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1.
目前 ,动物腔前卵泡的体外培养正日益受到重视 ,并已取得了较大进展 ,已建立的培养体系可成功地使腔前卵泡发育到有腔阶段 ,猪、山羊等已可实现腔前卵泡卵母细胞体外成熟 ,体外受精并发育至囊胚阶段。但有关腔前卵泡体外成熟的机制仍不明了。本文通过对体内发育与体外培养之卵泡及其卵母细胞超微结构进行比较 ,从微细结构上客观评定体外培养卵泡的形态、活力、代谢状况及功能完整性 ,界定体外生长卵泡所处发育阶段 ,从而为确立和完善腔前卵泡体外培养体系并最终选择高质量的卵母细胞进行体外受精提供可靠的理论依据。1 体内发育卵泡及其卵…  相似文献   

2.
哺乳动物腔前卵泡卵母细胞的体外培养   总被引:1,自引:1,他引:0  
阐明哺乳动物卵泡体内发生的一般模式,回顾腔前卵泡体外培养的研究历史,着重论述腔前卵泡的获取及鉴定标准,常用的培养体系和影响腔前卵泡体外发育的多种因素。  相似文献   

3.
猪腔前卵泡体外培养研究进展   总被引:1,自引:1,他引:0  
哺乳动物卵巢中有数量丰富的腔前卵泡,腔前卵泡体外发育的研究,对于揭示卵子发生和卵泡发育的内在规律有重要意义,并可以最大限度利用卵巢资源促进动物繁殖,保护濒临灭绝物种及人类生殖健康。猪腔前卵泡自开始研究以来,已取得了很大的进展。作者简要阐述了猪腔前卵泡培养方法、培养条件的研究进展及其体外培养技术存在的问题和发展前景。  相似文献   

4.
哺乳动物卵巢中绝大多数卵母细胞以无腔形式存在,有腔卵泡所占比例很少。通过建立腔前卵泡的培养体系,获取大量的具有成熟和受精能力的卵母细胞,将极大地促进体外受精、核移植等胚胎工程技术的发展,并有利于研究卵泡和卵母细胞的发育规律。  相似文献   

5.
刘海军 《猪业科学》2001,18(1):30-31
哺乳动物卵巢中绝大多数卵母细胞以无腔形式存在,有腔卵泡所占比例很少。通过建立腔前卵泡的培养体系,获取大量的具有成熟和受精能力的卵母细胞,将极大地促进体外受精、核移植等胚胎工程技术的发展,并有利于研究卵泡和卵母细胞的发育规律。  相似文献   

6.
牛腔前卵泡在无血清下体外培养 1 5d。超微结构研究显示 :培养前腔前卵泡卵母细胞微绒毛短小 ,分布均匀 ;培养 6d时 ,微绒毛略变粗长 ,但数量减少 ;培养 1 5d时 ,微绒毛增多 ,变长 ,斜向或垂直插入已经形成的透明带中。微绒毛的存在和变化表明腔前卵泡在该无血清体系中发育正常。  相似文献   

7.
哺乳动物卵泡发育过程中的超微结构研究进展   总被引:1,自引:0,他引:1  
通过对体内发育与体外培养卵泡及其卵母细胞超微结构进行比较。从微细结构上客观评定体外培养卵泡的形态,活力,代谢状况及功能完整性,界定体外生长卵泡所处发育阶段。从而为确立和完善腔前卵泡体外培养体系提供可靠的理论依据。  相似文献   

8.
哺乳动物腔前卵泡的研究进展   总被引:1,自引:0,他引:1  
哺乳动物的卵巢中,含有数万个卵泡.其中绝大部分为原始卵泡、初级卵泡和次级卵泡等腔前卵泡。然而能发育到成熟并排卵的卵泡为数甚少,约99.9%的卵泡在腔前卵泡阶段闭锁、退化,这无疑是动物遗传和育种资源的极大损失。目前,卵母细咆是休外受精胚胎移植、性别控制、胚胎分割、动物克隆和转基凶等胚胎生物技术研究和开发必不可少的材料,卵母细胞来源匮乏成为制约这些技术研究进展的主要因素,因此卵巢腔前卵泡的开发无疑是解决这一难题的有效途径。本文介绍了腔前卵泡研究的历史和现状以及最新的研究情况.目的是为有关的研究工作提供有益的启示和参考。  相似文献   

