Daley M J, Williams T J, Giorgi J, Warner N L
Department of Pathology, University of New Mexico School of Medicine, Albuquerque 87131.
Cell Immunol. 1990 Apr 15;127(1):56-66. doi: 10.1016/0008-8749(90)90114-7.
A spontaneously arising murine plasmacytoma, HPC-202, derived from a BALB/c.H-2b congenic mouse that lacks any detectable H-2 determinants on its cell surface is described. However, the expression of H-2 determinants is inducible by interferon-gamma. The H-2 negative cell surface phenotype permits the HPC-202 tumor to escape H-2 allospecific cytotoxic cell lysis but not NK cell lysis, as well as to grow, to varying degrees, in some H-2 incompatible hosts. In those strains which exhibit a resistance to HPC-202 growth, resistance does not map to a single gene within the major histocompatibility complex of the mouse. Resistance is also radiosensitive and is therefore presumably due to a rapidly dividing cell population. The utility of this tumor as a model system to study both the non-H-2-restricted natural resistance to tumor growth, and the mechanism by which H-2 genes are regulated by cells is discussed.
描述了一种自发产生的小鼠浆细胞瘤HPC-202,它源自一只BALB/c.H-2b同源小鼠,其细胞表面缺乏任何可检测到的H-2决定簇。然而,H-2决定簇的表达可被γ干扰素诱导。H-2阴性细胞表面表型使HPC-202肿瘤能够逃避H-2同种异体特异性细胞毒性细胞的裂解,但不能逃避自然杀伤细胞的裂解,并且还能在一些H-2不相容的宿主中不同程度地生长。在那些对HPC-202生长表现出抗性的品系中,抗性并不定位于小鼠主要组织相容性复合体中的单个基因。抗性对辐射也敏感,因此推测是由于快速分裂的细胞群体所致。讨论了这种肿瘤作为模型系统在研究对肿瘤生长的非H-2限制的天然抗性以及H-2基因被细胞调节的机制方面的用途。