LOWE C U, RAND R N
J Biophys Biochem Cytol. 1956 Nov 25;2(6):711-24. doi: 10.1083/jcb.2.6.711.
Rats were treated with cortisone, x-radiation, and both agents in combination, and the effect noted on the DNA content of hepatocytes. Nuclei were enumerated both in whole liver homogenates and following isolation. The incorporation of P(32) into DNA was also studied in relation to these agents. The following observations were made:- 1.The DNA content of nuclei fell both during cortisone administration and following x-radiation. In the former instance, the fall was progressive with continuing administration of hormone; in the latter instance, there was a return to normal 5 days after radiation. 2. Cortisone administration to x-radiated rats caused a fall in DNA/nucleus and prevented the return to normal at 5 days. 3. There was no evidence that the effects of cortisone and x-rays were additive in reducing DNA/nucleus. 4. These data indicate an alteration in DNA/nucleus, but simple changes in ploidy cannot be excluded. Either explanation requires that the agents used affect the DNA of non-regenerating nuclei. 5. Cortisone interfered with the incorporation of P(32) into the DNA of regenerating liver. Only a small effect on DNA synthesis in resting liver was observed with cortisone or x-radiation. 6. DNA content of nuclei returned to normal 5 days after x-radiation and 3 days after discontinuance of cortisone. Slight increase in the incorporation of P(32) by DNA was observed during recovery phases. 7. The hypothesis is proposed that the apparent losses and increases in DNA/nucleus were due to depolymerization and repolymerization of DNA. Following x-radiation and/or cortisone administration, it is proposed that some DNA is depolymerized and becomes cold acid-soluble and dissociated from organized chromatin. Later, conditions are such that this degraded DNA is repolymerized. 8. These data might be interpreted to indicate that a portion of the DNA is not essential to cell integrity; alternatively, there may be two or more species of DNA, one of which is more readily affected by the agents investigated in the present report.
对大鼠分别给予可的松、X射线照射以及两者联合处理,并观察其对肝细胞DNA含量的影响。在全肝匀浆以及细胞核分离后均对细胞核进行计数。还研究了这些处理因素与P(32)掺入DNA的关系。得到以下观察结果:- 1. 在给予可的松期间以及X射线照射后,细胞核的DNA含量均下降。在前一种情况下,随着激素的持续给予,DNA含量逐渐下降;在后一种情况下,照射后5天DNA含量恢复正常。2. 对经X射线照射的大鼠给予可的松会导致细胞核DNA含量下降,并阻止其在5天时恢复正常。3. 没有证据表明可的松和X射线在降低细胞核DNA含量方面的作用是相加的。4. 这些数据表明细胞核DNA含量发生了改变,但不能排除倍性的简单变化。两种解释都需要所使用的处理因素影响非再生细胞核的DNA。5. 可的松干扰P(32)掺入再生肝的DNA。观察到可的松或X射线照射对静止肝DNA合成的影响很小。6. X射线照射后5天以及停止给予可的松3天后,细胞核DNA含量恢复正常。在恢复阶段观察到DNA对P(32)的掺入略有增加。7. 提出假说:细胞核DNA含量的明显减少和增加是由于DNA的解聚和再聚合。在给予X射线照射和/或可的松后,推测一些DNA发生解聚,变成冷酸溶性并从有组织的染色质中解离出来。之后,在某些条件下,这种降解的DNA会再聚合。8. 这些数据可以解释为表明一部分DNA对细胞完整性并非必不可少;或者,可能存在两种或更多种DNA,其中一种更容易受到本报告中所研究处理因素的影响。