Houssami R, Check I J, Hunter R L
Department of Pathology, Emory University, Atlanta, Georgia 30322.
Proc Soc Exp Biol Med. 1990 Jul;194(3):274-82. doi: 10.3181/00379727-194-43091.
T150R1, an 8000-dalton copolymer with sodium ionophore activity, has been shown to modulate cellular responses in multiple systems. In this article, we studied its effects on lymphoid and hematopoietic organs in the context of the adrenal-pituitary axis. When injected in mice as an oil in water emulsion, T150R1 caused a rapid, profound, and dose-dependent thymic involution accompanied by splenic hyperplasia. Time course experiments with a 2.5-mg dose revealed that the thymus size was minimal at Day 2, rose to normal by Day 14, then enlarged and gradually returned to normal by Week 6 postinjection. Thymic involution was due to cellular depletion of the cortical area, whereas thymic enlargement was due to cortical hyperplasia. Splenomegaly was seen as early as Day 4, peaked by Day 14, and gradually returned to normal by Week 6. The splenic enlargement was due to hyperplasia of the red pulp, with evidence of proliferating erythropoietic, myelopoietic, and megakaryopoietic precursors. In addition, the bone marrow was stimulated and extramedullary hematopoiesis was present in the liver. The effects of T150R1 on the thymus appeared to be mediated by corticosteroids while the effects on hematopoiesis were not. Corticosterone and ACTH levels were increased in treated animals. Adrenalectomy diminished the T150R1-induced thymic involution but enhanced the splenic hyperplasia. Hypophysectomy did not prevent thymic involution, suggesting that T150R1 has endocrine stimulatory effects. These data suggest that T150R1 represents a new class of ionophores which may act on excitable cells within the endocrine, immune, and hematopoietic systems.
T150R1是一种具有钠离子载体活性的8000道尔顿共聚物,已被证明可调节多种系统中的细胞反应。在本文中,我们在肾上腺 - 垂体轴的背景下研究了其对淋巴和造血器官的影响。当以水包油乳剂形式注射到小鼠体内时,T150R1会引起快速、显著且剂量依赖性的胸腺退化,并伴有脾脏增生。用2.5毫克剂量进行的时间进程实验表明,胸腺大小在第2天最小,到第14天恢复正常,然后在注射后第6周时增大并逐渐恢复正常。胸腺退化是由于皮质区域的细胞耗竭,而胸腺增大是由于皮质增生。脾脏肿大最早在第4天出现,在第14天达到峰值,并在第6周时逐渐恢复正常。脾脏肿大是由于红髓增生,有红细胞生成、骨髓生成和巨核细胞生成前体增殖的证据。此外,骨髓受到刺激,肝脏中出现髓外造血。T150R1对胸腺的作用似乎是由皮质类固醇介导的,而对造血的作用则不是。治疗动物的皮质酮和促肾上腺皮质激素水平升高。肾上腺切除术减轻了T150R1诱导的胸腺退化,但增强了脾脏增生。垂体切除术并不能阻止胸腺退化,这表明T150R1具有内分泌刺激作用。这些数据表明,T150R1代表了一类新型离子载体,可能作用于内分泌、免疫和造血系统中的可兴奋细胞。