期刊文献+

抗坏血酸、表皮生长因子和促卵泡素对绵羊卵巢皮质体外培养的影响 被引量:1

Effect of ascorbic acid, epidermal growth factor and follicle stimulating hormone on in vitro culture of sheep ovarian cortical tissue
原文传递
导出
摘要 本研究旨在评估抗坏血酸(VC)、表皮生长因子(EGF)、促卵泡素(FSH)对绵羊原始卵泡体外培养的影响以及它们之间的相互关系。实验按照2×2×2因子试验设计分为8组,分别为:MEM(对照组),MEM+VC(50μg/mL),MEM+EGF(100ng/mL),MEM+FSH(50ng/mL),MEM+VC+EGF,MEM+VC+FSH,MEM+EGF+FSH,MEM+VC+EGF+FSH。在培养0(未培养对照组)、2、6、12d后,对培养的卵巢皮质薄片进行组织学和增殖细胞核抗原(PCNA)检测以及透射电镜(TEM)观察。结果表明,与未培养组(发育卵泡比例15.4%±1.9%,正常卵泡比例88.2%±4.6%)比较,所有培养组中发育卵泡比例显著增加(P<0.05),正常卵泡比例下降(P<0.05)。培养12d后,与对照组(卵泡直径(34.5±3.3)μm,卵泡存活比例(38.9%±3.9%))比较,MEM+VC+FSH和MEM+EGF+FSH组中卵泡直径(分别为(39.7±3.4)μm和(42.5±5.1)μm)和卵泡存活比例(分别为58.5%±4.3%和59.3%±3.7%)都显著提高(P<0.05);各处理组中,培养12d后,MEM+VC+EGF组中发育卵泡比例(49.3%±3.2%)和卵泡直径((32.3±2.3)μm)最低,颗粒细胞PCNA阳性卵泡比例(26.4%±1.2%)也最少,而MEM+VC+EGF+FSH组中卵泡存活率(59.7%±6.1%)和卵泡直径((42.5±5.1)μm)都显著增加(P<0.05),颗粒细胞PCNA(43.5%±4.1%,P<0.05)表达增加。电镜结果表明,VC+EGF+FSH组能够维持与正常卵泡类似的超微结构,而在MEM和MEM+VC+EGF组却显示不同程度的退化特征。本研究结果提示在培养中联合添加VC与EGF抑制卵泡的发育和生长,而联合添加VC、EGF和FSH可能是促进绵羊原始卵泡体外激活和生长,维持卵泡存活以及结构完整的最有效的处理手段之一。 In this study,we evaluated the effects of ascorbic acid (VC),epidermal growth factor (EGF) and follicle stimulating hormone (FSH) on in vitro culture of sheep ovarian cortical tissue.Using 2×2×2 factor experimental design,we cultured sheep ovarian cortex fragments in 8 media with MEM (control),MEM+VC (50 μg/mL),MEM +EGF (100 ng/mL),MEM+FSH (50 ng/mL),MEM+VC+EGF,MEM+VC+FSH,MEM+EGF+FSH,MEM+VC+EGF+FSH.After 0 (non-cultured control),2,6,12 days of culture,the pieces of ovarian cortex were proceed to histological and proliferating cell nuclear antigen (PCNA) examination,or observed by transmission electron microscopy (TEM).The percentages of developing follicles were increased (P〈0.05) and the percentages of healthy follicles were reduced (P〈0.05).When compared to the MEM group,the addition of FSH with VC or EGF promoted a significant increase of follicles diameter and follicles survival rate (P〈0.05),and stimulated the proliferation of granulosa cells.After 12 days of culture,medium supplemented with MEM+VC+EGF resulted the lowest proportion of developing follicles (49.3%±3.2%),follicles diameter((32.3±2.3) μm),follicles survival rate (41.6%±3.1%) and the proportion of PCNA stained follicles (26.4%±1.2%,P〈0.05).In contrast,MEM+VC+EGF+FSH resulted the highest follicles diameter ((42.5±5.1) μm),follicles survival rate (59.7%±6.1%) and proportion of PCNA stained follicles (43.5%±4.1%,P〈0.05).Ultrastructural analysis confirmed the integrity of follicles cultured in VC+EGF+FSH group,while follicles cultured in MEM+VC+EGF groups showed more degeneration characters.In conclusion,the addition of VC and EGF to culture medium inhibited follicular development,VC+EGF+FSH was the most effective treatment to maintain follicular integrity and promote sheep primordial follicular activation and growth during in vitro culture.
出处 《生物工程学报》 CAS CSCD 北大核心 2010年第6期744-752,共9页 Chinese Journal of Biotechnology
基金 国家科技支撑项目(Nos.2008ADB2B05-10 2008ADB2B010-5)资助~~
关键词 绵羊 原始卵泡培养 抗坏血酸 促卵泡素 表皮生长因子 sheep ovarian tissue ascorbic acid follicle stimulating hormone epidermal growth factor
  • 相关文献

