Plećas-Solarović B, Hristić-Zivković I, Radojević K, Kosec D, Leposavić G
Department of Physiology, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11221 Belgrade, Serbia and Montenegro.
Histol Histopathol. 2005 Jul;20(3):833-41. doi: 10.14670/HH-20.833.
In order to examine the influence of chronic alpha1-adrenergic receptor (alpha1-AR) blockade on the thymus structure and T-cell maturation, peripubertal and adult male rats were treated with urapidil (0.20 mg/kg BW/d; s.c.) over 15 consecutive days. Thymic structure and phenotypic characteristics of the thymocytes were assessed by stereological and flow cytometry analysis, respectively. In immature rats, treatment with urapidil reduced the body weight gain and, affecting the volume of cortical compartment and its cellularity decreased the organ size and the total number of thymocytes compared to age-matched saline-injected controls. The percentage of CD4+8- single positive (SP) thymocytes was decreased, while that of CD4-8+ was increased suggesting, most likely, a disregulation in final steps of the positively selected cells maturation. However, alpha1-AR blockade in adult rats increased the thymus weight as a consequence of increase in the cortical size and cellularity. The increased percentage of most immature CD4-8- double negative (DN) cells associated with decreased percentage of immature CD4+8+ double positive (DP) thymocytes suggests a decelerated transition from DN to DP stage of T-cell development. As in immature rats, the treatment in adult rats evoked changes in the relative numbers of SP cells, but contrary to immature animals, favoring the maturation of CD4+8- over CD4-8+ thymocytes. These results demonstrate that: i) chronic blockade of alpha1-ARs affects both the thymus structure and thymocyte differentiation, ii) these effects are age-dependent, pointing out to pharmacological manipulation of alpha1-AR-mediated signaling as potential means for modulation of the intrathymic T-cell maturation.
为了研究慢性α1-肾上腺素能受体(α1-AR)阻断对胸腺结构和T细胞成熟的影响,对青春期前和成年雄性大鼠连续15天皮下注射乌拉地尔(0.20 mg/kg体重/天)。分别通过体视学和流式细胞术分析评估胸腺结构和胸腺细胞的表型特征。在未成熟大鼠中,与年龄匹配的注射生理盐水的对照组相比,乌拉地尔治疗降低了体重增加,并影响皮质区室的体积及其细胞数量,从而减小了器官大小和胸腺细胞总数。CD4+8-单阳性(SP)胸腺细胞的百分比降低,而CD4-8+的百分比增加,这很可能表明阳性选择细胞成熟的最后步骤出现失调。然而,成年大鼠中的α1-AR阻断由于皮质大小和细胞数量增加而使胸腺重量增加。最不成熟的CD4-8-双阴性(DN)细胞百分比增加,同时未成熟的CD4+8+双阳性(DP)胸腺细胞百分比降低,这表明T细胞发育从DN期到DP期的转变减速。与未成熟大鼠一样,成年大鼠的治疗引起了SP细胞相对数量的变化,但与未成熟动物相反,有利于CD4+8-胸腺细胞而非CD4-8+胸腺细胞的成熟。这些结果表明:i)α1-ARs的慢性阻断影响胸腺结构和胸腺细胞分化,ii)这些影响具有年龄依赖性,指出α1-AR介导的信号传导的药理学操纵是调节胸腺内T细胞成熟的潜在手段。