丙酮酸调控小鼠卵母细胞排卵后老化的研究
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摘要
卵母细胞排卵后老化显著影响其胚胎发育。排卵后老化的卵母细胞受精后出生的小鼠表现出神经敏感和情绪的异常。与输卵管内滞留一样,体外培养成熟卵母细胞也会导致卵母细胞老化。然而,人类和一些动物通常可以在发情周期的任何一天从事性行为,这可能导致排卵后老化的卵母细胞受精。另外,许多研究和临床应用的实验设计都涉及成熟卵母细胞在显微操作和授精前的体外培养。因此,研究卵母细胞老化的机制并且调控卵母细胞老化无论对人类还是非人类动物的健康生殖都是非常重要的。
     老化卵母细胞最明显的特征包括对激活刺激敏感性的增加、MPF活性降低、后期II的启动、皮质颗粒部分胞吐、线粒体聚集、微管组装变化,并出现细胞凋亡的征兆,例如胞质和DNA断裂以及Bcl-2蛋白水平的降低。另外,老化的小鼠卵母细胞中组蛋白的某些赖氨酸位点乙酰化水平增加,而且由于老化过程中的氧化应激造成ROS的累积,并改变卵母细胞内的氧化还原状态,造成卵母细胞内总的GSH量减少以及GSH/GSSG比例的降低。
     我们之前的研究证明卵丘细胞能够促进小鼠卵母细胞老化。然而,卵丘细胞促进卵母细胞老化的确切机制还不清楚。据报道成熟卵母细胞能够代谢丙酮酸,并且在不含葡萄糖的培养基中卵丘卵母细胞复合体(COCs)比裸卵(DOs)消耗更多的丙酮酸。我们猜测卵母细胞在不含丙酮酸的条件下老化的更快,并且卵丘细胞可能通过消耗不含葡萄糖的CZB中的丙酮酸从而促进卵母细胞老化。为了验证这个猜测,我们将新排卵的小鼠卵母细胞培养在添加不同浓度丙酮酸的CZB中,然后进行激活处理或通过放射自显影的方法分析MPF活性。结果发现丙酮酸以剂量依赖性的方式降低COCs和DOs的激活率,而升高其MPF活性,卵丘细胞存在的情况下需要更多的丙酮酸。新鲜排卵的DOs培养在不另外添加丙酮酸的COCs条件化的CZB中,其激活率显著升高,MPF活性显著降低,然而,当在条件化培养基中添加10 mM丙酮酸后,DOs的激活率和MPF活性都与新鲜卵母细胞无差别。我们通过毛细管电泳试验证明,COCs和卵丘细胞单层制备的CZB条件化培养基中丙酮酸的含量显著低于新鲜制备的CZB、单独培养的CZB以及DOs条件化的CZB中丙酮酸的含量。这些结果有力地验证了我们的猜测:在不含葡萄糖的培养液中卵丘细胞通过消耗丙酮酸从而促进卵母细胞老化。
     为了检测丙酮酸对卵母细胞其他老化指标的影响,我们通过免疫荧光显微镜检查法观察了皮质颗粒的提前胞吐、线粒体分布、微管组装、抗凋亡蛋白Bcl-2水平、组蛋白乙酰化水平,通过Hoechst33342染色观察了后期II的启动,通过体外受精及其随后的胚胎发育能力检测了丙酮酸对老化卵母细胞发育潜力的影响。结果证明,丙酮酸能够显著抑制老化卵母细胞皮质颗粒的提前胞吐、线粒体聚集、微管组装的变化;并且显著抑制了Bcl-2、组蛋白乙酰化水平以及胞质碎裂比例的升高,说明丙酮酸能够显著抑制老化小鼠卵母细胞的凋亡。另外,我们的数据还证明老化过程中添加丙酮酸能够显著抑制老化对卵母细胞受精及其发育能力所造成的损伤。这些数据表明,丙酮酸能够显著抑制COCs和DOs的老化。
     为了验证丙酮酸是否通过其抗氧化作用从而抑制卵母细胞老化,我们通过2’,7’-dichlorodihydrofluorescein diacetate (DCHFDA)染色的方法检测了老化卵母细胞内ROS的水平,并通过DTNB-GSSG还原酶实验检测了老化卵母细胞内总GSH、还原型GSH水平以及GSH/GSSG比例。结果表明,丙酮酸能够显著抑制老化卵母细胞中ROS水平的增加,并且能够显著抑制总GSH和GSH水平以及GSH/GSSG比例的降低。这些数据表明,丙酮酸可能通过其抗氧化作用维持细胞内的氧化还原水平,显著削弱卵母细胞老化过程中的氧化应激对其造成的损伤。
     因此,我们得出结论:丙酮酸能够抑制小鼠COCs和DOs的老化,卵丘细胞通过消耗培养液中的丙酮酸从而促进卵母细胞老化。而且,从我们现在的数据可以看出,很显然在卵母细胞老化过程中添加丙酮酸能够显著提高排卵后老化卵母细胞的质量,并降低其凋亡指标。丙酮酸很可能通过其抗氧化作用从而维持卵母细胞GSH/GSSG比例,并阻止总GSH含量的降低以及胞质内ROS水平的升高,从而显著抑制凋亡的发生。
Postovulatory aging of oocytes significantly affects embryonic development. Fertilization of postovulatory aged oocytes gives rise to mice suffering from nervous and emotional abnormalities and decreased reproductive fitness and longevity Like detention in the oviduct, in vitro culture of matured oocytes also led to oocyte aging. However, human beings and some animals potentially undertake sexual activity on any day of the estrous cycle, which may cause fertilization of aged ovulated oocytes. In addition, many experimental designs in both research and clinical applications involve culture of matured oocytes prior to micromanipulation or insemination. Therefore, studies on the mechanisms and control of oocyte aging are important for the healthy reproduction of both human beings and nonhuman mammals.
