Plagemann P G
J Cell Biol. 1972 Jan;52(1):131-46. doi: 10.1083/jcb.52.1.131.
This study was undertaken to measure the absolute levels of nucleoside pools in Novikoff rat hepatoma cells (subline N1S1-67) during growth in suspension culture in the presence of high concentrations of various nucleosides in the medium, and to obtain further evidence for the compartmentalization of the nucleotides in independent cytoplasmic and nuclear pools. The levels of nucleotide pools were measured by growing the cells in medium supplemented with inorganic phosphate-(32)P. The nucleotide pool levels (mostly in the form of triphosphates) ranged from about 1 nmole of cytidine nucleotides to 8 nmole of adenosine nucleotides per 10(6) cells. The presence of 1 mM uridine, cytidine, guanosine, or adenosine in the medium resulted in marked increases in the intracellular levels of the corresponding nucleoside phosphates of at least 3-4 nmole/1O(6) cells. These increases were partially compensated for by decreases in the levels of other nucleotides. Evidence is presented to indicate that it is the cytoplasmic pool that expands during incubation with high concentrations of nucleosides in the medium, whereas the nuclear pool remains constant and very small in size. Preincubation of cells with 1 mM uridine-(3)H for 5.5 hr, which resulted in a threefold increase in the total intracellular level of uridine nucleotides, had no effect on the subsequent incorporation of uridine-(14)C into cellular nucleic acids in the nucleus, whether present at a 1 microM or 1 mM concentration in the medium. In contrast, the incorporation of uridine-(14)C into cytoplasmic viral-specific RNA by mengovirus-infected Novikoff cells was reduced 60-70% as a result of preincubation of the cells with high concentrations of uridine-(3)H. Further, within 1-2 min upon addition of 2.5 or 6.5 microM(3)H-labeled uridine, cytidine, adenosine, guanosine, or inosine to cultures of Novikoff rat hepatoma cells, the incorporation of label into nucleic acids reached a constant and maximum rate, in spite of the presence of high intracellular concentrations (0.4-3 mM) of the corresponding unlabeled nucleoside triphosphates. Marked differences were also observed in the relative incorporation of the various nucleosides into the different nucleotides of the acid-soluble pool, and of mengovirus RNA and cellular RNA.
本研究旨在测定诺维科夫大鼠肝癌细胞(亚系N1S1-67)在含有高浓度各种核苷的培养基中悬浮培养时核苷池的绝对水平,并获取进一步证据证明核苷酸在独立的细胞质和细胞核池中存在区室化。通过在补充有无机磷酸 - (32)P的培养基中培养细胞来测定核苷酸池的水平。核苷酸池水平(大多以三磷酸形式存在)范围为每10(6)个细胞中约1纳摩尔胞嘧啶核苷酸至8纳摩尔腺苷核苷酸。培养基中存在1 mM尿苷、胞苷、鸟苷或腺苷会导致相应核苷磷酸的细胞内水平显著增加,至少增加3 - 4纳摩尔/10(6)个细胞。这些增加部分被其他核苷酸水平的降低所补偿。有证据表明,在培养基中与高浓度核苷一起孵育期间,是细胞质池扩张,而细胞核池保持恒定且体积非常小。用1 mM尿苷 - (3)H预孵育细胞5.5小时,这导致尿苷核苷酸的细胞内总水平增加了三倍,但对随后尿苷 - (14)C掺入细胞核中的细胞核酸没有影响,无论其在培养基中的浓度是1 microM还是1 mM。相比之下,由于用高浓度尿苷 - (3)H预孵育细胞,诺维科夫细胞被脑心肌炎病毒感染后尿苷 - (14)C掺入细胞质病毒特异性RNA的量减少了60 - 70%。此外,在向诺维科夫大鼠肝癌细胞培养物中添加2.5或6.5 microM (3)H标记的尿苷、胞苷、腺苷、鸟苷或肌苷后的1 - 2分钟内,尽管存在高细胞内浓度(0.4 - 3 mM)的相应未标记核苷三磷酸,标记物掺入核酸的速率仍达到恒定且最大速率。在各种核苷相对掺入酸溶性池的不同核苷酸、脑心肌炎病毒RNA和细胞RNA方面也观察到了显著差异。