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. 1986 Jul;58(3):379–387.

Functional characteristics of the veiled cells in afferent lymph from the rat intestine.

G Mayrhofer, P G Holt, J M Papadimitriou
PMCID: PMC1453468  PMID: 3525397

Abstract

Non-lymphoid veiled cells (VC) in the thoracic duct lymph from mesenteric lymphadenectomized rats have been studied by light microscopy, enzyme histochemistry and scanning electron microscopy. These cells arise in the afferent lymph from the intestine. They have been semi-purified and examined for expression of Ia antigens using an indirect immunoperoxidase technique and monoclonal antibodies. Accessory cell function necessary for mitogen-induced blastogenesis in the thoracic duct lymph from these animals has been correlated with the presence of VC by depletion and reconstitution experiments. Similar results were obtained with lymphocyte suspensions from other rat lymphoid organs and they are contrasted with those from studies on mouse lymphoid cells. Antigen presentation in a secondary in vitro lymphoproliferative assay was also depleted from immunized lymph node cells by removal of endogenous VC and can be reconstituted in a dose-dependent fashion with antigen-pulsed VC from afferent intestinal lymph. In contrast, reconstitution of both mitogen-induced blastogenesis and antigen-induced lymphoproliferation with peritoneal exudate cells was poor, while at high multiplicities of added macrophages, such cells were inhibitory. Afferent intestinal lymph VC were found to transport bacteria and bacterial antigen in rats infected with Salmonella typhimurium. The results are discussed in relation to the lineage of the VC in intestinal afferent lymph, their function as accessory cells and their possible physiological role in transporting antigens from the gut to its regional lymph nodes.

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Selected References

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  1. Allan W., Mayrhofer G. Origins of serum IgE and of the homocytotropic antibody-secreting cells in the thoracic duct lymph of rats infested with Nippostrongylus brasiliensis. Int Arch Allergy Appl Immunol. 1984;74(3):270–273. doi: 10.1159/000233556. [DOI] [PubMed] [Google Scholar]
  2. Barclay A. N. The localization of populations of lymphocytes defined by monoclonal antibodies in rat lymphoid tissues. Immunology. 1981 Apr;42(4):593–600. [PMC free article] [PubMed] [Google Scholar]
  3. Bell E. B. Antigen-laden cells in thoracic duct lymph. Implications for adoptive transfer experiments. Immunology. 1979 Dec;38(4):797–808. [PMC free article] [PubMed] [Google Scholar]
  4. Carter P. B., Collins F. M. The route of enteric infection in normal mice. J Exp Med. 1974 May 1;139(5):1189–1203. doi: 10.1084/jem.139.5.1189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Drexhage H. A., Mullink H., de Groot J., Clarke J., Balfour B. M. A study of cells present in peripheral lymph of pigs with special reference to a type of cell resembling the Langerhans cell. Cell Tissue Res. 1979 Nov;202(3):407–430. doi: 10.1007/BF00220434. [DOI] [PubMed] [Google Scholar]
  6. Hohmann A. W., Schmidt G., Rowley D. Intestinal colonization and virulence of Salmonella in mice. Infect Immun. 1978 Dec;22(3):763–770. doi: 10.1128/iai.22.3.763-770.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hohmann A., Schmidt G., Rowley D. Intestinal and serum antibody responses in mice after oral immunization with Salmonella, Escherichia coli, and Salmonella-Escherichia coli hybrid strains. Infect Immun. 1979 Jul;25(1):27–33. doi: 10.1128/iai.25.1.27-33.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Holt P. G. Alveolar macrophages. IV. Interspecies differences in activity in proliferating lymphocyte cultures. Cell Immunol. 1980 Mar 1;50(1):210–215. doi: 10.1016/0008-8749(80)90020-9. [DOI] [PubMed] [Google Scholar]
  9. Holt P. G., Warner L. A., Mayrhofer G. Macrophages as effectors of T suppression: T-lymphocyte-dependent macrophage-mediated suppression of mitogen-induced blastogenesis in the rat. Cell Immunol. 1981 Sep 1;63(1):57–70. doi: 10.1016/0008-8749(81)90028-9. [DOI] [PubMed] [Google Scholar]
  10. Hume D. A., Robinson A. P., MacPherson G. G., Gordon S. The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80. Relationship between macrophages, Langerhans cells, reticular cells, and dendritic cells in lymphoid and hematopoietic organs. J Exp Med. 1983 Nov 1;158(5):1522–1536. doi: 10.1084/jem.158.5.1522. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Husband A. J., Gowans J. L. The origin and antigen-dependent distribution of IgA-containing cells in the intestine. J Exp Med. 1978 Nov 1;148(5):1146–1160. doi: 10.1084/jem.148.5.1146. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Kaye P. M., Chain B. M., Feldmann M. Nonphagocytic dendritic cells are effective accessory cells for anti-mycobacterial responses in vitro. J Immunol. 1985 Mar;134(3):1930–1934. [PubMed] [Google Scholar]
  13. Klinkert W. E., LaBadie J. H., Bowers W. E. Accessory and stimulating properties of dendritic cells and macrophages isolated from various rat tissues. J Exp Med. 1982 Jul 1;156(1):1–19. doi: 10.1084/jem.156.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Langdon W. Y., Holt P. G., Shellam G. R. Antigen-pulsed macrophage monolayers as specific immunoabsorbents: selective absorption of murine T cells committed to soluble protein antigen. Immunology. 1981 Jul;43(3):555–562. [PMC free article] [PubMed] [Google Scholar]
  15. Lechler R. I., Batchelor J. R. Restoration of immunogenicity to passenger cell-depleted kidney allografts by the addition of donor strain dendritic cells. J Exp Med. 1982 Jan 1;155(1):31–41. doi: 10.1084/jem.155.1.31. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ly I. A., Mishell R. I. Separation of mouse spleen cells by passage through columns of sephadex G-10. J Immunol Methods. 1974 Aug;5(3):239–247. doi: 10.1016/0022-1759(74)90108-2. [DOI] [PubMed] [Google Scholar]
  17. MacDonald T. T., Carter P. B. Isolation and functional characteristics of adherent phagocytic cells from mouse Peyer's patches. Immunology. 1982 Apr;45(4):769–774. [PMC free article] [PubMed] [Google Scholar]
  18. Mayrhofer G., Fisher R. IgA-containing plasma cells in the lamina propria of the gut: failure of a thoracic duct fistula to deplete the numbers in rat small intestine. Eur J Immunol. 1979 Jan;9(1):85–91. doi: 10.1002/eji.1830090118. [DOI] [PubMed] [Google Scholar]
  19. Mayrhofer G., Pugh C. W., Barclay A. N. The distribution, ontogeny and origin in the rat of Ia-positive cells with dendritic morphology and of Ia antigen in epithelia, with special reference to the intestine. Eur J Immunol. 1983 Feb;13(2):112–122. doi: 10.1002/eji.1830130206. [DOI] [PubMed] [Google Scholar]
  20. Mayrhofer G., Schon-Hegrad M. A. Ia antigens in rat kidney, with special reference to their expression in tubular epithelium. J Exp Med. 1983 Jun 1;157(6):2097–2109. doi: 10.1084/jem.157.6.2097. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Perlmann H., Perlmann P., Pape G. R., Halldén G. Purification, fractionation and assay of antibody-dependent lymphocytic effector cells (K cells) in human blood. Scand J Immunol. 1976 Jun;Suppl 5:57–68. doi: 10.1111/j.1365-3083.1976.tb03856.x. [DOI] [PubMed] [Google Scholar]
  22. Pugh C. W., MacPherson G. G., Steer H. W. Characterization of nonlymphoid cells derived from rat peripheral lymph. J Exp Med. 1983 Jun 1;157(6):1758–1779. doi: 10.1084/jem.157.6.1758. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Richman L. K., Graeff A. S., Strober W. Antigen presentation by macrophage-enriched cells from the mouse Peyer's patch. Cell Immunol. 1981 Jul 15;62(1):110–118. doi: 10.1016/0008-8749(81)90304-x. [DOI] [PubMed] [Google Scholar]
  24. Schon-Hegrad M. A., Holt P. G. Improved method for the isolation of purified mouse peritoneal macrophages. J Immunol Methods. 1981;43(2):169–173. doi: 10.1016/0022-1759(81)90020-x. [DOI] [PubMed] [Google Scholar]
  25. Spalding D. M., Koopman W. J., Eldridge J. H., McGhee J. R., Steinman R. M. Accessory cells in murine Peyer's patch. I. Identification and enrichment of a functional dendritic cell. J Exp Med. 1983 May 1;157(5):1646–1659. doi: 10.1084/jem.157.5.1646. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Spalding D. M., Williamson S. I., Koopman W. J., McGhee J. R. Preferential induction of polyclonal IgA secretion by murine Peyer's patch dendritic cell-T cell mixtures. J Exp Med. 1984 Sep 1;160(3):941–946. doi: 10.1084/jem.160.3.941. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Spry C. J., Pflug A. J., Janossy G., Humphrey J. H. Large mononuclear (veiled) cells like 'Ia-like' membrane antigens in human afferent lympn. Clin Exp Immunol. 1980 Mar;39(3):750–755. [PMC free article] [PubMed] [Google Scholar]
  28. Steinman R. M., Cohn Z. A. Identification of a novel cell type in peripheral lymphoid organs of mice. I. Morphology, quantitation, tissue distribution. J Exp Med. 1973 May 1;137(5):1142–1162. doi: 10.1084/jem.137.5.1142. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Wilders M. M., Drexhage H. A., Weltevreden E. F., Mullink H., Duijvestijn A., Meuwissen S. G. Large mononuclear Ia-positive veiled cells in Peyer's patches. I. Isolation and characterization in rat, guinea-pig and pig. Immunology. 1983 Mar;48(3):453–460. [PMC free article] [PubMed] [Google Scholar]
  30. Wilders M. M., Sminia T., Plesch B. E., Drexhage H. A., Weltevreden E. F., Meuwissen S. G. Large mononuclear Ia-positive veiled cells in Peyer's patches. II. Localization in rat Peyer's patches. Immunology. 1983 Mar;48(3):461–467. [PMC free article] [PubMed] [Google Scholar]

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