     The most prominent manifestations of aged oocytes include an increased susceptibility to activating stimuli, a decrease in MPF activity, the onset of anaphase II, a partial exocytosis of cortical granules, mitochondria aggregation, changes in microtubule assembly and signs of apoptotic cell death such as increased cytoplasmic and DNA fragmentation and decreased levels of Bcl-2 proteins. In addition, an increased acetylation on some lysines of histones and intracellular levels of ROS was increased for the reason of oxidative stress during aging process, subsequently decreased the level of total GSH and the ratio of GSH/GSSG. Our previous studies showed that cumulus cells accelerated aging of mouse oocytes.
     However, the exact mechanism by which cumulus cells promote oocyte aging is unknown. Since it was reported that matured oocytes were capable of metabolizing pyruvate and that cumulus-oocyte complexes (COCs) consumed much more pyruvate than cumulus-denuded oocytes (DOs) in the absence of glucose, we hypothesized that oocytes would age quickly in the absence of pyruvate, and cumulus cells would accelerate oocyte aging by depleting pyruvate in the CZB medium that contains no glucose. The objective of this study was to test this hypothesis. Newly ovulated mouse oocytes were cultured in the CZB medium supplemented with different concentrations of pyruvate before treated for activation or assayed for MPF activity. While pyruvate decreased the susceptibility to activation stimulus while increased the MPF activity of both COCs and DOs in a dose-dependent manner, more pyruvate was needed in the presence than in absence of cumulus cells. When newly ovulated DOs were cultured in COCs-conditioned CZB without pyruvate supplementation, activation rates increased while MPF activity decreased significantly; however, when cultured in conditioned CZB supplemented with 10 mM pyruvate, both activation rates and MPF activity remained close to those of newly ovulated control oocytes. Capillary electrophoresis showed that CZB conditioned with COCs or cumulus cells contained significantly less pyruvate than freshly prepared CZB and CZB conditioned with DOs or without cells. These results have fully born out our hypothesis that cumulus cells accelerate oocyte aging by depleting pyruvate in the culture medium that contains no glucose.
     In order to detect the effects of pyruvate on the other indicators of oocytes aging, we observed the premature exocytosis of cortical granules, mitochondria distribution, microtuble assembly, levels of Bcl-2 and histone acetylation through immunofluorescence microscopy; Observed the onset of anaphase II by Hoechst 33342 staining. We also detected the effects of pyruvate on the development potential of aging oocytes through in vitro fertilizaion and subsequent embryonic development. This results suggested that pyrvate can significantly inhibit premature exocytosis of cortical granules, mitochondria aggregation and changes in microtuble assembly; and significantly prevented the decreases of levels of Bcl-2, histone acetylation and the rates of cytoplasmic fragmentation, indicated that pyruvate prevented apoptosis of aging mouse oocytes. In addation, the present results also suggested that pyruvate can significantly weaken the detrimental effects of postovulatory aging on the developmental potential of oocytes. This data confirmed that pyruvate inhibited aging of both COCs and DOs.
     In order to verify whether the pyruvate inhibited the aging of oocytes through its antioxidative ability we evaluated the intracellular level of ROS through 2 ', 7'-dichlorodihydrofluorescein diacetate (DCHFDA) staining method; and assaied the levels of total GSH, reduced GSH and the ratio of GSH/GSSG through DTNB-GSSG Reductase experiment. The results showed that pyruvate could significantly prevent the increase in the level of ROS, and the decrease of levels of total GSH and reduced GSH and the ratio of GSH/GSSG. It is concluded that pyruvate could maintain the redox state of the aging oocytes and significantly weaken the injury of oocytes resulted from oxidative stress during postovulatory aging.
     Therefore, we conclude that pyruvate could inhibit the aging of both COCs and DOs, cumulus cells accelerate oocyte aging by depleting pyruvate in the culture medium that contains no glucose. And from the data presented, it is apparent that the supplementation of pyruvate during oocytes aging had several beneficial effects on the qualities of postovulated oocytes and reduced multiple measures of apoptosis. One beneficial effect of pyruvate in preventing the apoptosis is the favorable maintenance of the oocytes GSH-to GSSG ratio and prevention of a decrease in total glutathione content and the increase in ROS maybe through its antioxidative activites.
引文
孙青原,秦鹏春,刘国艺,杨庆章.牛卵丘-卵母细胞复合体体外成熟前后的超微结构. 东北农业大学学报. 1996; 27: 158-164.
    谭景和.脊椎动物比较胚胎学.黑龙江教育出版社. 1996.第一版
    翟中和,王喜忠,丁孝明.细胞生物学.高等教育出版社. 2000.第一版
    沈同,王镜岩,赵邦悌,李建武,徐长法,朱圣庚,俞梅敏,杨端,杨福愉.生物化学.高等教育出版社. 2002.第一版(重印)
    Abbott AL, Xu Z, Kopf GS, Ducibella T, Schultz RM. In vitro culture retards spontaneous activation of cell cycle progression and cortical granule exocytosis that normally occur in in vivo unfertilized mouse eggs. Bio Reprod 1998; 59: 1515-1512.
    Abeydeera LR, Wang W-H, Cantley TC, Rieke A, Day BN. Co-culture with follicular shell pieces can enhance the developmental competence of pig oocytes after in vitro fertilization: Relevance to intracellular glutathione. Bio Reprod 1998, 58: 213-218.
    Akiyama T, Nagata M, Aoki F. Inadequate histone deacetylation during oocyte meiosis causes aneuploidy and embyuo death in mice. PNAS 2006; 103:7339-7344.
    Armstrong JS, Steinauer KK, Hornung B, et al. Role of glutathione depletion and reactive oxygen species generation in apoptotic signaling in a human B lymphoma cell line. Cell Death Differ. 2002; 9 (3) : 252-263.
    Azam S., Hadi N., Khan N U, and Hadi, S. M. Antioxidant and prooxidant properties of caffeine, theobromine and xanthine, Med. Sci. Monit 2003, 9: BR325-330.
    Bakowski D, Parekh AB. Regulation of store-operated calcium channels by the intermediary metabolite pyruvic acid. Curr Biol 2007; 17: 1076-1081.
