Bedi K S, Goldstein D J
J Cell Biol. 1976 Oct;71(1):68-88. doi: 10.1083/jcb.71.1.68.
The Feulgen-DNA contents of human leukocytes, sperm, and oral squames were investigated by scanning and integrating microdensitometry, both with and without correction for residual distribution error and glare. Maximally stained sperm had absorbances which at lambdamax exceeded the measuring range of the Vickers M86 microdensitometer; this potential source of error could be avoided either by using shorter hydrolysis times or by measuring at an off-peak wavelength. Small but statistically significant apparent differences between leukocyte types were found in uncorrected but not fully corrected measurements, and some apparent differences disappeared when only one of the residual instrumental errors was eliminated. In uncorrected measurements, the apparent Feulgen-DNA content of maximally stained polymorphs measured at lambdamax was significantly lower than that of squames, while in all experimental series uncorrected measurements showed apparent diploid:haploid ratios significantly greater than two. In fully corrected measurements no significant differences were found between leukocytes and squames, and in four independent estimations the lowest diploid:haploid ratio found was 1.99 +/- 0.05, and the highest 2.03 +/- 0.05. Discrepancies found in uncorrected measurements could be correlated with morphology of the nuclei concerned. Glare particularly affected measurements of relatively compact nuclei such as those of sperm, polymorphs and lymphocytes, while residual distribution error was especially marked with nuclei having a high perimeter:area ratio (e.g. sperm and polymorphs). Uncorrected instrumental errors, especially residual distribution error and glare, probably account for at least some of the previously reported apparent differences between the Feulgen-DNA contents of different cell types. On the basis of our experimental evidence, and a consideration of the published work of others, it appears that within the rather narrow limits of random experimental error there seems little or no reason to postulate either genuine differences in the amounts of DNA present in the cells studied, or nonstoichiometry of a correctly performed Feulgen reaction.
采用扫描和积分显微密度测定法对人白细胞、精子和口腔鳞状上皮细胞的福尔根 DNA 含量进行了研究,测量过程中分别校正和未校正残余分布误差及眩光。染色最深的精子在最大吸收波长处的吸光度超出了维氏 M86 显微密度计的测量范围;可以通过缩短水解时间或在非峰值波长处测量来避免这一潜在误差来源。在未校正但未完全校正的测量中,发现白细胞类型之间存在微小但具有统计学意义的表观差异,当仅消除其中一种残余仪器误差时,一些表观差异消失了。在未校正的测量中,在最大吸收波长处测量的染色最深的多形核白细胞的表观福尔根 DNA 含量显著低于鳞状上皮细胞,而在所有实验系列中,未校正的测量显示表观二倍体:单倍体比率显著大于 2。在完全校正的测量中,白细胞和鳞状上皮细胞之间未发现显著差异,在四次独立估计中,发现的最低二倍体:单倍体比率为 1.99±0.05,最高为 2.03±0.05。未校正测量中发现的差异可能与相关细胞核的形态有关。眩光尤其影响对相对致密细胞核(如精子、多形核白细胞和淋巴细胞的细胞核)的测量,而残余分布误差在周长:面积比高的细胞核(如精子和多形核白细胞)中尤为明显。未校正的仪器误差,尤其是残余分布误差和眩光,可能至少部分解释了先前报道的不同细胞类型福尔根 DNA 含量之间的表观差异。根据我们的实验证据,并考虑到其他人发表的研究成果,似乎在相当狭窄的随机实验误差范围内,几乎没有理由假定所研究细胞中存在的 DNA 量存在真正差异,或者正确进行的福尔根反应存在非化学计量关系。