Virchows Archiv B

, 35:63 | Cite as

Morphological changes in paracortical high endothelial venules to single and repeated application of oxazolone to mouse skin

  • Andreas O. Myking
Article

Summary

Morphological changes in paracortical high endothelial venules (HEV) have been studied after single and repeated applications of oxazolone to mouse skin. The primary response was characterized by a rapid and marked vascular dilatation, by marked increase in the cross sectional area of the vessel wall and in the size of the individual endothelial cells, as well as increased accumulation of lymphocytes in HEV walls. These changes regressed (in the more long lasting response). The transitory structural alterations may be related to increase of blood flow, increased flow of cells from the thymus to the stimulated lymph nodes as well as increased transport capacity of endothelial cells based on augmentation of their surface area. These features are closely related to other cellular events such as a prominent blastoid reaction in the paracortex as well as an associated cellular depletion of the thymus.

Key words

Lymph nodes Mice Paracortical high endothelial venules Oxazolone Transitory changes 

References

  1. Anderson AO, Anderson ND (1976) Lymphocyte emigration from high endothelial venules in rat lymph nodes. Immunology 31:731–748PubMedGoogle Scholar
  2. Asherson GL, Barnes RMR (1973) Contact sensitivity in the mouse. IX. The role of immunological and non-immunological inflammation in the movement of lymphocytes to immunized lymph nodes. Immunology 24:885–894PubMedGoogle Scholar
  3. Asherson GL, Pescra MACC, Thomas WR (1979) Contact sensitivity and the DNA response in mice to high and low doses of oxazolone: low dose unresponsiveness following painting and feeding and its prevention by pretreatment with cyclophosphamide. Immunology 36:449–459PubMedGoogle Scholar
  4. Cho Y, DeBruyn PPH (1979) The endothelial structure of the post-capillary venules of the lymph node and the passage of lymphocytes across the venule wall. J Ultrastruct Res 69:13–21PubMedCrossRefGoogle Scholar
  5. Claesson MH, Jørgensen O, Røpke C (1971) Light and electron microscopic studies of the paracortical post-capillary high-endothelial venules. Z Zellforsch 119:195–207PubMedCrossRefGoogle Scholar
  6. Cottier H, Turk J, Sobin L (1972) A proposal for a standardized system of reporting human lymph node morphology in relation to immunological function. Bull Wld Hlth Org 47:375–408Google Scholar
  7. Van Ewijk W, Brons NHC, Rozing J (1975) Scanning electron microscopy of homing and recirculating lymphocyte populations. Cell Immunol 19:245–261PubMedCrossRefGoogle Scholar
  8. Farr AG, De Bruyn PPH (1975) The mode of lymphocyte migration through postcapillary venule endothelium in lymph node. Am J Anat 143:59–92PubMedCrossRefGoogle Scholar
  9. Gowans JL (1959) The recirculation of lymphocytes from blood to lymph in the rat. J Physiol 146:54–69PubMedGoogle Scholar
  10. Gowans JL, Knight EJ (1964) The route of re-circulation of lymphocytes in the rat. Proc R Soc B 159:257–282CrossRefGoogle Scholar
  11. Hay JB, Hobbs BB (1977) The flow of blood to lymph nodes and its relation to lymphocyte traffic and the immune response. J Exp Med 145:31–44PubMedCrossRefGoogle Scholar
  12. Howard JC, Hunt SV, Gowans JL (1972) Identification of marrow-derived and thymus-derived small lymphocytes in the lymphoid tissue and thoracic duct lymph of normal rats. J Exp Med 135:200–219PubMedCrossRefGoogle Scholar
  13. Jørgensen O, Claesson MH (1972) Studies on the post-capillary high endothelial venules of neonatally thymectomized mice. Z Zellforsch 132:347–355PubMedGoogle Scholar
  14. Linna TJ (1970) Influence of contact allergy on thymus lymphoid cell migration. Int Arch Allergy 38:230–245PubMedGoogle Scholar
  15. Marchesi VT, Gowans JL (1964) The migration of lymphocytes through the endothelium of venules in lymph nodes: an electron microscope study. Proc R Soc B 159:283–290Google Scholar
  16. Myking AO (1979a) Dynamic and morphological responses of draining lymph nodes to single and repeated applications of oxazolone to the skin. Virchows Arch B Cell Path 31:87–102Google Scholar
  17. Myking AO (1979b) Responses of the thymus and the paracortex of draining lymph nodes to repeated applications of oxazolone to mouse skin. Virchows Arch B Cell Path 32:11–20Google Scholar
  18. Nordberg B, Rydgren L (1978) Lymphocyte migration through the walls of the post-capillary venules. Lymphology 11:211–215Google Scholar
  19. Onoé K (1976) Changes in histology of the regional lymph nodes and in the proportions of T and B cell populations by oxazolone painting or LPS injection in guinea pigs. Acta Pathol Jap 26:671–691Google Scholar
  20. Ottaway CA, Parrot DMV (1979) Regional blood flow and its relationship to lymphocyte and lymphoblast traffic during a primary immune reaction. J Exp Med 150:218–230PubMedCrossRefGoogle Scholar
  21. Syrjänen KJ (1978a) JgG in the walls of the post-capillary venules of human lymph nodes. Lymphology 11:71–74PubMedGoogle Scholar
  22. Syrjänen KJ (1978b) Post-capillary venules of the lymphatic tissues in mice with special reference to the depletion of T-lymphocyte population. Exp Mol Pathol 29:291–302PubMedCrossRefGoogle Scholar
  23. Syrjänen KJ (1978c) Post-capillary venules in the lymphatic tissues of mice bearing experimental neoplasia. Exp Pathol 15:348–354Google Scholar
  24. Syrjänen KJ (1979) Post-capillary venules in the human lymph nodes draining malignant tumours. Arch Geschwulstforsch 49:155–161PubMedGoogle Scholar
  25. Woodruff JJ, Gesner BM (1969) The effect of neuraminidase on the fate of transfused lymphocytes. J Exp Med 129:551–567PubMedCrossRefGoogle Scholar

Copyright information

© Springer-Verlag 1980

Authors and Affiliations

  • Andreas O. Myking
    • 1
  1. 1.The Gade Institute, Department of PathologyUniversity of BergenBergenNorway

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