    Bernard O, Balasubramanian KA. Effect of oxidized glutathione on intestinal mitochondria and brush border membrane. International Journal of Biochemistry and Cell Biology 1995; 27: 589-595.
    Berridge MJ, Bootman MD and Lipp P. Calcium– a life and death signal. Nature 1998; 395: 645-648.
    Berridge MJ, Bootman MD, Roderick HL. Calcium sihnalling: Dynamics, homeostasis and renodelling. Mol Cell Biol 2003; 4: 517-529.
    Bian X, Hughes FM, Jr, Huang Y, Cidlowski JA and Putney JW, Jr. Roles of cytoplasmic Ca2+ and intracellular Ca2+ stores in induction and suppression of apoptosis in S49 cells. American Journal of Physiology 1997; 272: C1241-C1249.
    Biggers JD, Whittingham DG, Donahue RP. The pattern of energy metabolism in the mouse oocyte and zygote. PNAS 1967; 58: 560-567.
    Boerjan, M.L. and de Boer, P. First cell cycle of zygotes of the mouse derived from oocytes aged postovulation in vivo and fertilized in vivo. Mol Reprod Dev 1990; 25: 155-163.
    Borle AB and Stanko RT. Pyruvate reduces anoxic injury and free radical formation in perfused rat hepatocytes. Am J Physiol Gastrointest Liver Physiol 1996; 270: G535-G540.
    Boulares AH, Zoltoski AJ, Contreras FJ, Yakovlev AG, Yoshihara K, and Smulson ME. Regulation of DNAS1L3 endonuclease activity by poly (ADP-ribosyl) ation during etoposideinduced apoptosis. Role of poly (ADP-ribose) polymerase-1 cleavage in endonuclease activation. J Biol Chem 2002; 277: 372-378.
    Brad AM, Bormann CL, Swain JE, Durkin RE, Johnson AE, Clifford AL. Glutathione and adenosine triphosphate content of in vivo and in vitro matured porcine oocytes. Mol Reprod Dev 2003; 64: 492-498.
    Calvin HI, Grosshans K, Blake EJ. Estimation of glutathione concentrations in prepubertal mouse ovaries and ova: Relevance to sperm nucleus transformation in the fertilized egg. Gamete Res 1986; 14: 265-275.
    Carafoli E. Calcium signaling: A tale for all seasons. PNAS 2002, 99: 1115-1122.
    Chang DC,Meng C. A localized elevation of cytosolic free calcium is associated with cytokinesis in the zebrafish embryo. J Cell Biol 1995; 131(6 Pt 1): 1539-1545
    Chen Q, Chai YC, Mazumder S, et al. The late increase in intracellular free radical oxygen species during apoptosis is associated with cytochrome c release, caspase activation, and mitochondrial dysfunction. Cell Death Differ 2003; 10 (3) :323-334.
    Chi MM, Manchester JK, Yang VC, Curato AD, Strickler RC and Lowry OH. Contrast in the levels of metabolic enzymes in human and mouse ova Biology of Reproduction 1988; 39: 295-307.
    Choi TS, Mori M, Kohmoto K, Shoda U. Beneficial eddect of serum on the fertilizability ofmouse oocytes matured in vitro. J Reprod Fertil 1987; 79: 565-568.
    Chung SJ, Lee SH, Lee YJ, Park HS, Bunger R, Kang YH. Pyruvate protection against endothelial cytotoxicity induced by blockade of glucose uptake. J Biochem Mol Biol 2004; 37: 239-245.
    Clague JR, Langer GA. The pathogenesis of flee radical-induced calcium leak in cultured rat cardiomyocytes. J Mol Cell Cordiol 1994; 26(1): l1-21.
    Clem RJ, Cheng EH, Karp CL, Kirsch DG, Ueno K, Takahashi A, Kastan MB, Griffin DE, Earnshaw WC, Veliuona MA, and Hardwick JM. Modulation of cell death by Bcl-XL through caspase interaction. Proc Natl Acad Sci USA 1998; 95: 554-559.
    Coffey RN, Watson RW, Hegarty PK, et al. Priming prostate carcinoma cells for increased apoptosis is associated with up-regulation of the caspases. Cancer 2001; 92 (9) : 2297-2308.
    Cohen J, Scott R, Alikani M, Schimmel T, Munne S, Levron J, Wu L, Brenner C, Warner C and Willadsen S. Ooplasmic transfer in mature human oocytes Molecular Human Reproduction 1998; 4: 269-280.
    Colledge WH, Carlton MBL, Udy GB, Evans MJ. Disruption of c-mos causes parthenogenetic development of unfertilized mouse eggs. Nature 1994; 370:65-68.
    Csordás G, Thomas AP and Hajnóczky G. Quasi-synaptic calcium signal transmission between endoplasmic reticulum and mitochondria. EMBO Journal 1999; 18: 96-108.
    Cuthbertson KS,CobboldPH. Phorbol ester and sperm activate mouse oocyte by inducing sustained oscillations in cell Ca2+ Nature 1985; 316:541-542.
    de Lamirande E, Gagnon C. Reactive oxygen species and human spermatozoa. II. Depletion of adenosine triphosphate plays an important role in the inhibition of sperm motility. J Androl 1992; 13: 379-386.
    De Matos DG, Furnus CC, Moses DF. Glutathione synthesis during in vitro maturation of bovine oocytes: Role of cumulus cells. Biol Reprod 1997; 57: 1420-1425.
    De Matos DG, Furnus CC. The importance of having high glutathione (GSH) level after bovine in vitro maturation on embryo development: Effect ofβ- mercaptoethanol, cystein and cystin. Theriogenology 2000; 53: 761-771.
    Diestelhorst CW and Dubyak G. Role of calcium in glucocorticosteroid-induced apoptosis ofthymocytes and lymphoma cells: resurrection of old theories by new findings. Blood 1998; 91: 731-734.
    Ding WX, Shen HM, Ong CN. Critical role of reactive oxygen species and mitochondrial permeability transition in microcysth-induced rapid apoptosis in rat hepatocytes. Hepatology 2000; 32 (3) : 547-555.