9.
透射电镜下,简易机械法分离得到的腔前卵泡有1~3层颗粒细胞,相邻颗粒细胞间存在明显而广泛的间隙连接,卵泡基膜完整,外无卵泡膜。培养过程中超微结构的变化与体内发育腔前卵泡类似。培养6d时观察到颗粒细胞增殖现象,培养15d时,个别卵泡的内膜细胞开始形成。超微结构研究结果表明,本培养体系适于小腔前卵泡的体外培养。  相似文献   

10.
哺乳动物腔前卵泡体外培养研究进展   总被引:2,自引:0,他引:2  
哺乳动物腔前卵泡的体外培养可充分挖掘优良母畜潜在的遗传和繁殖潜力,为体外胚胎生产提供大量的卵母细胞来源,因而正日益受到人们的重视。本文就哺乳动物腔前卵泡的体外发育中的培养系统、培养方法,培养形式以及影响其体外发育的因素等几个方面进行了阐述。  相似文献   

11.
In vitro Follicle Growth: Achievements in Mammalian Species   总被引:4,自引:0,他引:4  
The exact mechanisms regulating in vivo folliculogenesis in mammalians have only been partly unravelled. Some processes, such as the initiation of growth of primordial follicles are still poorly understood. This increases the difficulty to culture follicles in vitro as the primordial follicles will be the ultimate starting material for culture.
There are important species differences in regulation and timing of maturation, which makes it difficult to transpose techniques.
Only in the mouse model, live pups were born when primordial or early preantral follicles were cultured entirely in vitro . Although no systems are as yet permitting complete in vitro culture of early follicle stages in large animals or humans, parts of folliculogenesis have been successfully reproduced in vitro . This review summarizes achievements of the last years in follicle culturing starting off at several stages of development.
Future applications of in vitro follicle culture include fertility preservation for humans, preservation of rare animal species and creation of oocyte banks for research.  相似文献   

12.
In this study, the expressions of VEGF in dog follicles were detected by immunohistochemistry and the effects of VEGF treatment on the primordial to primary follicle transition and on subsequent follicle progression were examined using a dog ovary organ culture system. The frozen‐thawed canine ovarian follicles within slices of ovarian cortical tissue were cultured for 7 and 14 days in presence or absence of VEGF. After culture, the ovaries were fixed, sectioned, stained and counted for morphologic analysis. The results showed that VEGF was expressed in the theca cells of antral follicles and in the granulosa cells nearest the oocyte in preantral follicle but not in granulosa cells of primordial and primary follicles; however, the VEGF protein was expressed in CL. After in vitro culture, VEGF caused a decrease in the number of primordial follicles and concomitant increase in the number of primary follicles that showed growth initiation and reached the secondary and preantral stages of development after 7 and 14 days. Follicular viability was also improved in the presence of VEGF after 7 and 14 days in culture. In conclusion, treatment with VEGF was found to promote the activation of primordial follicle development that could provide an alternative approach to stimulate early follicle development in dogs.  相似文献   

13.
The present study aimed to evaluate the effect of three culture systems on caprine primordial follicle activation in vitro: follicles cultured either in the isolated form within alginate (Isolated follicles + Alginate treatment), or enclosed in ovarian tissue (in situ), with or without alginate (Fragment + Alginate, and Fragment alone treatments, respectively). After culture, the Isolated follicles + Alginate treatment presented a percentage of morphologically normal follicles (MNF) similar to both the non-cultured control and the Fragment Alone treatments. Nevertheless, Fragment + Alginate treatment showed a significant reduction in the number of MNF when compared to the other treatments. Regarding follicle development, our results showed that regardless of the alginate, the presence of ovarian tissue limited primordial follicle activation during in vitro culture. Remarkably, the Isolated primordial follicle + Alginate treatment was the only one that significantly promoted follicle activation and increased both follicle and oocyte diameters during IVFC, pointing out a higher cell proliferation. In conclusion, the presence of ovarian tissue with or without alginate limited follicle development (activation) after culture. Nevertheless, when primordial follicles were isolated and encapsulated in alginate they presented suitable survival rates, higher rates of follicle activation and continued to grow throughout the culture period.  相似文献   

