CD151 interacts with integrin beta 2 in B cell lymphomas

  • Philipp M. Hagemann
  • , Angelique N. Kenyon
  • , Alfredo Cabrera-Orefice
  • , Abbey B. Arp
  • , Eva A. M. Hesius
  • , Michiel van den Brand
  • , Sjoerd J. van Deventer
  • , Daphne de Jong
  • , Blanca Scheijen
  • , Zijun Y. Xu-Monette
  • , Ulrich Brandt
  • , Cornelia G. Spruijt
  • , Michiel Vermeulen
  • , Martin ter Beest
  • , Ken H. Young
  • , Annemiek B. van Spriel*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

CD151 is a broadly expressed four-transmembrane protein (tetraspanin) that interacts with laminin‐binding integrins like integrin alpha 3 (ITGA3). CD151 drives tumor development and expression correlates with poor prognosis in solid cancers, but CD151 has not been studied in B cell malignancies. We investigated CD151 expression on normal human B cells and B cell lymphomas using highly sensitive flow cytometry and immunohistochemistry. Expression of CD151 increased during B cell differentiation from naïve to memory B cells to plasma cells. B lymphoma cell lines and human lymphoma biopsy samples expressed higher levels of CD151 compared to normal B cells, but CD151‐deficient lymphomas were identified as well. To investigate the function of CD151 in B cells, CD151‐deficient and stably transduced CD151 expressing B lymphoma cell lines were generated. Immunoprecipitation-mass spectrometry analysis of CD151 protein complexes identified integrin beta 2 (ITGB2) as new interaction partner in lymphoma cells. Deficiency of CD151 decreased cell surface expression of alpha integrin subunits L (ITGAL) and M (ITGAM), and impaired ICAM-1-mediated cell spreading. Interestingly, B cells and lymphomas did not express ITGA3‐bound CD151 compared to T cells that expressed two different populations of integrin‐bound and integrin‐free CD151. Despite CD151 expression not being related to clinical outcome of patients with diffuse large B cell lymphoma (DLBCL), CD151 expression was predominantly detected in the activated (ABC) subset of DLBCL. Taken together, we identified a new molecular association of CD151 with ITGB2, and targeting integrin-free CD151 in DLBCL may represent a new target for immunotherapy.
Original languageEnglish
Article number221
JournalCellular and molecular life sciences
Volume82
Issue number1
DOIs
Publication statusPublished - 1 Dec 2025

Keywords

  • CD18
  • Cell spreading
  • Membrane protein
  • Non-Hodgkin lymphoma
  • TSPAN24

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