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. 1995 Apr;48(2):M93–M100. doi: 10.1136/mp.48.2.m93

Differential expression of cell adhesion molecules in the functional compartments of lymph nodes and tonsils

R P Leite 1,2, M Carmo-Fonseca 1,2, J Cabeçadas 1,2, A Parreira 1,2, L Parreira 1,2
PMCID: PMC407932  PMID: 16695989

Abstract

Aims—To analyse the topographical distribution of adhesion molecules involved in lymphocyte recirculation in human lymph nodes and tonsils. The study focused on the expression of LECAM-1 (CD62L), VLA-α4 (CD49d), VLA-β1 (CD29), LFA-1 αL (CD11a), LFA-β2 (CD18), VCAM-1 (CD106), ICAM-1 (CD54), and H-CAM (CD44).

Methods—Reactive lymph nodes and palatine tonsils were studied using immunofluorescence methods with fluorescein isothiocyanate (FITC) labelled monoclonal antibodies directed against cell adhesion molecules. To investigate the expression patterns of these molecules in the T and B cell populations, double labelling experiments were performed using Texas Red labelled antibodies against CD2 or CD19, respectively. The images from each fluorochrome were then simultaneously analysed using a laser scanning confocal microscope.

Results—LECAM-1, VLA-α4 and H-CAM were predominantly expressed by mantle zone B cells, VCAM-1 and ICAM-1 by germinal centre cells, most of which exhibited a reticular staining pattern suggestive of follicular dendritic cells, whereas LFA-1 αL and LFA-β2 were mainly found in extrafollicular and germinal centre T cells. All high endothelial venules expressed VLA-β1 and ICAM-1, whereas VCAM-1 was present in only a few, with variable intensity.

Conclusions—The data show that all of these adhesion molecules are differentially distributed within the distinct functional microenvironments of both organs. The differences observed in the expression patterns among the B and T cells belonging to different compartments probably depend on the momentum of cell traffic, the stage of maturation/activation, as well as on their functional role in the immune response.