14.
The vanadate‐derivative dipotassium bisperoxo (5‐hydroxy‐pyridine‐2‐carboxylic) oxovanadate (V) (bpV(HOpic)), a pharmacological inhibitor of phosphatase and tensin homolog (PTEN), has been used in ovarian follicle culture systems for activation of follicular growth in vitro and suggested to be responsible for primordial follicle survival through indirect Akt activation. For pig ovarian tissue, it is still not clear which culture medium needs to be used, as well as which factors and hormones could influence follicular development; this also applies to bpV(HOpic) exposure. Therefore, ovarian cortical strips from pigs were cultured in 1 µM bpV(HOpic) (N = 24) or control medium (N = 24) for 48 hr. Media were then replaced with control medium and all tissue pieces incubated for additional 4 days. The strips were embedded in paraffin for histological determination of follicle proportions at the end of the culture period and compared to histological sections from tissue pieces without cultivation, which had been embedded right after preparation; comparison of healthy follicles for each developmental stage was performed to quantify follicle survival and activation. After 6‐day culture, follicle activation occurred in tissue samples from both cultured groups but significantly more follicles showed progression of follicular development in the presence of 1 µM bpV(HOpic). The amount of non‐vital follicles was not significantly increased during cultivation. BpV(HOpic) affects pig ovarian follicle development by promoting the initiation of follicle growth and development, similar as in rodent species and humans.  相似文献   

15.
促卵泡素对鸡等级前卵泡细胞发育的影响   总被引:2,自引:0,他引:2  
实验研究了鸡等级前卵泡颗粒细胞和膜细胞的发育及促卵泡素(FSH)对其增殖的调控作用。形态学观察显示小白卵泡只有1层颗粒细胞,大白卵泡出现2层颗粒细胞,而小黄卵泡和大黄卵泡中则有多层颗粒细胞。结果表明:卵泡颗粒细胞和膜细胞的密度和细胞层厚度随着卵泡发育的等级而增加。卵泡体外悬浮培养表明,FSH显著刺激小黄卵泡和大黄卵泡中颗粒细胞的增殖,但对膜细胞无显著促增殖作用。由此推测,FSH通过刺激颗粒细胞的增殖促使等级前卵泡进入等级发育。  相似文献   

16.
Characteristics of Ovarian Follicle Development in Domestic Animals   总被引:4,自引:0,他引:4  
In most domestic animals the later stages of follicle development occurs in a wave‐like pattern during oestrous cycles (cattle, sheep, goats, horses and buffalo) or periods of reproductive activity (llamas and camels). A follicle wave is the organized development of a cohort of gonadotrophin‐dependent follicles all of which initially increase in size, but most of which subsequently regress and die by atresia (subordinate follicles). The number of remaining (dominant) follicles is specific to the species and is indicative of litter size. Follicle waves develop during both luteal and follicular phases and it is the dominant follicle(s) of the last follicular wave that ovulates. However, there are cases where dominant follicles from the last two follicle waves can ovulate (sheep and goats). There are exceptions to the organized wave‐like pattern of follicle growth where follicle development is apparently continuous (pigs and chickens). In these animals many follicles develop to intermediate diameters and at specific times follicles that are destined to ovulate are selected from this pool and continue growing to ovulation. Understanding the pattern of follicle development in different species is increasingly important for designing improved methods to manipulate reproduction in domestic animals.  相似文献   

17.
Two groups of mouse preantral follicles with diameters of 125-150 and 151-175 microm were cultured individually for 6 days in a medium supplemented with FSH and fetal calf serum to determine their in vitro growth characteristics. Their oocyte capacity for maturation and development to the blastocyst stage following in vitro fertilization was also assessed. Antral formation rate at the end of culture was higher in the follicles of 151-175 microm (89%) than 125-150 microm (76%). The timing of antrum formation was different between the two follicle categories: most 151-175 microm follicles formed antra earlier than 125-150 microm follicles (days 4 and 5 vs. 5 and 6). However, follicle diameters at the time of antrum formation were the same regardless of the initial size and the culture period. Maturation rates of the oocytes derived from both categories of in vitro grown follicles (70 and 62%) were not different from those of oocytes from in vivo grown follicles (74%). The in vitro derived oocytes, however, showed less cleavage (30 and 35%) than the in vivo derived oocytes (89%). Although the oocytes from both follicle categories developed to the morula stage after in vitro fertilization, blastocysts were only obtained from oocytes derived from the 151-175 microm category. These results demonstrate that an individual follicle culture system using a medium with FSH and fetal calf serum supports in vitro growth of mouse preantral follicles with diameters of 151-175 microm to the preovulatory stage, and that their oocytes have the capability to develop to the blastocyst stage.  相似文献   

