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小鼠肝脏实质细胞和非实质细胞中糖酵解及糖异生酶的活性

Glycolytic and gluconeogenic enzyme activities in parenchymal and non-parenchymal cells from mouse liver.

作者信息

Crisp D M, Pogson C I

出版信息

Biochem J. 1972 Feb;126(4):1009-23. doi: 10.1042/bj1261009.

Abstract
  1. Parenchymal cells have been prepared from mouse liver by enzymic and mechanical means. 2. The dry weights, protein and DNA contents of these cells have been determined. 3. Mouse liver ;M-' and ;L-type' pyruvate kinases have been prepared free of contamination with each other; their kinetic properties have been examined and a method has been developed for their assay in total liver homogenates. 4. Recoveries of phosphoglycerate kinase, lactate dehydrogenase and phosphofructokinase in enzymically prepared cells indicate that little, if any, cytoplasmic protein is lost during preparation. 5. Parenchymal cells exhibit a very substantial increase in the activity ratio of glucokinase to hexokinase over that in total liver homogenate; in three out of eight experiments, hexokinase activity was undetectable. 6. ;L-type' pyruvate kinase alone occurs in the parenchymal cell. Non-parenchymal cells are characterized by the presence of ;M-type' activity only. 7. Parenchymal cells contain both glucose 6-phosphatase and fructose 1,6-diphosphatase. The non-parenchymal fraction appears to contain fructose 1,6-diphosphatase, but is devoid of glucose 6-phosphatase. 8. No aldolase A was detectable in the whole liver. Aldolase B occurs in both parenchymal and non-parenchymal tissue. 9. Parenchymal cells prepared by mechanical disruption of mouse liver with 20% polyvinyl alcohol exhibit a similar enzyme profile to those prepared enzymically. 10. The methodology involved in the preparation of isolated liver cells is discussed. The importance of the measurement of several parameters as criteria for establishing the viability of parenchymal cells is stressed. 11. The metabolic implications of the results in the present study are discussed.
摘要
  1. 已通过酶解和机械方法从小鼠肝脏中制备了实质细胞。2. 测定了这些细胞的干重、蛋白质和DNA含量。3. 已分别制备了不含相互污染的小鼠肝脏“M型”和“L型”丙酮酸激酶;检测了它们的动力学特性,并开发了一种在全肝匀浆中测定它们的方法。4. 酶解制备的细胞中磷酸甘油酸激酶、乳酸脱氢酶和磷酸果糖激酶的回收率表明,制备过程中即使有细胞质蛋白丢失,量也很少。5. 实质细胞中葡萄糖激酶与己糖激酶的活性比相对于全肝匀浆有非常显著的增加;在八项实验中的三项中,未检测到己糖激酶活性。6. 实质细胞中仅存在“L型”丙酮酸激酶。非实质细胞的特征仅在于存在“M型”活性。7. 实质细胞同时含有葡萄糖6-磷酸酶和果糖1,6-二磷酸酶。非实质部分似乎含有果糖1,6-二磷酸酶,但不含葡萄糖6-磷酸酶。8. 在整个肝脏中未检测到醛缩酶A。醛缩酶B存在于实质和非实质组织中。9. 用20%聚乙烯醇机械破碎小鼠肝脏制备的实质细胞与酶解制备的细胞具有相似的酶谱。10. 讨论了分离肝细胞制备过程中涉及的方法。强调了测量几个参数作为确定实质细胞活力标准的重要性。11. 讨论了本研究结果的代谢意义。

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