Wake A, Tanaka Y, Nakatsuka K, Misago M, Oda S, Morimoto I, Eto S
First Department of Internal Medicine, University of Occupational and Environmental Health, School of Medicine, Kitakyushu, Japan.
Blood. 1995 Sep 15;86(6):2257-67.
Adult T-cell leukemia (ATL) is a human T-cell leukemia virus type I (HTLV-I)-infected lymphoproliferative disorder that shows a characteristic nodular infiltration into various tissues, hypercalcemia, and subsequent rapid increase of peripheral ATL cell number. ATL cells and HTLV-I-infected T-cell lines also make cluster formation rapidly after the non-stimulative culture. However, the mechanism of the acute proliferation of ATL cells remains to be understood. We report the following novel features of homotypic adhesion via leukocyte function-associated antigen-1 (LFA-1)/intracellular adhesion molecule-1 (ICAM-1) pathway that suggest a role for it in cytokine production and rapid proliferation of ATL cells: (1) ATL cells show clustering in a calcium dependent manner, even at the higher concentration; (2) ATL cells consistently and highly express ICAM-1 and an active form of LFA-1, whereas integrin expression, except for LFA-1, is rather lower compared with that of normal CD4+ T cells; (3) ATL cells make conjugate formation within 6 minutes and clustering within 48 hours, both of which are inhibited by the addition of monoclonal antibodies (MoAbs) against LFA-1 and ICAM-1; (4) spontaneous mRNA transcription and protein secretion of both interleukin-1 and parathyroid hormone-related protein are observed consistently in ATL cells, and these productions are inhibited by anti-LFA-1 and anti-ICAM-1 MoAbs but are markedly increased by cross-linking of LFA-1 and ICAM-1 by the immobilized specific MoAbs; and (5) proliferative responses of ATL cells are also inhibited by these MoAbs. We propose that ATL cells proliferate in sequential events: the homotypic and calcium-dependent adhesion through LFA-1/ICAM-1, the signal transduction through these adhesion molecules, the production of cytokines, and the proliferation.
成人T细胞白血病(ATL)是一种由I型人类T细胞白血病病毒(HTLV-I)感染引起的淋巴细胞增殖性疾病,其特征为向各种组织的结节状浸润、高钙血症以及外周血ATL细胞数量随后的快速增加。ATL细胞和HTLV-I感染的T细胞系在非刺激培养后也能迅速形成聚集。然而,ATL细胞急性增殖的机制仍有待阐明。我们报告了通过白细胞功能相关抗原-1(LFA-1)/细胞间黏附分子-1(ICAM-1)途径的同型黏附的以下新特征,这些特征提示其在ATL细胞细胞因子产生和快速增殖中起作用:(1)即使在较高浓度下,ATL细胞也以钙依赖的方式聚集;(2)ATL细胞持续且高度表达ICAM-1和活性形式的LFA-1,而除LFA-1外的整合素表达与正常CD4+T细胞相比相对较低;(3)ATL细胞在6分钟内形成共轭并在48小时内聚集,这两者均被添加抗LFA-1和抗ICAM-1单克隆抗体(MoAbs)所抑制;(4)在ATL细胞中持续观察到白细胞介素-1和甲状旁腺激素相关蛋白的自发mRNA转录和蛋白分泌,并且这些产物被抗LFA-1和抗ICAM-1 MoAbs抑制,但通过固定化特异性MoAbs使LFA-1和ICAM-1交联则显著增加;(5)这些MoAbs也抑制ATL细胞的增殖反应。我们提出ATL细胞通过以下连续事件增殖:通过LFA-1/ICAM-1的同型和钙依赖黏附、通过这些黏附分子的信号转导、细胞因子的产生以及增殖。