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不同倍性大鼠肝实质细胞酸性磷酸酶的定量细胞化学研究。

A quantitative cytochemical study of acid phosphatases in rat liver parenchymal cells of different ploidy values.

作者信息

Middleton J, Gahan P B

出版信息

Histochem J. 1979 Nov;11(6):649-59. doi: 10.1007/BF01004729.

Abstract

The Vickers M86 integrating microdensitometer has been used to quantify the cytochemical reaction for acid naphthol AS-BI phosphatase activity in isolated, rat liver parenchymal cells. Data are presented which validate the method. The use of this method together with that of the Feulgen reaction to estimate nuclear ploidy value in the same cell, has shown that there is an increase in acid phosphatase activity of up to 100% when the euploidy value of the liver cell doubles. It has been further shown that 70--80% of this enzyme activity is ouabain-sensitive, regardless of the euploidy value. The data may be interpreted to indicate that the extra gene copies of the polyploid cells are operative.

摘要

维氏M86积分显微密度计已被用于定量测定分离的大鼠肝实质细胞中酸性萘酚AS-BI磷酸酶活性的细胞化学反应。文中给出的数据验证了该方法。将此方法与福尔根反应结合使用,以估计同一细胞中的核倍性值,结果表明,当肝细胞的整倍性值加倍时,酸性磷酸酶活性增加高达100%。进一步表明,无论整倍性值如何,该酶活性的70%-80%对哇巴因敏感。这些数据可以解释为表明多倍体细胞的额外基因拷贝是有活性的。

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