Eur.J.Immunol. 20: 343 (1990).
Cordell J.L., B. Faline, W.N. Erber, A.K. Ghosh, Z. Abdulaaiz, S. MacDonald,K.A.F. Pulford, H.Stein, and D.Y. Mason. Immunoenzymatic labeling of Monoclonalantibodies using immune complexes of alkaline phosphatase and monoclonalanti-alkaline phosphatase (APAAP Complexes). J. Histochem. and Cytochem.32:219(1984).
Kupiec-Weglinski, J.W., J.M. Austyn, and P.J. Morris. Migration patterns ofdendritic cells in the mouse. Traffic fromthe blood, and T cell-dependent and -independent entry to lymphoid tissues. J.Exp. Med.167: 632 (1988).
Inaba, K., J.P. Metlay, M.T. Crowley, and R.M. Steinman. Dendritic cells pulsedwith protein antigens in vitro can prime antigen-specific, MHC-restricted Tcells in situ. J.Exp.Med.172: 631 (1990).
Rosen H., and S. Gordon. Adoptive transfer of fluorescence-labeled cells showsthat resident peritoneal macrophages areable to migrate into specialized lymphoid organs and inflammatory sites inthe mouse. Eur. J. Immunol. 20: 1251 (1990).
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van Vugt, E., van Pelt, M., Beelen, R.H.J., Kamperdijk, E.W.A. (1995). Migration of Rat Dendritic Cells and Macrophages from the Peritoneal Cavity to the Parathymic Lymph Nodes. In: Banchereau, J., Schmitt, D. (eds) Dendritic Cells in Fundamental and Clinical Immunology. Advances in Experimental Medicine and Biology, vol 378. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-1971-3_36
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DOI: https://doi.org/10.1007/978-1-4615-1971-3_36
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