    Domenicotti C, Paola D, Vitali A, Nitti M, d’Abramo C, Cottalasso D, Maloberti G, Biasi F, Poli G, Chiarpotto E, Marinari UM, and Pronzato MA. Glutathione depletion induces apoptosis of rat hepatocytes through activation of protein kinase C novel isoforms and dependent increase in AP-1 nuclear binding. Free Radic Biol Med 2000; 29: 1280-1290.
    Downs SM, Humpherson PG, Leese HJ. Pyruvate utilization by mouse oocytes is influenced by meiotic status and the cumulus oophorus. Mol Reprod Dev 2000; 62:113-123.
    Ducibella T, Duffy P, Reindollar R, Su B. Change in the distribution of mouse oocyte cortical granules and ability to undergo the cortical reaction during gonadotropin-stimulated meiotic maturation and aging in vivo. Biol Reprod 1990; 43: 870-876.
    Ducibella T, Huneau D, Angelichio E, Xu Z, Schultz RM, Kopf GS, Fissor R, Madoux S, Ozil JP. Egg-to-embryo transition is driven by different response to Ca2+ oscillation number. Dev Biol 2002; 250:280-291.
    Endo T, Naito K, Aoki F, Kume S, Tojo H. Changes in histone modifications during in vitro maturation of porcine oocytes. Mol Reprod Dev 2005, 71:123-128.
    Eppig JJ, Wigglesworth K, O’Brien MJ. Comparison of embryonic developmental competence of mouse oocytes grown with and without serum. Mol Reprod Dev 1992, 32: 33-40.
    Ermak G, Davies KJ. Calcium and oxidative stress: from cell signaling to cell death. Mol lmmunol 2002, 38(10): 713-72l.
    Faure S, Vigneron S, Doree M and Morin N. A member of the Ste20/pak family of protein kinases is involved in both arrest of Xenopus oocytes at G2/prophase of the first meiotic cell cycle and in the prevention of apoptosis. EMBO Journal 1997; 16: 5550-5561.
    Fierro L, Parekh AB. Fast calcium-dependent inactivation of calcium release-activated calcium current (CRAC) in RBL-1 cells. J Membr Biol 1999; 168: 9-17.
    Funahashi H, Cantley TC, Stumpf TT, Terlouw SL, Day B. Use of low-salt culture mediumwith elevated oocyte glutathione levels and enhanced male pronuclear formation after in vitro fertilization. Biol Reprod 1994; 51: 633-639.
    Furnus CC, de Matos DG, Moses DF. Cumulus expansions during in vitro maturation of bovine oocytes: Relationship level and its role on subsequent embryo development. Mol Reprod Dev 1998; 51: 76-83.
    Gabrielli BG, Roy LM, Maller JL. Requirment for cdk2 in cytostatic factor-mediated metaphase II arrest. Science 1993; 159: 1766-1769.
    Galvez A, Morales MP, Eltit JM, Ocaranza P, Carrasco L, Campos X, Sapag-Hagar M, Diaz-Araya G, and Lavandero S. A rapid and strong apoptotic process is triggered by hyperosmotic stress in cultured rat cardiac myocytes. Cell Tissue Res 2001; 304: 279-285.
    Gardiner CS, Reed DJ. Status of glutathione during oxidant-induced oxidative stress in the pre-implantation mouse embryo. Biol Reprod 1994; 51: 1307-1314.
    Geschi M, Takenouchi N, Yamauchi N, Nagai N. Effects of sodium pyruvate in nonserum maturation medium on maturation, fertilization, and subsequent development of bovine oocytes with or without cumulus cells. Biol Reprod 2002; 63: 1730-1734.
    Gonzales-Figueroa H, Gonzales-Molfino HM. Maturation of pig oocytes in vitro in a medium with pyruvate. Brazilian Journal of Medical and Biological Research 2005; 38: 869-872.
    Gordo AC, Kurokawa M, Wu H and Fissore RA Modifications of the Ca2+ release mechanisms of mouse eggs by fertilization and by the sperm factor. Molecular Human Reproduction 2002b; 8: 619-629.
    Gordo AC, Rodrigues P, Kurokawa M, Jellerette T, Exley GE, Warner C, Fissore R. Intracellular calcium oscillations signal apoptosis rather than activation in in vitro aged mouse eggs. Biol Reprod 2002, 66:1828-1837.
    Gordo AC, Wu H, He CL and Fissore RA. Injection of sperm cytosolic factor into mouse metaphase II oocytes induces different developmental fates according to the frequency of [Ca2+]i oscillations and oocyte age. Biology of Reproduction 2002a; 62: 1370-1379.
    Graier Hoebel BG, Paltauf-Doburzynska J, Kosmer GM. Efects of superoxide an ions on endothelial Ca sign aling pathways. A rterioscler Thromb Vasc BIOl 1998; 18:l470-l479.
    Green DR and Reed JC. Mitochondria and apoptosis. Science 1998, 281:1309-1312.
    Grover AK, Samson SE, Fomin VP. Peroxide inactivates calcium pumps in pig coronary artery. A rn J Physiol 1992; 263: H537-H543.
    Guérin P, Mouatassim S EI, Ménézo Y. Oxidative stress and protection against reactive oxygen species in the pre-implantation embryo and its surroundings. Hum Reprod Update 2001; 7: 175-189.
    Haccard O, Sarcevic B, Lewellyn A, Hartley R, Roy L, Izumi T, Erikson E, Maller JL. Induction of metaphase arrest in cleaving Xenopus embryos by MAP dinase. Science 1993; 262: 1262-1265.
    Halestrap AP, Kerr PM, Javadov S, and O’Toole A. Mitochondria and cell death. Biochem Soc Trans 2000; 28: 170-177.
    Halestrap AP, Kerr PM, Javadov S, and Woodfield KY. Elucidating the molecular mechanism of the permeability transition pore and its role in reperfusion injury of the heart. Biochim Biophys Acta 1998;1366: 79-94.
