Miyakawa Yoshitaka, Ohnishi Yasuyuki, Tomisawa Masashi, Monnai Makoto, Kohmura Kanoko, Ueyama Yoshito, Ito Mamoru, Ikeda Yasuo, Kizaki Masahiro, Nakamura Masato
Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Biochem Biophys Res Commun. 2004 Jan 9;313(2):258-62. doi: 10.1016/j.bbrc.2003.11.120.
We developed a new experimental animal model of human multiple myeloma using immunodeficient NOD/SCID/gammac(null) (NOG) mice. A human myeloma cell line, U266, was intravenously inoculated into 20 NOG mice, all of which developed hind leg paralysis and distress around 6 weeks after transplantation. Pathological studies showed that only the bone marrow was infiltrated with U266 cells, and no cells were present in other organs. Osteolytic lesions in cortical bones and loss of trabecular bones were prominent in U266-transplanted NOG mice. In contrast, U266 cells were not detected in CB17scid or NOD/SCID mice 6 weeks after intravenous inoculation. Human IgE, produced by U266 cells, was detected in the serum of U266-transplanted NOG mice by ELISA. The results indicated that this hu-myeloma NOG model might be useful for studying the pathogenesis of myeloma and related osteolytic lesions, and are suggestive of its applicability to the future development of new drugs.
我们使用免疫缺陷的NOD/SCID/γc(null)(NOG)小鼠建立了一种新的人类多发性骨髓瘤实验动物模型。将人骨髓瘤细胞系U266静脉接种到20只NOG小鼠体内,所有小鼠在移植后约6周出现后腿麻痹和不适。病理研究表明,只有骨髓被U266细胞浸润,其他器官未发现细胞。在移植U266的NOG小鼠中,皮质骨的溶骨性病变和小梁骨的丢失很明显。相比之下,静脉接种6周后,在CB17scid或NOD/SCID小鼠中未检测到U266细胞。通过ELISA在移植U266的NOG小鼠血清中检测到U266细胞产生的人IgE。结果表明,这种人骨髓瘤NOG模型可能有助于研究骨髓瘤的发病机制和相关溶骨性病变,并提示其在新药未来开发中的适用性。