Metabolism of radiolabeled glucose by mouse oocytes and oocyte-cumulus cell complexes

被引:143
作者
Downs, SM [1 ]
Utecht, AM [1 ]
机构
[1] Marquette Univ, Dept Biol, Milwaukee, WI 53201 USA
关键词
D O I
10.1095/biolreprod60.6.1446
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
This study was carried out to examine the metabolism of [1-C-14]-, [6-C-14]-, and [5-H-3]glucose by oocyte-cumulus cell complexes (OCC) and denuded oocytes (DO) and to test the hypothesis that metabolism of glucose through the pentose phosphate pathway is associated with meiotic induction. OCC or DO were cultured in hanging drops suspended from the cap of a microfuge tube, with NaOH serving as a frap to collect released (H2O)-H-3 or (CO2)-C-14. Preliminary experiments established that this culture system supports both spontaneous and ligand-induced meiotic maturation. An initial time course experiment (1.5-6 h) showed that hypoxanthine-treated OCC from eCG-primed animals metabolized glucose principally via glycolysis, with an increase to 2.7-fold in response to FSH. Though more [1-C-14]glucose was oxidized than [6-C-14]glucose, its metabolism was about two orders of magnitude less than that of [5-H-3]glucose, Also, FSH significantly increased oxidation of [1-C-14]glucose but not [6-C-14]glucose, indicating a preferential activation of the pentose phosphate pathway. Pyrroline carboxylate, an activator of the pentose phosphate pathway, increased the activity of this pathway to over 2-fold but failed to affect glucose oxidation through the tricarboxylic acid cycle. Glycolytic metabolism was increased by 25%. The addition of pyruvate to pyruvate-free medium resulted in significant reduction in the metabolism of all three glucose analogues. In OCC retrieved from hCG-injected, primed mice and cultured under hormone-free conditions, metabolic responses were similar to those in FSH-treated complexes cultured in hypoxanthine, DO metabolized glucose, but at a much reduced rate when compared to OCC, Pyruvate reduced the consumption of all three glucose analogues by DO. Pyrroline carboxylate reduced [5-H-3]glucose metabolism by DO but had little effect on [1-C-14]- and [6-C-14]glucose oxidation. These data demonstrate metabolism of glucose by both DO and OCC, but reveal that cumulus cells are more active than the oocyte in this regard. In addition, induction of maturation by FSH, hCG, or pyrroline carboxylate was accompanied by a significant increase in the oxidation of [1-C-14]glucose but not [6-C-14]glucose by OCC, supporting a proposed role for the pentose phosphate pathway in meiotic induction.
引用
收藏
页码:1446 / 1452
页数:7
相关论文
共 53 条
[1]   METHYLENE BLUE-MEDIATED HEXOSE-MONOPHOSPHATE SHUNT STIMULATION IN HUMAN RED-BLOOD-CELLS INVITRO - INDEPENDENCE FROM INTRACELLULAR OXIDATIVE INJURY [J].
BAIRD, JK .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY, 1984, 16 (10) :1053-1058
[2]   EXPLANATION FOR BLOCKADE OF GLYCOLYSIS IN EARLY MOUSE EMBRYOS [J].
BARBEHENN, EK ;
WALES, RG ;
LOWRY, OH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (04) :1056-1060
[3]   PATTERN OF ENERGY METABOLISM IN MOUSE OOCYTE AND ZYGOTE [J].
BIGGERS, JD ;
WHITTING.DG ;
DONAHUE, RP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1967, 58 (02) :560-&
[4]   GONADOTROPINS STIMULATE LACTATE PRODUCTION BY RAT CUMULUS AND GRANULOSA-CELLS [J].
BILLIG, H ;
HEDIN, L ;
MAGNUSSON, C .
ACTA ENDOCRINOLOGICA, 1983, 103 (04) :562-566
[5]  
BRINSTER RL, 1971, J REPROD FERTIL, V24, P187
[6]  
BRINSTER RL, 1968, ENZYMOLOGIA, V34, P304
[7]  
BRINSTER RL, 1966, BIOCHEM J, V101, P166
[8]   INTER-CELLULAR COMMUNICATION BETWEEN GRANULOSA-CELLS AND MOUSE OOCYTES - EXISTENCE AND POSSIBLE NUTRITIONAL ROLE DURING OOCYTE GROWTH [J].
BROWER, PT ;
SCHULTZ, RM .
DEVELOPMENTAL BIOLOGY, 1982, 90 (01) :144-153
[9]   CONTRAST IN LEVELS OF METABOLIC ENZYMES IN HUMAN AND MOUSE OVA [J].
CHI, MMY ;
MANCHESTER, JK ;
YANG, VC ;
CURATO, AD ;
STRICKLER, RC ;
LOWRY, OH .
BIOLOGY OF REPRODUCTION, 1988, 39 (02) :295-307
[10]   RAT OOCYTE MATURATION INVITRO - RELIEF OF CYCLIC-AMP INHIBITION BY GONADOTROPINS [J].
DEKEL, N ;
BEERS, WH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (09) :4369-4373