Skip to main content

Functional Involvement of CD44, a Family of Cell Adhesion Molecules, in Immune Responses, Tumour Progression and Haematopoiesis

  • Chapter
Gene Therapy of Cancer

Abstract

Cell-cell and cell-extracellular matrix (ECM) interactions play fundamental roles in many biological processes. Cells adhere to the ECM and to each other via specific cell surface receptors such as the selectins, integrins, Cadherins, members of the immunoglobulin superfamily, and of the CD44 superfamily [1]. Surface molecules are necessary for cellular cross-talking and thus have a major impact on gene regulation, immune surveillance, immunological memory, motility, differentiation and growth control. Defined alterations in the cellular communication are features of embryonic development, immunobiology and neoplastic transformation. The model molecule and its functional analysis described here is the glycoprotein CD44 and its many isoforms [2]. CD44 has been implicated to act in processes such as lymphocyte homing, haematopoiesis, tumour dissemination, lymphocyte activation, pattern formation in embryogenesis and inflammatory reactions [2–5]. This multipurpose nature of CD44 can possibly be explained by the enormous number of isoforms. Although only encoded by one gene, CD44 represents a large family of molecules which differ in the primary structure. These differences are brought about by alternative splicing of at least ten unique exons, encoding extracellular regions. The function of the variant isoforms has been a matter of speculation for a long time, but now analysing mice which carry targeted mutations of specific exons a clearer picture is emerging.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 259.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 329.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 329.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Ruiz, P., Günthert, U., 1996: The cellular basis of metastasis. World J. Urol. 14, 141–150.

    Article  PubMed  CAS  Google Scholar 

  2. Günthert, U., 1996: CD44 in malignant disorders. Current Topics Microbiol. Immunol. 213-I: 271–285. Editors U. Günthert, W. Birchmeier and P.M. Schlag of Vol. 213 I, II, III: Attempts to understand metastasis formation. Springer, Heidelberg.

    Google Scholar 

  3. Stauder, R., Günthert, U., 1995: CD44 isoforms-impact on lymphocyte activation and differentiation. The Immunologist 3, 78–83.

    CAS  Google Scholar 

  4. Ruiz, P., Schwärzler, C., Günthert, U., 1995: CD44 isoforms during differentiation and development. BioEssays 17, 17–24.

    Article  PubMed  CAS  Google Scholar 

  5. Günthert, U., Stauder, R., Mayer, B., Terpe, H.-J., Finke, L., Friedrichs, K., 1995: Are CD44 variant isoforms involved in human tumour progression? Cancer Surveys 24, 19–42.

    PubMed  Google Scholar 

  6. Rosenberg, W.M.C., Prince, C., Kaklamanis, L., Fox, S.B., Jackson, D.G., Simmons, D.L., Chapman, R.W., Trowell, J.M., Jewell, D.P., Bell, J.I., 1995: Increased expression of CD44v6 and CD44v3 in ulcerative colitis but not colonic Crohn’s disease. Lancet 345, 1205–1209.

    Article  PubMed  CAS  Google Scholar 

  7. Neurath, M.F., Fuss, I., Kelsall, B.L., Stüber, E.R., Strober, W., 1995: Antibodies to IL-12 abrogate established experimental colitis in mice. J. Exp. Med. 182, 1281–1290.

    Article  PubMed  CAS  Google Scholar 

  8. Wittig, B., Seiter, S., Föger, N., Schwärzler, C., Günthert, U., Zöller, M., 1997: Functional activity of murine CD44 variant isoforms in allergic and delayed type hypersensitivity. Immunol. Lett. 57: 217–223.

    Article  PubMed  CAS  Google Scholar 

  9. Powrie, F., 1995: T cells in inflammatory bowel disease: protective and pathogenic roles. Immunity 3, 171–174.

    Article  PubMed  CAS  Google Scholar 

  10. Gerritse, K., Laman, J.D., Noelle, R.J., Aruffo, A., Ledbetter, J.A., Boersma, W.J.A., Claassen, E., 1996: CD40-CD40 ligand interactions in experimental allergic encephalomyelitis and multiple sclerosis. Proc. Natl. Acad. Sci. USA 93, 2499–2504.

    Article  PubMed  CAS  Google Scholar 

  11. Mikecz, K., Brennan, F.R., Kim, J.H., Giant, T.T., 1995: Anti-CD44 treatment abrogates tissue oedema and leukocyte infiltration in murine arthritis. Nature Med. 1, 558–563.

    Article  PubMed  CAS  Google Scholar 

  12. Dzierzak, E., Medvinsky, A., 1995: Mouse embryonic hematopoiesis. TIG 11, 359–366.

    Article  PubMed  CAS  Google Scholar 

  13. Zuniga-Pflücker, J.C., Lenardo, M., 1996: Regulation of thymocyte development from immature progenitors. Curr. Opin. Immunol. 8, 215–224.

    Article  PubMed  Google Scholar 

  14. Wu, L., Kincade, P.W., Shortman K., 1993: The CD44 expressed on the earliest intrathymic precursors population functions as a thymus homing molecule but does not bind to hyaluronate. Immunol. Letters 38, 69–75.

    Article  CAS  Google Scholar 

  15. Rolink, A., Andersson, J., Ghia, P., Grawunder, U., Haasner, D., Karasuyama, H., ten Boekel, E., Winkler, T.H., Melchers, F., 1995: B-cell development in mouse and men. Immunologist 3/4, 125–128.

    CAS  Google Scholar 

  16. Stauder, R., Eisterer, A., Thaler, J., Günthert, U., 1995: CD44 variant isoforms in non-Hodgkin’s lymphoma: A new independent prognostic factor. Blood 85, 2885–2899.

    PubMed  CAS  Google Scholar 

  17. Stauder, R., Van Driel, M., Schwärzler, C., Thaler, J., Lokhorst, H.M., Kreuser, E.D., Bloem, A.C., Günthert, U., Eisterer, W., 1996: Different CD44 splicing patterns define prognostic subgroups in multiple myeloma. Blood 88: 3101–3108.

    PubMed  CAS  Google Scholar 

  18. Gossen, M., Freundlieb, S., Bender, G., Müller, G., Hillen, W., Bujard, H., 1995: Transcriptional activation by tetracyclines in mammalian cells. Science 268, 1766–1769.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1998 Springer Science+Business Media New York

About this chapter

Cite this chapter

Günthert, U. et al. (1998). Functional Involvement of CD44, a Family of Cell Adhesion Molecules, in Immune Responses, Tumour Progression and Haematopoiesis. In: Walden, P., Trefzer, U., Sterry, W., Farzaneh, F., Zambon, P. (eds) Gene Therapy of Cancer. Advances in Experimental Medicine and Biology, vol 451. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-5357-1_7

Download citation

  • DOI: https://doi.org/10.1007/978-1-4615-5357-1_7

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4613-7444-2

  • Online ISBN: 978-1-4615-5357-1

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics