Bystryn J C
J Immunol. 1976 May;116(5):1302-5.
Synthesis and release of radiolabeled macromolecules and tumor-associated antigens (MAA) by murine B16 melanoma was studied by pulse labeling cells in culture with 3H-leucine. Approximately 36% of newly synthesized macromolecules and 44% of newly synthesized MAA were released in 48 hr. MAA release was slightly, but consistently, more rapid than the average release of other macromolecules. Release of MAA did not result solely from cell death since it was greater than that of 51Cr-labeled molecules and cell viability was over 98%. The rate of release of newly synthesized MAA was not significantly influenced by cell replication. However, synthesis of MAA was much greater during the logarithmic than the stationary phase of cell growth, suggesting a concomitant increase in the amount of MAA available for release. These findings indicate that antigens and other macromolecules can be rapidly released by viable tumor cells.
通过用³H-亮氨酸对培养中的细胞进行脉冲标记,研究了小鼠B16黑色素瘤对放射性标记大分子和肿瘤相关抗原(MAA)的合成与释放。在48小时内,约36%新合成的大分子和44%新合成的MAA被释放。MAA的释放略快于其他大分子的平均释放速度,且较为稳定。MAA的释放并非仅仅由细胞死亡导致,因为其释放量大于⁵¹Cr标记分子的释放量,且细胞活力超过98%。新合成MAA的释放速率不受细胞复制的显著影响。然而,在细胞生长的对数期,MAA的合成比稳定期要多得多,这表明可用于释放的MAA量随之增加。这些发现表明,活的肿瘤细胞能够快速释放抗原和其他大分子。