Kawana Satoshi, Suzuki Osamu, Hashimoto Yuko
Department of Diagnostic Pathology, School of Medicine, Fukushima Medical University, Fukushima city, Japan.
J Clin Exp Hematop. 2024 Dec 25;64(4):275-285. doi: 10.3960/jslrt.23002. Epub 2024 Nov 28.
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.
分化簇54(CD54),也称为细胞间黏附分子-1(ICAM-1),是一种属于免疫球蛋白超家族的跨膜糖蛋白。尽管已表明CD54参与B细胞淋巴瘤细胞系的细胞间黏附和增殖,但其表达的临床意义尚未阐明。我们分析了40例伴有血管侵犯的弥漫性大B细胞淋巴瘤(DLBCL)病例中的Ki-67指数、CD54及其受体(CD11a)的表达状态以及肿瘤细胞的细胞间距离,以分析细胞黏附与增殖状态之间的关联。在14例(35%)病例的血管外/血管内肿瘤细胞中,CD54和CD11a同时表达(双阳性)。组织学上,双阳性病例的淋巴瘤细胞在血管外肿瘤细胞中的Ki-67指数显著高于血管内肿瘤细胞,而非双阳性病例的淋巴瘤细胞则未观察到差异。与血管内细胞间距离相比,血管外细胞间距离显著缩短,提示CD54介导的细胞间黏附与细胞增殖之间存在关联。我们进一步证实,重组LFA1(CD11a/CD18)处理可使源自人DLBCL的细胞系HBL-2黏附于LFA1并提高细胞活力。这些发现表明,通过CD54的细胞间黏附维持了一部分DLBCL的细胞增殖活性。本研究为进一步开展研究以确定细胞间相关和非黏附依赖性细胞增殖的详细机制提供了有价值的基础。