弥漫大 B 细胞淋巴瘤病例中细胞间通过 CD54(细胞间粘附分子-1)的粘附与细胞增殖有关。

IF 0.9 Q4 HEMATOLOGY
Satoshi Kawana, Osamu Suzuki, Yuko Hashimoto
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引用次数: 0

摘要

分化簇 54(CD54)又称细胞内粘附分子-1(ICAM-1),是一种跨膜糖蛋白,属于免疫球蛋白超家族。虽然 CD54 已被证明参与了 B 细胞淋巴瘤细胞系的细胞间粘附和增殖,但其表达的临床意义尚未阐明。我们分析了40例有血管侵犯的弥漫大B细胞淋巴瘤(DLBCL)病例的Ki-67指数、CD54及其受体(CD11a)的表达状态和肿瘤细胞的细胞间距离,以分析细胞粘附和增殖状态的关联。14例(35%)病例的血管外/血管内肿瘤细胞同时表达了CD54和CD11a(双阳性)。从组织学角度看,双阳性病例中血管外肿瘤细胞的 Ki-67 指数明显高于血管内肿瘤细胞,而非双阳性病例的淋巴瘤细胞则无差异。与血管内细胞间距离相比,血管外细胞间距离明显缩短,这表明 CD54 介导的细胞-细胞粘附与细胞增殖之间存在关联。我们进一步证实,用重组 LFA1(CD11a/CD18)处理后,人 DLBCL 衍生细胞系 HBL-2 能粘附到 LFA1 上,并提高细胞活力。这些发现表明,通过 CD54 进行的细胞间粘附维持了 DLBCL 亚群的细胞增殖活性。这项研究提供了一个宝贵的基础,可在此基础上开展进一步研究,以确定细胞间相关和粘附无关的细胞增殖的详细机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cell-to-cell adhesion via CD54 (intercellular adhesion molecule-1)-associated cell proliferation in diffuse large B-cell lymphoma cases.

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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来源期刊
CiteScore
2.00
自引率
6.70%
发文量
25
审稿时长
11 weeks
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