    Hammitt DG, Syrop CH, Van Voorhis BJ, Walker DL, Miller TM, Barud KM. Maturational asynchrony between oocyte cumulus-coronal morphology and nuclear maturity in gonadotropin-releasing hormone agonist stimulations. Fertil Steril 1993; 59: 375-381.
    Hashimoto N, Watanabe N, Furuta Y, Tamemoto H, Sagata N, Yokoyama M, Okazaki K, Nagayoshi M, Takeda N, Ikawa N, Aizawa S. Parthenogenetic activation of oocytes in c-mos-deficient mice. Nature 1994; 370: 68-71.
    Hoth M, Penner R. Calcium release-activated calcium current in rat mast cell. J Physiol 1993; 465:359-386.
    Huang JC, Yan LY, Lei ZL, Miao YL, Shi LH, Yang JW, Wang Q, Ouyang YC, Sun QY, Chen DY. Changes in histone acetylation during postovulatory aging of mouse oocyte. Biol Reprod 2007; 77:666-670.
    Igarashi H, Takahashi E, Hiroi M and Doi K. Aging-related changes in calcium oscillations in fertilized mouse oocytes. Mol Reprod and Dev 1997; 48: 383-390.
    Jabr RI, Cole WC. Alterations in electrical activity and membrane currents induced by intracellular oxygen-derived free radical stress in guinea pig ventricular myocytes. CircRes 1993; 72(6): 1229-1244.
    Jagtap JC, Chandele A, Chopde BA, Shastry P. Sodium pyruvate protects against H2O2 mediated apoptosis in human neuroblastoma cell line-SK-N-MC. J Chem Neuroanat 2003; 26: 109-118.
    Jiang S, Chow SC, Nicotera P and Orrenius S. Intracellular Ca2+ signals activate apoptosis in thymocytes: studies using the Ca2+-ATPase inhibitor thapsigargin. Experimental Cell Research 1994; 212: 84-92.
    Jones KT and Whittingham DG. A comparison of sperm- and IP3-induced Ca2+ release in activated and aging oocytes. Developmental Biology 1996; 178 229-237.
    Jones KT, Whittingham DG. Ionocycin, thapsigargin, ryanodine, and sperm induced Ca2+ release during meiotic maturation of mouse oocytes. J Biol Chem 1996; 178: 229-237.
    Kaneko M, Beam ish RE, Dhalla NS. Depression of heart sarcolemmal Ca2+-pump activity by oxygen free radicals. Am J Physiol 1989; 256: H368-H374.
    Kaneko M, Matsumoto Y, Hayashi H, Kobayashi A, Yamazaki N. Oxygen free radicals and calcium homeostasis in the heart. Mol Cell Biochem 1994; 135 (1): 99-108.
    Kang YH, Chung SJ, Park JHY, Kang IJ, Bünger R. Intramitochondrial pyruvate attenuates hydrogen peroxide-induced apoptosis in bovine pulmonary artery endothelium. Mol Cell Biochem 2001; 216: 27-46.
    Kashiwagi A, Nishio Y, Asahina T, Ikebuchi M, Harada N, Tanaka Y, Takahara N, Taki H, Obata T, Hidaka H, Saeki Y, and Kikkawa R. Pyruvate improves deleterious effects of high glucose on activation of pentose phosphate pathway and glutathione redox cycle in endothelial cells. Diabetes 1997; 46: 2088-2095.
    Kerr PM, Suleiman MS, and Halestrap AP. Reversal of permeability transition during recovery of hearts from ischemia and its enhancement by pyruvate. Am J Physiol Heart Circ Physiol 1999; 276: H496-H502.
    Khan S and O’Brien P. Rapid and specific efflux of glutathione before hepatocyte injury induced by hypoxia. Biochem Biophys Res Commun 1997; 238: 320-322.
    Kikuchi K, Naito K, Noguchi J, Shimada A, Kaneko H, Yamashita M, Aoki F, Tojo H, and Toyoda Y. Maturation/M-phase promoting factor: a regulator of aging in porcine oocytes. Biol Reprod 2000; 63: 715-722.
    Kim H, Schuetz AW. Regulation of parthenogenetic activation of metaphase II mouse oocytes by pyruvate. J Exp Zool 1991; 257:375-385.
    Kim JM, Liu HL, Tazaki M, Nagata M, Aoki F. Changes in histone acetylation during mouse oocyte meiosis. J Cell Biol 2003; 162:37-46.
    Kline D, Kline JT. Thapsigargin activates a calcium influx pathway in the unfertilized mouse egg and suppresses repetitive calcium transients in the fertilized egg. J Biol Chem 1992; 267: 17624-17630.
    Kroemer G, Zamzami N, Susin SA. Mitochondrial control of apoptosis. Immunol Today 1997; 18 (1): 44-50.
    Kruhlak MJ, Hendzel MJ, Fischle W, Bertos NR, Hameed S, Yang XJ, Verdin E, Bazett-Jones DP. Regulation of global acetylation in mitosis through loss of histone acetyltransferases and deacetylases from chromatin. J Biol Chem 2001; 276:38307-38319.
    Kubiak JZ, Weber M, Depennart H, Winston NJ, Maro B. The metaphase-II arrest in mouse oocytes is controlled through microtubule-dependent destruction of cyclin-B in the presence of CSF. EMBO J 1993; 12: 3773-3778.
    Kubiak JZ, Weber M, Depennart H, Winston NJ, Maro B. The metaphase-II arrest in miuse oocytes is controlled through microtubule-dependent destruction of cyclin-B in the presence of CSF. EMBO J 1993; 12: 3773-3778.
    Kuo TH, Kim HR, Zhu L, Yu Y, Lin HM and Tsang W. Modulation of endoplasmic reticulum calcium pump by Bcl-2. Oncogene 1998; 17: 1903-1910.
    Lee YJ, Kang IJ, Bünger R, Kang YH. Enhanced survival effect of pyruvate correlates MAPK and NF-κB activation in hydrogen peroxide-treated human endothelial cells. J Appl Physiol 2004; 96: 793-801.
    Lee YJ, Kang IJ, Bünger R, Kang YH. Mechanisms of pyruvate inhibition of oxidant-induced apoptosis in human endothelial cells. Microvasc Res 2003; 66: 91-101.
    Leese HJ, Barton AM. Pyruvate and glucose uptake by mouse ova and preimplantation. J Reprod Fertil 1984; 72:9-13.
    Liu L, Hammar K, Smith PJS, Inoue S and Keefe DL. Mitochondrial modulation of calcium signaling at the initiation of development. Cell Calcium 2001; 30: 423-433.
    Liu L, Trimarchi JR and Keefe DL. Involvement of mitochondria in oxidative stress-induced cell death in mouse zygotes Biology of Reproduction 2001; 62: 1745-1753.
    Longo FJ. Change in the zonae pellucidae and plasmalemmae of aging mouse eggs. Bio Reprod 1981; 25: 399-411.
    Longo FJ. Spontaneous activation of the hamster egg in vivo. In: Hess M (ed.), Electron Microscopic Concepts of Secretion–Ultrastructure of Endocrinal and Reproductive Organs. New York: John Wiley and Sons 1975: 35-51.
    Ma W, Zhang K, Hou Y, Li YH, Sun QY, Sun XF, Wang WH. Reduced expression of MAD2, BCL2, and MAP kinase activity in pig oocytes after in vitro aging are associated with defects in sister chromatid segregation duiring meiosis II and embryo fragmentation after activation. Biol Reprod 2005; 72: 373-383.
    Marchetti P, Decaudin D, Macho A, Zamzami N, Hirsch T, Susin SA, and Kroemer G. Redox regulation of apoptosis: impact of thiol oxidation status on mitochondrial function. Eur J Immunol 1997; 27: 289-296.
    Marston JH and Chang MC. The fertilizable life of ova and their morphology following delayed insemination in mature and immature mice. Journal of Experimental Zoology 1964; 155: 237-252.
    Martinez F, Rienzi L, Iacobelli M, Ubaldi F, Mendoza C, Greco E and Tesarik J. Caspase activity in preimplantation human embryos is not associated with apoptosis. Human Reproduction 2002; 17: 1584-1590.
    Masui Y. The role of cytostatic factor (CSF) in the control of oocyte cell cycles: A summary of 20 years of study. Dev Growth Differ 1991; 33: 543-551.
    Maulik N, Sasaki H, Addya S, and Das DK. Regulation of cardiomyocyte apoptosis by redox-sensitive transcription factors.FEBS Lett 2000; 485: 7-12.
    Meister A. Selective modification of glutathione metabolism. Science 1983; 220: 472-477.
    Merchant H, Chang MC. An electron microscopic study of mouse eggs matured in vivo and in vitro. Anat Rec 1971; 171: 21-38.
    Miquel J, Economos AC, Fleming J, Johnson JE Jr. Mitochondrial role in cell aging. Exp Gerontol 1980; 15: 575-591.
    Miyazaki S, Hashimoto N, Yoshimoto Y, Kishimoto T, Igusa Y, Hiramoto Y. Temporal andspatial dynamics of the periodic increase in intracellar free calcium at fertilization of golden hamster eggs. Dev Biol 1986; 118:259-267.
    Mongan PD, Capacchione J, Fontana JL, West S, and Bunger R. Pyruvate improves cerebral metabolism during hemorrhagic shock. Am J Physiol Heart Circ Physiol 2001; 281: H854-H864.
    Mongan PD, Capacchione J, West S, Karaian J, Dubois D, Keneally R, and Sharma P. Am J Physiol Heart Circ Physiol 2002; 283: 1643-1644.
    Mongan PD, Fontana JL, Chen R, and Bunger R. Intravenous pyruvate prolongs survival during hemorrhagic shock in swine. Am J Physiol Heart Circ Physiol 1999; 277: H2253-H2263.
    Mongan, PD, Capacchione J, West S, Karaian J, Dubois D, Keneally R, Sharma P. Pyruvate improves redox status and decreases indictors of hepatic apoptosis duing hemorrhagic shock in swine. Am J Physiol Heart Circ Physiol 2002; 283: H1634-H1644.
    Monteiro, H.P., Ivaschenko, Y., Fisher, R. and Stern, A. Inhibition of protein tyrosine phosphatase activity by diamide is reversed by epidermal growth factor in fibroblasts. FEBS Leu 1991; 295: 146-148.
    Morales H, Tilquin PJ, Rees JF et al. Pyruvate prevents peroxide-induced injury of in vitro preimplantation bovine embryos. Mol Reprod Dev 1999, 52: 149-157. Muallem S. Calcium signaling: Pyruvate and CRAC meet at the crossroads. Curr Biol 2007; 17: R549-R551.
    Mukhopadhaya S., Mondal A., and Poddar M. K. Chronic administration of caffeine: effect on the activities of hepatic antioxidant enzymes of Ehrlich ascites tumor-bearing mice. Indian J. Exp Biol 2003; 41: 283-289.
    Naito K, Dean F P, Toyoda Y. Comparison of histone HI kinase activity during meiotic maturation between two types of porcine oocytes matured in different media in vitro. Biology of Reproduction 1992; 47: 43-47.
    Natsuyama S, Noda Y, Yamashita M et al. Superoxide dismutase and thioredoxin restore defective p34cdc2 kinase activation in mouse twocell block. Biochem Biophys Ada 1993; 1176: 90-94.
    Niknahad H, Khan S, and O’Brien PJ. Hepatocyte injury resulting from the inhibition ofmitochondrial respiration at low oxygen concentrations involves reductive stress and oxygen activation. Chem Biol Interact 1995; 98: 27-44.
    Nurse P. Universal control mechanism regulating the onset of M-phase. Nature 1990; 344: 503-508.
    O’Donnell-Tormey J, Nathan CF, Lanks K, DeBoer CJ, Harpe J de la. Secretion of pyruvate. An antioxidant defense of mammalian cells. J Exp Med 1987; 165: 500-514.
