Wei Li Xin, Zhou Jian Nian, Roberts Arthur I, Shi Yu Fang
Department of Molecular Genetics, Microbiology and Immunology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, 661 Hoes Lane, Piscataway, New Jersey 08854, USA.
Cell Res. 2003 Dec;13(6):465-71. doi: 10.1038/sj.cr.7290189.
Hindlimb unloading (HU) in rodent is a well-accepted ground-based model used to simulate some of the conditions of space flight and reproduce its deleterious effects on the musculoskeletal, cardiovascular and immune systems. In this study, the effects of HU on lymphocyte homeostasis in the spleen and thymus of mice were examined. HU was found to drastically deplete various cell populations in the spleen and thymus. These changes are likely to be mediated by apoptosis, since DNA strand breaks indicative of apoptosis were detected by terminal deoxynucleotidyl transferase-mediated nick end-labeling in both splenocytes and thymocytes. Surprisingly, administration of opioid antagonists or interference with the Fas-FasL interaction was able to block HU-induced reductions of splenocytes, but not thymocytes. On the other hand, steroid receptor antagonists blocked the reduction of lymphocyte numbers in both spleen and thymus. Therefore, the effects of HU on the homeostasis of splenocytes and thymocytes must be exerted through distinct mechanisms.
啮齿动物后肢卸载(HU)是一种广泛认可的地面模型,用于模拟太空飞行的某些条件,并重现其对肌肉骨骼、心血管和免疫系统的有害影响。在本研究中,检测了HU对小鼠脾脏和胸腺中淋巴细胞稳态的影响。发现HU会大幅减少脾脏和胸腺中的各种细胞群。这些变化可能是由细胞凋亡介导的,因为通过末端脱氧核苷酸转移酶介导的缺口末端标记在脾细胞和胸腺细胞中均检测到了指示细胞凋亡的DNA链断裂。令人惊讶的是,给予阿片类拮抗剂或干扰Fas-FasL相互作用能够阻止HU诱导的脾细胞减少,但不能阻止胸腺细胞减少。另一方面,类固醇受体拮抗剂可阻止脾脏和胸腺中淋巴细胞数量的减少。因此,HU对脾细胞和胸腺细胞稳态的影响必定是通过不同机制发挥作用的。