返回搜索

Gluconeogenesis

Reactome ID: R-HSA-70263

中文名称

糖异生

通路描述

糖异生将线粒体丙酮酸转化为细胞质葡萄糖 6-磷酸,后者可水解为葡萄糖并排出细胞。糖异生局限于肝脏和肾脏细胞,并在没有外源葡萄糖时,从乳酸、丙氨酸和其他氨基酸等分子合成葡萄糖(综述,例如 Chourpiliadis 和 Mohiuddin 2022)。糖异生分为两部分:反应网络将线粒体丙酮酸转化为细胞质磷酸烯醇丙酮酸;然后磷酸烯醇丙酮酸在一系列细胞质反应中转化为葡萄糖 6-磷酸。该过程的第一个部分有三个生理上重要的变体。1)一系列转运和转氨基反应将线粒体草酰乙酸转化为细胞质草酰乙酸,后者由激素调节的细胞质磷酸烯醇丙酮羧激酶异构体转化为磷酸烯醇丙酮酸。此变体允许从乳酸调节葡萄糖合成。2)线粒体草酰乙酸被还原为马氨酸,然后转运到细胞质并氧化为草酰乙酸。此变体为细胞提供还原当量,用于从如丙氨酸和谷氨酰胺等氨基酸合成葡萄糖。3) Constitutively 表达的线粒体磷酸烯醇丙酮羧激酶催化线粒体草酰乙酸转化为磷酸烯醇丙酮酸,然后可转运到细胞质。任何分子通过此反应网络的路径取决于发生反应的细胞类型、丙酮酸的来源以及触发糖异生的生理压力。在糖异生的第二部分中,尽管磷酸烯醇丙酮酸源自细胞质,但它通过与糖酵解步骤相反的反应转化为果糖 1,6-二磷酸。果糖 1,6-二磷酸的水解由果糖 1,6-二磷酸酶催化,生成果糖 6-磷酸,后者可逆异构化为葡萄糖 6-磷酸。在所有情况下,从两分子丙酮酸合成葡萄糖需要生成和消耗两分子细胞质 NADH + H+。来自乳酸的丙酮酸(变体 1 和 3)在细胞质中通过乳酸氧化为丙酮酸生成 NADH + H+(这是丙酮酸代谢反应,未在图中显示)。来自氨基酸的丙酮酸(变体 2)由谷氨酸脱氢酶(氨基酸代谢反应,未在图中显示)生成的线粒体 NADH + H+ 用于将草酰乙酸还原为马氨酸,后者转运到细胞质并氧化,生成细胞质 NADH + H+。从丙酮酸合成葡萄糖还需要消耗六个高能磷酸键,其中四个来自 ATP,两个来自 GTP。
英文描述
Gluconeogenesis Gluconeogenesis converts mitochondrial pyruvate to cytosolic glucose 6 phosphate which in turn can be hydrolyzed to glucose and exported from the cell. Gluconeogenesis is confined to cells of the liver and kidney and enables glucose synthesis from molecules such as lactate and alanine and other amino acids when exogenous glucose is not available (reviewed, e.g., by Chourpiliadis & Mohiuddin 2022). Gluconeogenesis occurs in two parts: a network of reactions converts mitochondrial pyruvate to cytosolic phosphoenolpyruvate; then phosphoenolpyruvate is converted to glucose 6 phosphate in a single sequence of cytosolic reactions.Three variants of the first part of the process are physiologically important. 1) A series of transport and transamination reactions convert mitochondrial oxaloacetate to cytosolic oxaloacetate which is converted to phosphoenolpyruvate by a hormonally regulated, cytosolic isoform of phosphoenolpyruvate carboxykinase. This variant allows regulated glucose synthesis from lactate. 2) Mitochondrial oxaloacetate is reduced to malate, which is exported to the cytosol and re oxidized to oxaloacetate. This variant provides reducing equivalents to the cytosol, needed for glucose synthesis from amino acids such as alanine and glutamine. 3) Constitutively expressed mitochondrial phosphoenolpyruvate carboxykinase catalyzes the conversion of mitochondrial oxaloacetate to phosphoenolpyruvate which may then be transported to the cytosol. The exact path followed by any one molecule of pyruvate through this reaction network is determined by the tissue in which the reactions are occurring, the source of the pyruvate, and the physiological stress that triggered gluconeogenesis.In the second part of gluconeogenesis, cytosolic phosphoenolpyruvate, however derived, is converted to fructose 1,6 bisphosphate by reactions that are the reverse of steps of glycolysis. Hydrolysis of fructose 1,6 bisphosphate to fructose 6 phosphate is catalyzed by fructose 1,6 bisphosphatase, and fructose 6 phosphate is reversibly isomerized to glucose 6 phosphate.In all cases, the synthesis of glucose from two molecules of pyruvate requires the generation and consumption of two reducing equivalents as cytosolic NADH + H+. For pyruvate derived from lactate (variants 1 and 3), NADH + H+ is generated with the oxidation of lactate to pyruvate in the cytosol (a reaction of pyruvate metabolism not shown in the diagram). For pyruvate derived from amino acids (variant 2), mitochondrial NADH + H+ generated by glutamate dehydrogenase (a reaction of amino acid metabolism, not shown) is used to reduce oxaloacetate to malate, which is transported to the cytosol and re oxidized, generating cytosolic NADH + H+. The synthesis of glucose from pyruvate also requires the consumption of six high energy phosphates, four from ATP and two from GTP.

所含基因

25 个基因