    O’Fallon JV, Wright RW Jr. Pyruvate revisited: a nonmetabolic role for pyruvate in preimplantation embryo development. Theriogenology 1995; 43: 288.
    O’Keefe SJ, Wolfes H, Kiessling AA, Cooper GM. Micro-injection of antisense c-mos oligonucleotides prevents meiosis II in the maturing mouse egg. Proc Matl Acad Sci LSA 1989; 86: 7038-7042.
    Oltvai ZN, MIlliman CL, Korsmeyer SJ. BCL-2 heterodimerizes in vitro with a conserved homology, Bax, that accelerates programmed cell death. Cell 1993; 74:609-619.
    Ozil JP. The parthenogenetic development of rabbit oocytes after repetitive pulsatile electrical stimulation. Development 1990; 109:117-127.
    Parekh AB, Putney JWJ. Store-operated calcium channels. Physiol Rev 2005; 85: 757-810.
    Perez GI, Trobovich AM, Gosden RG and Tilly JL. Mitochondria and the death of oocytes. Nature 2000; 403: 500-501.
    Perreault SD, Barbee RR, Slott VI. Importance of glutathione in the acquisition and maintenance of sperm nuclear decondensing activity in maturing hamster oocytes. Dev Biol 1988; 125: 181-186.
    Pias EK, Aw TY. Apoptosis in mitotic competent undifferentiated cells is induced by cellular redox imbalance independent of reactive oxygen species production. FASEB J 2002; 16 (8) : 781-790.
    Pinton P, Ferrari D, Magalhaes P, Schulze-Osthoff K, Di Virgilio F, Pozzan T and Rizzuto R. Reduced loading of intracellular Ca2+ stores and downregulation of capacitative Ca2+ influx in Bcl-2-overexpressing cells. Journal of Cell Biology 2000; 148: 857-862.
    Ramakrishnan N, Chen R, McClain DE, Bünger R. Pyruvate prevents hydrogen peroxide-induced apoptosis. Free Radic Res 1998; 29: 283-295.
    Raz T, Skutelsky E. The MAP kinase cascade: its role in Xenopus oocytes, eggs and embryos,Prog. Cell Cycle Res 1995; 52: 295-303.
    Rieger D, Loskutoff NM. Changes in the metabolism of glucose, pyruvate, glutamine and glycine during maturation of cattle oocytes in vitro. J Reprod Fertil 1994; 100: 257-256.
    Rojanasakul Y, Wang L, Hoffrnan AH, Shi X, Dalai NS, Banks DE, Ma JK. Mechan isms of hydroxyl flee radica1 induced cellular injury and calcium overloading in alveolar macrophages. Am J Respir Cell Mol Biol l993; 8(4): 377-383.
    Roved A, Coassin M, Maiorino M, Zamburlini A, van Ains, terdam FT, Ratti E, Ursini F. Efect of hydrogen peroxide on calcium homeostasis in smooth muscle cells Archives of Biochemistry& Biophysics 1992; 297(2): 265-270.
    Sagata N. Meiotic metaphase arrest in animal oocytes: Its mechanisms and biologicl significance. Trends Cell Biol 1996; 6: 22-28.
    Schafer FQ and Buettner GR. Redox environment of the cell as viewed through the redox state of the glutathione disulfide/ glutathione couple. Free Radic Biol Med 2001; 30: 1191-1212.
    Scherer NM, Deamer DW. Oxidative stress impairs the function of sarcoplasmic reticulum by oxidation of sulfhydryl groups in the Ca2+-ATPase. A rch Biochem Biophys 1986; 246: 589-601.
    Schmidt, H. H., and Walter, U. NO at work. Cell 1994, 78: 919-925.
    Smith JJ, Evans EK, Murakami M, Moyer MB, Moseley MA, Vande Woude G and Kornbluth S . Wee1-regulated apoptosis mediated by the Crk adaptor protein in Xenopusegg extracts. Journal of Cell Biology 2000; 151: 1391-1400.
    Soboloff J and Berger SA. Sustained ER Ca2+ depletion suppresses protein synthesis and induces activation-enhanced cell death in mast cells. Journal of Biological Chemistry 2002; 277: 13812-13820.
    Soldani C, Lazze MC, Bottone MG, Tognon G, Biggiogera M, Pellicciari CE, and Scovassi AI. Poly(ADP-ribose) polymerase cleavage during apoptosis: when and where? Exp Cell Res 2001; 269: 193-201.
    Souza M, Barros A, Silva J and Tesarik J. Developmental changes in calcium content of ultrastructurally distinct subcellular compartments of preimplantation human embryos. Molecular Human Reproduction 1997; 3: 83-90.
    Stumpf T T, Funahashi H, Terlouw S L, Day B N. Histone Hl kinase activity after electrical activation of in vitro matured porcine oocytes. Journal of Animal Science 1994; 72 (suppl. 1): 74.
    Sullivan, S.G., Chiu, D.T.Y., Errasfa, M. et al. Effects of H2O2 on protein tyrosine phosphatase activity in HER14 cells. Free Rad Biol Med 1994; 16: 399-403.
    Sutovsky P, Schatten G Depletion of glutathione during bovine oocyte maturation reversibly blocks the decondensation of the male pronucleus and pronucleus apposition during fertilization. Biol Reprod 1997; 56:1503-1512.
    Swaan K, Ozil JP. Dynamics of the calcium signal that triggers mammalian egg activation. Int Rev Cytol 1994; 152: 182-222.
    Szalai G, Krishnamurthy R and Hajnóczky G. Apoptosis driven by IP3-linked mitochondrial calcium signals. EMBO Journal 1999; 18: 6349-6361.
    Szollosi D. Morphological changes in mouse eggs due to aging in the Fallopian tube. Am J Anat 1971; 130: 209-226.
    Takahashi T, Saito H, Hiroi M, Doi K and Takahashi E. Effects of aging on inositol 1,4,5-triphosphate-induced Ca2+ release in unfertilized mouse oocytes Mol Reprod Dev 2000; 55: 299-306.