参考文献27

  • 1Markstrom E, Svensson E, Shao R, et al. Survival factors regulating ovarian apoptosis--dependence on follicle differentiation. Reprod, 2002, 123: 23-30.
  • 2Greenwald GS, Roy SK. Follicular development and its control//Knobil E, Neill JD, eds. Physiology of Reproduction. New York: Raven Press, 1994: 629-725.
  • 3Silva JR, Hurk R, Matos MHT, et al. Influences of FSH and EGF on primordial follicles during in vitro culture of caprine ovarian cortical tissue. Theriogenology, 2004, 61: 1691-1704.
  • 4Matos MHT, Lima-Verde IB, Luque MCA, et al. Essential role of follicle stimulating hormone in the maintenance of caprine preantral follicle viability in vitro. Zygote, 2007, 15: 173-182.
  • 5Saha S, Shimizu M, Geshi M, et al. In vitro culture of bovine preantral follicles. Anim Reprod Sci, 2000, 63: 27-39.
  • 6Reeka N, Berg FD, Brucker C. Presence of transforming growth factor alpha and epidermal growth factor in human ovarian tissue and follicular fluid. Hum Reprod, 1998, 13: 2199-2205.
  • 7Qu JP, Godin PA, Nisolle M, et al. Distribution of epidermal growth factor receptor expression of primordial follicles in human ovarian tissue before and after cryopreservation. Hum Reprod, 2000, 15:302-310.
  • 8Garner K, Wang J, Roy SK. Spatiotemporal expression of epidermal growth factor receptor messenger RNA and protein in the hamster ovary: follicle stage-specific differential modulation by follicle stimulating hormone, luteinizing hormone, estradiol, and progesterone. Biol Reprod, 2002, 67: 1593-1604.
  • 9Wandji SA, Srsen V, Nathanielsz, et al. Initiation of growth of baboon primordial follicles in vitro. Hum Reprod, 1997, 12: 1993-2001.
  • 10Morbeck DE, Flowers WL, Britt JH, et al. Response of porcine granulosa cells isolated from primary and secondary follicles to FSH, 8-bromo-cAMP and epidermal growth factor in vitro. ReprodFertil, 1993, 99: 577-584.

同被引文献11

  • 1ECR Leonel,V Bento‐Silva,KS Ambrozio,HS Luna,EV Costa e Silva,CESN Zúccari.Methods for Equine Preantral Follicles Isolation: Quantitative Aspects[J].Reprod Dom Anim.2013(6)
  • 2Evelyn R. Andrade,Robert van den Hurk,Lívia A. Lisboa,Mariana F. Hertel,Fabiana A. Melo-Sterza,Kleber Moreno,Ana Paula F. R. L. Bracarense,Fernanda C. Landim-Alvarenga,Marcelo M. Seneda,Amauri A. Alfieri.Effects of ascorbic acid on in vitro culture of bovine preantral follicles[J].Zygote.2012(4)
  • 3Shi Ying Jin,Lei Lei,Ariella Shikanov,Lonnie D. Shea,Teresa K. Woodruff.A novel two-step strategy for in vitro culture of early-stage ovarian follicles in the mouse[J].Fertility and Sterility.2010(8)
  • 4R. Rossetto,I.B. Lima-Verde,M.H.T. Matos,M.V.A. Saraiva,F.S. Martins,L.R. Faustino,V.R. Araújo,C.M.G. Silva,K.P.O. Name,S.N. Báo SN,C.C. Campello,J.R. Figueiredo,H. Blume.Interaction between ascorbic acid and follicle-stimulating hormone maintains follicular viability after long-term in vitro culture of caprine preantral follicles[J].Domestic Animal Endocrinology.2009(2)
  • 5Seung Tae Lee,Mun Hwan Choi,Eun Ju Lee,Seung Pyo Gong,Mi Jang,Sang Hyun Park,Hyang Jee,Dae Yong Kim,Jae Yong Han,Jeong Mook Lim.Establishment of autologous embryonic stem cells derived from preantral follicle culture and oocyte parthenogenesis[J].Fertility and Sterility.2008(5)
  • 6Douglas T. Carrell,Lihua Liu,Ivan Huang,C. Matthew Peterson.Comparison of maturation, meiotic competence, and chromosome aneuploidy of oocytes derived from two protocols for in vitro culture of mouse secondary follicles[J].Journal of Assisted Reproduction and Genetics (-).2005(9-10)
  • 7Masaki Iwamoto,Akira Onishi,Dai-ichiro Fuchimoto,Tamas Somfai,Kumiko Takeda,Takahiro Tagami,Hirofumi Hanada,Junko Noguchi,Hiroyuki Kaneko,Takashi Nagai,Kazuhiro Kikuchi.Low oxygen tension during in vitro maturation of porcine follicular oocytes improves parthenogenetic activation and subsequent development to the blastocyst stage[J].Theriogenology.2004(5)
  • 8YTao,BZhou,GXia,FWang,ZWu,MFu.Exposure to L‐Ascorbic Acid or α‐Tocopherol Facilitates the Development of Porcine Denuded Oocytes from Metaphase I to Metaphase II and Prevents Cumulus Cells from Fragmentation[J].Reproduction in Domestic Animals.2004(1)
  • 9J.H. Kim,K.S. Park,H.B. Song,S.S. Chun.A Simple Isolating Method of Preantral Follicles from Mouse Ovaries[J].Fertility and Sterility.2000(3)
  • 10丁婷,罗爱月,杨书红,赖志文,卢运萍,马丁,王世宣.小鼠腔前卵泡不同分离方法的比较[J].中国现代医学杂志,2010,20(5):695-698. 被引量:5

引证文献1

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部