Simonneau L, Crisanti P, Lorinet A M, Alliot F, Courtois Y, Calothy G, Pessac B
Mol Cell Biol. 1986 Nov;6(11):3704-10. doi: 10.1128/mcb.6.11.3704-3710.1986.
The lens-specific proteins alpha and delta crystallins and lentoid bodies, structures that follow a differentiation pathway similar to that of the lens, regularly appear after 4 to 5 weeks in quail embryo neuroretina monolayer cultures. We have investigated the effects of the avian oncogenic retroviruses Mill Hill 2 and Rous sarcoma virus on this process. Quail embryo neuroretina cells transformed by Mill Hill 2 virus were established into permanent cultures that synthesized alpha and delta crystallins and contained stem cells for the production of lentoid bodies. In contrast, transformation with the Rous sarcoma virus mutant tsNY-68 blocked the appearance of mRNA crystallins, but cytoplasmic alpha and delta crystallin mRNA and alpha crystallin appeared 44 h after a shift to the nonpermissive temperature. However, delta crystallins and lentoid bodies were only present after 7 days. The crystallins of transformed quail neuroretina cultures were immunologically indistinguishable from those of quail lenses and of normal quail embryo neuroretina cultures.
晶状体特异性蛋白α和δ晶状体蛋白以及类晶状体小体(其结构遵循与晶状体相似的分化途径)在鹌鹑胚胎神经视网膜单层培养物中4至5周后会定期出现。我们研究了禽致癌逆转录病毒米尔希尔2号病毒和劳斯肉瘤病毒对这一过程的影响。由米尔希尔2号病毒转化的鹌鹑胚胎神经视网膜细胞被建立成永久性培养物,这些培养物合成α和δ晶状体蛋白,并含有产生类晶状体小体的干细胞。相比之下,用劳斯肉瘤病毒突变体tsNY - 68进行转化会阻断晶状体蛋白mRNA的出现,但在转移到非允许温度44小时后,细胞质中的α和δ晶状体蛋白mRNA以及α晶状体蛋白出现了。然而,δ晶状体蛋白和类晶状体小体仅在7天后出现。转化后的鹌鹑神经视网膜培养物中的晶状体蛋白在免疫学上与鹌鹑晶状体和正常鹌鹑胚胎神经视网膜培养物中的晶状体蛋白无法区分。