18.
To improve the reproductive performance of water buffalo to level can satisfy our needs, the mechanisms controlling ovarian follicular growth and development should be thoroughly investigated. Therefore, in this study, the expressions of growth differentiation factor‐9 (GDF‐9) in buffalo ovaries were examined by immunohistochemistry, and the effects of GDF‐9 treatment on follicle progression were investigated using a buffalo ovary organ culture system. Frozen–thawed buffalo ovarian follicles within slices of ovarian cortical tissue were cultured for 14 days in the presence or absence of GDF‐9. After culture, ovarian slices were fixed, sectioned and stained. The follicles were morphologically analysed and counted. Expression pattern of GDF‐9 was detected in oocytes from primordial follicles onwards, besides, also presented in granulosa cells. Moreover, GDF‐9 was detected in mural granulosa cells and theca cells of pre‐antral follicles. In antral follicles, cumulus cells and theca cells displayed positive expression of GDF‐9. In corpora lutea, GDF‐9 was expressed in both granulosa and theca lutein cells. After in vitro culture, there was no difference in the number of primordial follicles between cultured plus GDF‐9 and cultured control that indicated the GDF‐9 treatment has no effect on the primordial to primary follicle transition. GDF‐9 treatment caused a significant decrease in the number of primary and secondary follicles compared with controls accompanied with a significant increase in pre‐antral and antral follicles. These results suggest that a larger number of primary and secondary follicles were stimulated to progress to later developmental stages when treated with GDF‐9. Vitrification/warming of buffalo ovarian tissue had a little remarkable effect, in contrast to culturing for 14 days, on the expression of GDF‐9. In conclusion, treatment with GDF‐9 was found to promote progression of primary follicle that could provide an alternative approach to stimulate early follicle development and to improve therapies for the most common infertility problem in buffaloes (ovarian inactivity).  相似文献   

19.
During an oestrous cycle, a cohort of antral follicles develops into – depending on the species – one or more ovulatory follicles. The bovine oestrous cycle is characterized by two to three such cohorts or growth waves, only the last of which will result in an ovulation. In every growth wave, several antral follicles are recruited for development. Recruited follicles are subjected to a selection process, whereby ever decreasing levels of follicle stimulating hormone (FSH) are available to the FSH dependent follicles. In the cow, a single follicle from the cohort will acquire dominance. The ability of the dominant follicle to prosper under basic FSH levels is ascribed to a transition in hormone dependency from FSH to luteinizing hormone. The exact follicle selection mechanism remains, however, to be elucidated. The beginning of this article focuses on the recruitment, selection and dominance phases in antral follicle development. Subsequently, the conditions leading to successful maturation and ovulation are discussed. The next section expounds upon the mechanisms for exogenous modulation of follicular dynamics with the aim of superovulation/superstimulation, and finally prospective future research directions are sketched.  相似文献   

20.
毛囊是毛纤维的生长基础,决定毛纤维的性状,角蛋白是毛囊组成的重要成分之一。近年来,对毛囊生长发育和角蛋白基因的挖掘等取得了一定的进展。文章回顾了绵羊角蛋白基因的发现,已经与人类角蛋白基因相当,但在数量和分类上存在差异;笔者介绍了绵羊毛囊的形态学结构,简述了毛囊角蛋白基因的表达定位和影响毛纤维性状的角蛋白,并分析了毛囊中的蛋白质组学技术的应用对毛囊生长发育和毛纤维性状的重要作用,以期为绵羊毛囊生长发育和羊毛性状的分子选育提供新的研究思路。  相似文献   

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