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老龄猪卵母细胞的细胞骨架改变与孤雌生殖

Cytoskeletal alteration in aged porcine oocytes and parthenogenesis.

作者信息

Kim N H, Moon S J, Prather R S, Day B N

机构信息

Department of Animal Sciences, University of Missouri-Columbia 65211, USA.

出版信息

Mol Reprod Dev. 1996 Apr;43(4):513-8. doi: 10.1002/(SICI)1098-2795(199604)43:4<513::AID-MRD14>3.0.CO;2-#.

Abstract

The objective of this study was to examine the changes in microtubule and microfilament assembly in aged porcine oocytes and to determine their developmental pattern after parthenogenetic activation. Porcine oocytes were cultured in Whitten's medium containing 10% follicular fluid with hormonal supplements (eCG and hCG) for 22 hr and 40 hr additional culture without hormonal supplements. At 40, 50, and 60 hr of culture, the oocytes were fixed for immunocytochemistry or activated by electrical pulse. In metaphase II stage oocytes, microtubules were detected only in the meiotic spindle. Two microfilament domains existed in the egg cortex, a thick and a thin microfilament domain. In aged oocytes (50 and 60 hr of culture), the incidence of metaphase II plates observed outside of the thick microfilament domain was higher (P < 0.05) than in young oocytes (40 hr of culture). After activation, a polar body was usually emitted from the chromatin at the microfilament rich domain or two pronuclei were formed outside of the microfilament rich domain. The percentage of activated oocytes with one female pronucleus was higher (P < 0.05) in oocytes at 40 hr of maturation than at 50 and 60 hr of culture. At 24 and 30 hr after stimulation the incidence of cleavage to the 3- to 4-cell stage was higher (P < 0.05) in aged oocytes (50 and 60 hr of maturation) than that in oocytes at 40 hr of culture. These results suggested that a role of microfilaments is to retain the chromatin at the proper position in the oocyte cortex, and that aging results in a disruption of the microfilaments such that atypical development results after parthenogenetic activation.

摘要

本研究的目的是检测老龄猪卵母细胞中微管和微丝组装的变化,并确定孤雌激活后它们的发育模式。将猪卵母细胞在含有10%卵泡液及激素补充剂(eCG和hCG)的惠滕氏培养基中培养22小时,然后在无激素补充剂的情况下再培养40小时。在培养40、50和60小时时,将卵母细胞固定用于免疫细胞化学或通过电脉冲激活。在中期II期卵母细胞中,仅在减数分裂纺锤体中检测到微管。卵母细胞皮质中存在两个微丝区域,一个厚微丝区域和一个薄微丝区域。在老龄卵母细胞(培养50和60小时)中,在厚微丝区域外观察到的中期II板发生率高于年轻卵母细胞(培养40小时)(P < 0.05)。激活后,通常在富含微丝的区域从染色质发出一个极体,或者在富含微丝的区域外形成两个原核。成熟40小时的卵母细胞中具有一个雌性原核的激活卵母细胞百分比高于培养50和60小时的卵母细胞(P < 0.05)。在刺激后24和30小时,老龄卵母细胞(成熟50和60小时)中分裂至3至4细胞期的发生率高于培养40小时的卵母细胞(P < 0.05)。这些结果表明,微丝的作用是将染色质保留在卵母细胞皮质的适当位置,并且衰老导致微丝破坏,从而在孤雌激活后导致非典型发育。

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