    Takahashi T, Takahashi E, Igarashi H, Tezuka N, Kurachi H. Impact of oxidative stress in aged mouse oocytes on calcium oscillations at fertilization. Mol Reprod Dev 2000; 55:299-306.
    Tan JH. Studies on the goat egg. A Ph.D thesis at the Northeast Agricultural College, Harbin PR China 1988.
    Tarín J J. Potential effects of age-associated oxidative stress on mammalian oocytes/embryos. Mol Hum Reprod 1996; 2: 717-724.
    Tarin JJ, Albalá-Pérez S, Aguilar A, Minarro J, Hermenegildo C and Cano C. Long-term effects of postovulatory aging of mouse oocytes on offspring: a two-generational study. Biology of Reproduction 1999; 61: 1347-1355.
    Tarin JJ, Perez-Albala S, Cano A. Consequences on offspring of abnormal function in ageing gametes. Hum Reprod Update 2000; 6: 532-549.
    Tarin JJ, Ten J, Vendrell FJ and Cano A. Dithiothreitol prevents ageassociated decrease inoocyte/conceptus viability in vitro. Human Reproduction 1998; 13: 381-386.
    Tarín JJ, Ten J, Vendrell FJ, Cano A. Dithiothreitol prevents age-associated decrease in oocyte/conceptus viability in vitro. Hum Reprod 1998; 13: 381-386.
    Tejero-Taldo MI, Caffrey JL, Sun J, and Mallet RT. Antioxidant properties of pyruvate mediate its potentiation of beta-adrenergic inotropism in stunned myocardium. J Mol Cell Cardiol 1999; 31: 1863-1872.
    Tejero-Taldo MI, Caffrey JL, Sun J, and Mallet RT. Antioxidant properties of pyruvate mediate its potentiation of beta- adrenergic inotropism in stunned myocardium. J Mol Cell Cardiol 1999; 31: 1863-1872.
    Thomenius MJ, Distelhorst CW. Bcl-2 on the endoplasmic reticulum: protecting the mitochondria from a distance. J cell Sci 2003; 116:4493-4499.
    Trump BF and Berezesky IK. Calcium-mediated cell injury and cell death. FASEB Journa 1995; l9: 219-228.
    Trump BF, Berezesky IK. Calcium-mediated cell injury and cell death. FSSEB Journal 1995; 9: 219-228.
    Van Blerkom J, Davis PW and Lee J. ATP content of human oocytes and the developmental potential and outcome after in-vitrofertilization and embryo transfer. Human Reproduction 1995; 10: 415-424.
    Vander Heiden MG, Thompson CB. BCL-2 proteins: regulators of apoptosis or of mitochondrial homeostasis? Nat Cell Biol 1999; 1:209-216.
    Wang TG, Gotoh Y, Jennings MH, Rhoads CA, and Aw TY. Lipid hydroperoxide-induced apoptosis in human colonic CaCo-2 cells is associated with an early loss of cellular redox balance. FASEB J 2000; 14: 1567-1576.
    Wang TG, Gotoh Y, Jennings MH, Rhoads CA, and Aw TY. Lipid hydroperoxide-induced apoptosis in human colonic CaCo-2 cells is associated with an early loss of cellular redox balance. FASEB J 2000; 14: 1567-1576.
    Wang X. The expanding role of the mitochondria in apoptosis. Genes and Development 2001; 15: 2922-2933.
    Weil M, Jacobson MD, Coles HS, Davies TJ, Gardner RL, Raff KD and Raff MC. Constitutive expression of the machinery for programmed cell death. Journal of CellBiology 1996; 133: 1053-1059.
    Wilding M, Dale B, Marino M, di Mateo L, Alviggi C, Pissature ML, Lombardi L and De Placido G. Mitochondrial aggregation patterns and activity in human oocytes and preimplantation embryos. Human Reproduction 2001; 16: 909-917.
    Xu N, Luo KQ, Chang DC. Ca2+ signal blockers can inhibit M/A transition in mammalian cells by interfering with the spindle checkr)oint. Biochem Biophys Res Commun 2003; 306(3): 737-745.
    Xu Z, Abbott A, Kopf GS, Schultz RM, Ducibella T. Spontaneous activation of ovulated mouse eggs: time-dependent eddects on M-phase exit, cortical granule exocytosis, maternal messenger ribonucleic acid recruitment, and inositol 1,4,5-trisphosphate sensitivity. Biol Reprod 1997; 57: 743-70.
    Yanagimachi R, Chang MC. Fertilizable life of glden hamster ova and their morphological changes at the time of losing fertilizability. J Exp Zool 1961; 148: 185-197.
    Yang Z, Zingarelli B, and Szabo C. Effect of genetic disruption of poly (ADP-ribose) synthetase on delayed production of inflammatory mediators and delayed necrosis during myocardial ischemia-reperfusion injury. Shock 2000; 13: 60-66.
    Yoshida M, Ishigaki K, Nagai T, Chikyu M, Pursel VG. Glutathione concentration during maturation and after fertilization in pig oocytes: Relevance to the ability of oocytes to form male pronucleus. Biol Reprod 1993; 49: 89-94.
    Yoshida M, Kijima M, Akita M, Beppu T. Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A. J Biol Chem 1990; 265: 17174-17179.
    Zuelke KA, Jeffay SC, Zucker RM, Perreault SD. Glutathione (GSH) concentrations vary with the cell cycle in maturing hamster oocytes, zygotes, and pre-implantation stage embryos. Mol Reprod Dev 2003; 64: 106-112.
    Zuelke KA, Jones DP, Perreault SD. Glutathione oxidation is associates with altered microtubule function and disrupted fertilization in mature hamster oocytes. Biol Reprod 1997; 57: 1413-1420.
    Zweifach A, Lewis RS. Rapid inactivation of depletion-activated calcium current (ICRAC) due to lacal calcium feedback. J Gen Physiol 1995; 105: 209-226.

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