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Updated: Jun 6, 2025

Murine Model of CD40-activation of B cells
Published on: March 5, 2010
Cell-to-cell adhesion via CD54 (intercellular adhesion molecule-1)-associated cell proliferation in diffuse large
Satoshi Kawana1, Osamu Suzuki1, Yuko Hashimoto1
1Department of Diagnostic Pathology, School of Medicine, Fukushima Medical University, Fukushima city, Japan.
Insights
Cluster of Differentiation 54 (CD54), or ICAM-1, promotes cell adhesion and proliferation in diffuse large B-cell lymphoma (DLBCL). This adhesion via CD54 sustains DLBCL cell growth, suggesting therapeutic potential.
Area of Science:
- Immunology
- Oncology
- Cell Biology
Background:
- Cluster of Differentiation 54 (CD54), also known as intracellular adhesion molecule-1 (ICAM-1), is an immunoglobulin superfamily member.
- CD54's role in B-cell lymphoma proliferation and adhesion requires further clinical elucidation.
- Understanding CD54's function is crucial for diffuse large B-cell lymphoma (DLBCL) research.
Purpose of the Study:
- To analyze the association between cell adhesion and proliferation in DLBCL.
- To investigate the clinical significance of CD54 and its receptor CD11a expression in DLBCL with vascular invasion.
- To explore the mechanism of CD54-mediated cell-cell adhesion in DLBCL proliferation.
Main Methods:
- Analysis of Ki-67 indices, CD54, and CD11a expression in 40 DLBCL cases.
- Assessment of intercellular distance in extra/intravascular tumor cells.
- In vitro study using DLBCL cell line HBL-2 treated with recombinant LFA1 (CD11a/CD18).
Main Results:
- CD54 and CD11a co-expression (double-positive) observed in 35% of DLBCL cases.
- Double-positive cases showed higher Ki-67 indices in extravascular tumor cells, indicating increased proliferation.
- Shorter intercellular distances in extravascular tumor cells suggest CD54-mediated adhesion promotes proliferation.
- Recombinant LFA1 treatment increased HBL-2 cell adhesion and viability.
Conclusions:
- CD54-mediated cell-to-cell adhesion sustains the proliferative activity in a subset of DLBCL.
- These findings highlight a potential mechanism linking cell adhesion and proliferation in DLBCL.
- Further research is warranted to detail CD54's role in DLBCL cell proliferation.
Abstract:
Cluster of Differentiation 54 (CD54), also known as intracellular adhesion molecule-1 (ICAM-1), is a transmembrane glycoprotein belonging to the immunoglobulin superfamily. Although CD54 has been shown to be involved in cell-to-cell adhesion and proliferation of B-cell lymphoma cell lines, the clinical significance of its expression has not yet been elucidated. We analyzed Ki-67 indices, the expression status of CD54 and its receptor (CD11a), and the intercellular distance of tumor cells in 40 diffuse large B-cell lymphoma (DLBCL) cases with vascular invasion to analyze the association of cell adhesion and proliferation status. CD54 and CD11a were simultaneously expressed (double-positive) in extra/intravascular tumor cells in 14 (35%) of the cases. Histologically, lymphoma cells of the double positive cases exhibited significantly higher Ki-67 index in extravascular tumor cells than that in the intravascular ones, while no difference was observed in lymphoma cells of the non-double positive cases. The significantly shorter extravascular intercellular distance compared with the intravascular intercellular distance suggested the association between cell-cell adhesion mediated by CD54 and cell proliferation. We further confirmed that the treatment of the recombinant LFA1 (CD11a/CD18) showed the adhesion of human DLBCL-derived cell line HBL-2 to LFA1 and increased cell viability. These findings suggest that cell-to-cell adhesion via CD54 maintains the cell proliferative activity of a subset of DLBCL. This study provides a valuable foundation upon which further research may be conducted to determine detailed mechanisms of cell-to-cell-associated and adhesion-independent cell proliferation.
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