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PLoS Gene:揭示成年雌性动物卵巢中存在前体生殖细胞 仍可分化为卵细胞 [复制链接]

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发表于 2012-8-13 16:53 |只看该作者 |倒序浏览 |打印
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2012年8月12日 讯 /生物谷BIOON/ --近日,一项针对来自胚胎期的未成熟卵子(卵母细胞)起源的研究为科学界一直以来的争议提供了新的信息,由于女性生物钟的原因,卵母细胞的数量随着其年龄的增加而逐渐减少,而且古代教条主义认为,哺乳动物在产后其卵母细胞并不能够自我更新。刊登在近日的国际杂志PLoS Genetics上的一篇研究报告中,来自麻省总医院和爱丁堡大学的研究者揭示了妇女在其成年生活中依然可以产生新的卵细胞。8 M) `- ?+ W- x# _5 U9 {* ]
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卵子是由处于有丝分裂周期的起源生殖细胞(或生殖祖细胞)所产生的,生殖祖细胞通过细胞分裂结束了其增值的能力,最终进入减数分裂期,单一的产生卵细胞和精子。传统观念认为雌性哺乳动物自出生以后就携带有毕生所有的卵细胞了,然而研究者的最新研究表明,成年鼠和人类的卵巢存在有罕见的生殖祖细胞(称为oogonial干细胞),其有能力分化并产生卵母细胞。
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. u6 `2 l4 ~6 r) q- T研究者使用了一种强大的遗传工具来追踪随着年龄增长的细胞的分裂过程和数量。如果传统的观念是正确的,所有的细胞分裂应该在出生之前都已经发生了,因此所有的卵细胞应该表现出相同的年龄深度。然而研究结果恰恰相反,随着雌性小鼠的生长,卵细胞的年龄明显增加了。
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0 d$ v0 H; X9 d2 j' l& I1 }. l尽管研究者的研究局限于小鼠之中,但是也提供了明显的证据揭示:oogonial干细胞同样存在于生育年龄的妇女卵巢中,而且这些干细胞拥有完全的能力,可以在实验条件下产生新的卵细胞。当然后期研究者还会进行深入研究来提供更多的证据。(生物谷Bioon.com)- F' G3 I* v; F( x9 \# O

5 d" j6 I% K, D, x, Z9 r% N% q, o编译自:Do ovaries continue to produce eggs during adulthood?2 y/ v: _7 O6 X. [! n8 U$ `+ B/ e
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发表于 2012-8-20 20:20 |只看该作者
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发表于 2012-8-21 16:25 |只看该作者
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发表于 2012-9-12 23:30 |只看该作者
Do ovaries continue to produce eggs during adulthood?
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Story Source
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: X% ]3 ~5 }' u% s9 ]A compelling new genetic study tracing the origins of immature egg cells, or 'oocytes', from the embryonic period throughout adulthood adds new information to a growing controversy. The notion of a "biological clock" in women arises from the fact that oocytes progressively decline in number as females get older, along with a decades-old dogmatic view that oocytes cannot be renewed in mammals after birth. After careful assessment of data from a recent study published in PLoS Genetics, scientists from Massachusetts General Hospital and the University of Edinburgh argue that the findings support formation of new eggs during adult life; a topic that has been historically controversial and has sparked considerable debate in recent years.
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Eggs are formed from progenitor germ cells that exit the mitotic cycle, thereby ending their ability to proliferate through cell division, and subsequently enter meiosis, a process unique to the formation of eggs and sperm which removes one half of the genetic material from each type of cell prior to fertilization.1 `+ z2 A5 T3 {. Y) ]0 M

( `( t# [6 Z7 x& S, m5 B7 |5 s2 ZWhile traditional thinking has held that female mammals are born with all of the eggs they will ever have, newer research has demonstrated that adult mouse and human ovaries contain a rare population of progenitor germ cells called oogonial stem cells capable of dividing and generating new oocytes. Using a powerful new genetic tool that traces the number of divisions a cell has undergone with age (its 'depth') Shapiro and colleagues counted the number of times progenitor germ cells divided before becoming oocytes; their study was published in PLoS Genetics in February this year.1 t) Q: H# @. v* r5 {- i( r9 y9 v

* ^( K( b6 u  G* M" ?8 k/ r+ SIf traditional thinking held true, all divisions would have occurred prior to birth, and thus all oocytes would exhibit the same depth regardless of age. However, the opposite was found – eggs showed a progressive increase in depth as the female mice grew older.+ v1 w* n' l3 ~. \

8 W8 T& r0 v" k: _/ c4 _; ]* eIn their assessment of the work by Shapiro and colleagues – published recently in a PLoS Genetics Perspective article – reproductive biologists Dori Woods, Evelyn Telfer and Jonathan Tilly conclude that the most plausible explanation for these findings is that progenitor germ cells in ovaries continue to divide throughout reproductive life, resulting in production of new oocytes with greater depth as animals age.; Z: R( {7 K0 H0 }- t

: H- Q& m* C/ d% _4 _; I) h6 d. P% v. eAlthough these investigations were performed in mice, there is emerging evidence that oogonial stem cells are also present in the ovaries of reproductive-age women, and these cells possess the capacity, like their mouse counterparts, to generate new oocytes under certain experimental conditions. While more work is needed to settle the debate over the significance of oocyte renewal in adult mammals, Woods and colleagues emphasize that "the recent work of Shapiro and colleagues is one of the first reports to offer experimental data consistent with a role for postnatal oocyte renewal in contributing to the reserve of ovarian follicles available for use in adult females as they age."
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