Wiktor-Jedrzejczek W, Szczylik C, Gornas P, Ahmed A, Sharkis S J, Siekierzyński M
Exp Hematol. 1981 Jan;9(1):22-31.
Seeking a system with which to study the antitheta-sensitive regulatory cell (TSRC), other than the W/Wv anemic mouse, we tested a model which utilizes mouse strains differing almost exclusively in theta allotype. AKR/FuRd Thy 1.1 mice were immunized against CBA Thy 1.2 mouse thymocytes to produce antibody. The immunized mice were lethally irradiated and grafted with marrow cells from AKR/Cum Thy 1.2 mice. It was reasoned that in this situation antitheta-sensitive cells present in or produced by the graft will be destroyed, while theta-incompatible host cells may not be as capable of collaboration with the graft stem cells as are the graft's theta-compatible cells. Anti-Thy 1.2 immunization did not influence the number of spleen colonies formed by marrow from Thy 1.2 mice; but the colonies formed, especially the erythropoietic colonies, were reduced in size. Also, both the relative and absolute frequencies of erythropoietic colonies were decreased, while those of granulopoietic colonies were increased. Therefore, the destruction of antitheta-sensitive cells in this system resulted in decreased effectiveness of spleen colony growth and altered the differentiation pattern of colony-forming cells. These effects were not observed in control groups immunized with CBA tissues not bearing the Thy 1.2 antigen. This study further stresses the importance of the theta antigen in hemopoietic differentiation and may provide an alternative in vivo model for studying the TSRC.
为了寻找一种除W/Wv贫血小鼠外用于研究抗θ敏感调节细胞(TSRC)的系统,我们测试了一种模型,该模型利用几乎仅在θ同种异型上存在差异的小鼠品系。用CBA Thy 1.2小鼠胸腺细胞免疫AKR/FuRd Thy 1.1小鼠以产生抗体。对免疫后的小鼠进行致死性照射,然后移植来自AKR/Cum Thy 1.2小鼠的骨髓细胞。据推测,在这种情况下,移植物中存在的或由移植物产生的抗θ敏感细胞将被破坏,而θ不相容的宿主细胞与移植物干细胞协作的能力可能不如移植物中θ相容的细胞。抗Thy 1.2免疫不影响Thy 1.2小鼠骨髓形成的脾集落数量;但形成的集落,尤其是红细胞生成集落,大小减小。此外,红细胞生成集落的相对频率和绝对频率均降低,而粒细胞生成集落的频率增加。因此,该系统中抗θ敏感细胞的破坏导致脾集落生长效率降低,并改变了集落形成细胞的分化模式。在用不携带Thy 1.2抗原的CBA组织免疫的对照组中未观察到这些效应。这项研究进一步强调了θ抗原在造血分化中的重要性,并可能为研究TSRC提供一种替代的体内模型。