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戊糖途径对莫里斯肝癌5123C葡萄糖代谢的机制及定量贡献

Mechanism and quantitative contribution of the pentose pathway to the glucose metabolism of Morris hepatoma 5123C.

作者信息

Arora K K, Longenecker J P, Williams J F

出版信息

Int J Biochem. 1987;19(2):133-46. doi: 10.1016/0020-711x(87)90324-7.

Abstract

An investigation of the mechanism and quantitative contribution of the pentose phosphate pathway in the glucose metabolism of Morris Hepatoma 5123C is reported. Morris Hepatoma 5123C has an active non-oxidative segment of pentose pathway as judged by its ability to convert ribose 5-P to hexose 6-P in a standard assay. Based on compliance with qualitative and quantitative criteria, the cells exhibit the L-type pentose pathway reaction sequence rather than the F-type pathway. This compliance included the formation of intermediates characteristic of the L-type pathway, namely arabinose 5-P, octulose mono- and bisphosphates and sedoheptulose 1,7-bisphosphate, during the dissimilation of ribose 5-P to hexose 6-P. The intermediary role of arabinose 5-P was suggested by the incorporation of its carbon into various intermediates and products of the pentose pathway. Intermediary roles for ido octulose mono- and bisphosphates were supported by their participation in the reaction catalyzed by the phosphotransferase enzyme of the L-type pentose pathway. Presence of L-type PP reactions was further affirmed by 14C-prediction labelling experiments using [5-14C]- and [2-14C]glucose as specifically labelled substrates. Using two methods of measurement, the F-type pentose cycle made a negligibly small contribution to glucose metabolism, while the measured value of the L-type pentose pathway accounted for 30% (approx.) of the total glucose metabolism of these cells, a value consistent with the high activity of the enzymes of the L-type pentose pathway in Morris Hepatoma 5123C cells and the very high activity of the non-oxidative segment of the pathway in vitro. The findings validate the proposal that the L-type pentose pathway reactions constitute the non-oxidative segment of the pathway in Morris Hepatoma 5123C cells. Reasons involving pyruvate recycling reactions show why there is low incorporation of 14C-isotope in C-1 of glucose 6-P, when [4,5,6-14C]glucose and [6-14C]glucose are L-type PP test substrates in intact cells.

摘要

本文报道了对磷酸戊糖途径在莫里斯肝癌5123C葡萄糖代谢中的机制及定量贡献的研究。通过在标准测定中其将5-磷酸核糖转化为6-磷酸己糖的能力判断,莫里斯肝癌5123C具有活跃的磷酸戊糖途径非氧化段。基于符合定性和定量标准,这些细胞呈现L型磷酸戊糖途径反应序列而非F型途径。这种符合包括在5-磷酸核糖异化生成6-磷酸己糖过程中形成L型途径特有的中间产物,即5-磷酸阿拉伯糖、辛酮糖单磷酸和双磷酸以及景天庚酮糖1,7-双磷酸。5-磷酸阿拉伯糖的碳掺入磷酸戊糖途径的各种中间产物和产物中,提示了其作为中间产物的作用。艾杜辛酮糖单磷酸和双磷酸作为中间产物的作用得到其参与L型磷酸戊糖途径磷酸转移酶催化反应的支持。使用[5-¹⁴C]-和[2-¹⁴C]葡萄糖作为特异性标记底物的¹⁴C-预测标记实验进一步证实了L型磷酸戊糖反应的存在。使用两种测量方法,F型磷酸戊糖循环对葡萄糖代谢贡献极小,而L型磷酸戊糖途径的测量值占这些细胞总葡萄糖代谢的约30%,该值与莫里斯肝癌5123C细胞中L型磷酸戊糖途径酶的高活性以及该途径体外非氧化段的极高活性一致。这些发现验证了L型磷酸戊糖途径反应构成莫里斯肝癌5123C细胞中该途径非氧化段的提议。涉及丙酮酸循环反应的原因解释了为何当[4,5,6-¹⁴C]葡萄糖和[6-¹⁴C]葡萄糖作为完整细胞中L型磷酸戊糖测试底物时,6-磷酸葡萄糖C-1位的¹⁴C-同位素掺入率较低。

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