Keywords: Adhesion molecules

Keywords: lymphocyte recirculation

Keywords: lymph nodes

Keywords: tonsils

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Selected References

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  1. Ager A. Lymphocyte recirculation and homing: roles of adhesion molecules and chemoattractants. Trends Cell Biol. 1994 Sep;4(9):326–333. doi: 10.1016/0962-8924(94)90234-8. [DOI] [PubMed] [Google Scholar]
  2. Butcher E. C. Leukocyte-endothelial cell recognition: three (or more) steps to specificity and diversity. Cell. 1991 Dec 20;67(6):1033–1036. doi: 10.1016/0092-8674(91)90279-8. [DOI] [PubMed] [Google Scholar]
  3. Carmo-Fonseca M., Tollervey D., Pepperkok R., Barabino S. M., Merdes A., Brunner C., Zamore P. D., Green M. R., Hurt E., Lamond A. I. Mammalian nuclei contain foci which are highly enriched in components of the pre-mRNA splicing machinery. EMBO J. 1991 Jan;10(1):195–206. doi: 10.1002/j.1460-2075.1991.tb07936.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Hemler M. E. VLA proteins in the integrin family: structures, functions, and their role on leukocytes. Annu Rev Immunol. 1990;8:365–400. doi: 10.1146/annurev.iy.08.040190.002053. [DOI] [PubMed] [Google Scholar]
  5. Horst E., Meijer C. J., Radaskiewicz T., van Dongen J. J., Pieters R., Figdor C. G., Hooftman A., Pals S. T. Expression of a human homing receptor (CD44) in lymphoid malignancies and related stages of lymphoid development. Leukemia. 1990 May;4(5):383–389. [PubMed] [Google Scholar]
  6. Hynes R. O. Integrins: versatility, modulation, and signaling in cell adhesion. Cell. 1992 Apr 3;69(1):11–25. doi: 10.1016/0092-8674(92)90115-s. [DOI] [PubMed] [Google Scholar]
  7. Issekutz T. B. Lymphocyte homing to sites of inflammation. Curr Opin Immunol. 1992 Jun;4(3):287–293. doi: 10.1016/0952-7915(92)90078-s. [DOI] [PubMed] [Google Scholar]
  8. Kishimoto T. K., Jutila M. A., Butcher E. C. Identification of a human peripheral lymph node homing receptor: a rapidly down-regulated adhesion molecule. Proc Natl Acad Sci U S A. 1990 Mar;87(6):2244–2248. doi: 10.1073/pnas.87.6.2244. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Koopman G., Pals S. T. Cellular interactions in the germinal center: role of adhesion receptors and significance for the pathogenesis of AIDS and malignant lymphoma. Immunol Rev. 1992 Apr;126:21–45. doi: 10.1111/j.1600-065x.1992.tb00629.x. [DOI] [PubMed] [Google Scholar]
  10. Maio M., Del Vecchio L. Expression and functional role of CD54/Intercellular Adhesion Molecule-1 (ICAM-1) on human blood cells. Leuk Lymphoma. 1992 Sep;8(1-2):23–33. doi: 10.3109/10428199209049814. [DOI] [PubMed] [Google Scholar]
  11. Möller P., Eichelmann A., Koretz K., Mechtersheimer G. Adhesion molecules VLA-1 to VLA-6 define discrete stages of peripheral B lymphocyte development and characterize different types of B cell neoplasia. Leukemia. 1992 Apr;6(4):256–264. [PubMed] [Google Scholar]
  12. Pals S. T., Horst E., Scheper R. J., Meijer C. J. Mechanisms of human lymphocyte migration and their role in the pathogenesis of disease. Immunol Rev. 1989 Apr;108:111–133. doi: 10.1111/j.1600-065x.1989.tb00015.x. [DOI] [PubMed] [Google Scholar]
  13. Picker L. J., Butcher E. C. Physiological and molecular mechanisms of lymphocyte homing. Annu Rev Immunol. 1992;10:561–591. doi: 10.1146/annurev.iy.10.040192.003021. [DOI] [PubMed] [Google Scholar]
  14. Picker L. J., Treer J. R., Ferguson-Darnell B., Collins P. A., Buck D., Terstappen L. W. Control of lymphocyte recirculation in man. I. Differential regulation of the peripheral lymph node homing receptor L-selectin on T cells during the virgin to memory cell transition. J Immunol. 1993 Feb 1;150(3):1105–1121. [PubMed] [Google Scholar]
  15. Pinto A., Gattei V., Soligo D., Parravicini C., Del Vecchio L. New molecules burst at the leukocyte surface. A comprehensive review based on the 15th International Workshop on Leukocyte Differentiation Antigens. Boston, USA, 3-7 November, 1993. Leukemia. 1994 Mar;8(3):347–358. [PubMed] [Google Scholar]
  16. Rouse R. V., Reichert R. A., Gallatin W. M., Weissman I. L., Butcher E. C. Localization of lymphocyte subpopulations in peripheral lymphoid organs: directed lymphocyte migration and segregation into specific microenvironments. Am J Anat. 1984 Jul;170(3):391–405. doi: 10.1002/aja.1001700313. [DOI] [PubMed] [Google Scholar]
  17. Shimizu Y., Newman W., Tanaka Y., Shaw S. Lymphocyte interactions with endothelial cells. Immunol Today. 1992 Mar;13(3):106–112. doi: 10.1016/0167-5699(92)90151-V. [DOI] [PubMed] [Google Scholar]
  18. Shimizu Y., Shaw S. Lymphocyte interactions with extracellular matrix. FASEB J. 1991 Jun;5(9):2292–2299. doi: 10.1096/fasebj.5.9.1860621. [DOI] [PubMed] [Google Scholar]
  19. Sprent J. T and B memory cells. Cell. 1994 Jan 28;76(2):315–322. doi: 10.1016/0092-8674(94)90338-7. [DOI] [PubMed] [Google Scholar]
  20. Springer T. A. Adhesion receptors of the immune system. Nature. 1990 Aug 2;346(6283):425–434. doi: 10.1038/346425a0. [DOI] [PubMed] [Google Scholar]
  21. Springer T. A., Dustin M. L., Kishimoto T. K., Marlin S. D. The lymphocyte function-associated LFA-1, CD2, and LFA-3 molecules: cell adhesion receptors of the immune system. Annu Rev Immunol. 1987;5:223–252. doi: 10.1146/annurev.iy.05.040187.001255. [DOI] [PubMed] [Google Scholar]
  22. Springer T. A. Traffic signals for lymphocyte recirculation and leukocyte emigration: the multistep paradigm. Cell. 1994 Jan 28;76(2):301–314. doi: 10.1016/0092-8674(94)90337-9. [DOI] [PubMed] [Google Scholar]
  23. Stein H., Gerdes J., Mason D. Y. The normal and malignant germinal centre. Clin Haematol. 1982 Oct;11(3):531–559. [PubMed] [Google Scholar]
  24. Zutter M. M. Immunolocalization of integrin receptors in normal lymphoid tissues. Blood. 1991 May 15;77(10):2231–2236. [PubMed] [Google Scholar]
  25. van der Valk P., Meijer C. J. The histology of reactive lymph nodes. Am J Surg Pathol. 1987 Nov;11(11):866–882. doi: 10.1097/00000478-198711000-00005. [DOI] [PubMed] [Google Scholar]

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