Katz I R, Asofsky R, Thorbecke G J
J Immunol. 1980 Sep;125(3):1355-9.
The cellular origin of reticulum cell sarcoma (RCS) in SJL/J mice was studied by comparing the incidence of spontaneous RCS in control mice and in mice suppressed with goat anti-mu Ig from birth on. At 10 months of age anti-mu suppressed mice had 0% RCS as opposed to 60% in control mice. Growth of two i.v. injected transplantable RCS lines in anti-mu suppressed mice was approximately 60% as compared with growth in normal SJL/J mice. Proliferative responses of thymus and lymph node cells from anti-mu suppressed mice to RCS, mitomycin-treated syngeneic spleen cells (M. Spl.) Con A, and PHA were entirely normal. However, M. Spl. from anti-mu suppressed mice caused minimal or no stimulation of T cells from normal or anti-mu suppressed responders. The results suggest that the normal syngeneic stimulator cell is of B cell origin, either representing a direct precursor of RCS or indirectly influencing RCS appearance. A B cell origin of RCS is, furthermore, in agreement with some of its characteristics, such as surface markers (Ia antigens, Ly b) and in vivo localization properties.
通过比较对照小鼠和从出生起就用山羊抗μ Ig抑制的小鼠中自发性网状细胞肉瘤(RCS)的发生率,研究了SJL/J小鼠中网状细胞肉瘤的细胞起源。10个月大时,抗μ抑制的小鼠RCS发生率为0%,而对照小鼠为60%。与正常SJL/J小鼠相比,两种静脉注射的可移植RCS细胞系在抗μ抑制的小鼠中的生长约为60%。抗μ抑制小鼠的胸腺和淋巴结细胞对RCS、丝裂霉素处理的同基因脾细胞(M. Spl.)、刀豆蛋白A和植物血凝素的增殖反应完全正常。然而,抗μ抑制小鼠的M. Spl.对正常或抗μ抑制应答者的T细胞刺激最小或无刺激。结果表明,正常的同基因刺激细胞起源于B细胞,要么代表RCS的直接前体,要么间接影响RCS的出现。此外,RCS的B细胞起源与其一些特征相符,如表面标志物(Ia抗原、Ly b)和体内定位特性。