Gunning P W, Landreth G E, Layer P, Ignatius M, Shooter E M
J Neurosci. 1981 Apr;1(4):368-79. doi: 10.1523/JNEUROSCI.01-04-00368.1981.
The relationship between both DNA and RNA metabolism and the nerve growth factor (betaNGF)-induced differentiation of PC12 cells was investigated. Cells remained in log phase growth for 4 days after exposure to betaNGF. DNA synthesis was similarly unaffected by betaNGF during this time. Thereafter, a gradual decrease in DNA synthesis was observed. In contrast, as many as 40% of the cells display neurites after 4 days exposure to betaNGF. The implication, that cells which have begun to differentiate morphologically may still synthesize DNA, was confirmed using autoradiography. The cellular RNA concentration was elevated significantly within 1 day of exposure to betaNGF and continued to increase for up to 6 days. Dose-response analysis revealed that this increase in cellular RNA, both rRNA and tRNA, closely correlates with the size and number of neurites per cell rather than with the cell's capacity to grow a neurite per se. A parallel rise in the cellular protein concentration was observed also. It was concluded, therefore, that (1) cessation of cell division is not a prerequisite for the initiation of the morphological differentiation of these cells and (2) the elevation of the cellular RNA content influences some quantitative aspects of neurite outgrowth.
研究了DNA和RNA代谢与神经生长因子(βNGF)诱导的PC12细胞分化之间的关系。细胞在暴露于βNGF后保持对数期生长4天。在此期间,DNA合成同样不受βNGF影响。此后,观察到DNA合成逐渐减少。相比之下,在暴露于βNGF 4天后,多达40%的细胞长出神经突。使用放射自显影法证实了这样的推测,即已开始形态分化的细胞仍可能合成DNA。在暴露于βNGF的1天内,细胞RNA浓度显著升高,并持续增加长达6天。剂量反应分析表明,细胞RNA(包括rRNA和tRNA)的这种增加与每个细胞神经突的大小和数量密切相关,而不是与细胞本身长出神经突的能力相关。还观察到细胞蛋白质浓度平行升高。因此得出结论:(1)细胞分裂的停止不是这些细胞形态分化开始的先决条件;(2)细胞RNA含量的升高影响神经突生长的一些定量方面。