Harris G
Immunology. 1973 Feb;24(2):343-63.
Explants of the spleens of rabbits previously primed to SRC and killed without boosting, were cultured with this antigen and the development of specific PFC (antibody-producing cells) was studied. The majority of PFC occurred in those cells which migrated from the explants into the medium and the antibodies produced by them did not require enhancement of their capacity to fix complement by developing antisera. The need for the continuous presence of antigen in the medium for optimal development of PFC was demonstrated. The majority of PFC arose from a DNA-synthesizing population of cells in these cultures, the migrating cells being very active in this respect. Only a small proportion of these DNA-synthesizing cells were found to be PFC, and it was also concluded that many cells were taking up radioactive material derived from other cells as well as labelled thymidine from the medium. Using colcemid to arrest cells in metaphase, no inhibition of the acute increase of PFC occurred during a 6-hour period of exposure indicating that this increase of these cells was not dependent on cell division. However this same increase of PFC was found to be highly radio-sensitive, indicating the involvement of DNA-dependent processes. It was therefore concluded that many cells including PFC, in these cultures were engaging in DNA synthesis without subsequent division. This was further emphasized by the observed rate of increase of PFC which was too rapid for the estimated rates of cell division, and the excessive number of cells labelling with [H]thymidine in relation to the mitotic rate.
将先前用SRC致敏并在未加强免疫的情况下处死的兔脾脏外植体与该抗原一起培养,并研究特异性PFC(抗体产生细胞)的发育情况。大多数PFC出现在从外植体迁移到培养基中的细胞中,并且它们产生的抗体不需要通过产生抗血清来增强其补体固定能力。证明了培养基中抗原的持续存在对于PFC的最佳发育是必需的。在这些培养物中,大多数PFC来自DNA合成细胞群体,迁移细胞在这方面非常活跃。发现这些DNA合成细胞中只有一小部分是PFC,并且还得出结论,许多细胞除了从培养基中摄取标记的胸苷外,还摄取来自其他细胞的放射性物质。使用秋水仙酰胺使细胞停滞在中期,在6小时的暴露期间未发生对PFC急性增加的抑制,表明这些细胞的增加不依赖于细胞分裂。然而,发现PFC的这种相同增加对放射高度敏感,表明涉及DNA依赖性过程。因此得出结论,这些培养物中的许多细胞包括PFC正在进行DNA合成而不随后分裂。这通过观察到的PFC增加速率进一步得到强调,该速率对于估计的细胞分裂速率来说太快,并且与有丝分裂速率相关的用[H]胸苷标记的细胞数量过多。