中山大学学报(医学科学版)
中山大學學報(醫學科學版)
중산대학학보(의학과학판)
JOURNAL OF SUN YAT-SEN UNIVERSITY(MEDICAL SCIENCES)
2008年
3期
241-247
,共7页
金黄地鼠%前列腺%子宫腔精子%膜蛋白
金黃地鼠%前列腺%子宮腔精子%膜蛋白
금황지서%전렬선%자궁강정자%막단백
golden hamster%ventral prostate%uterin sperm%protein
[目的]在整体水平探讨前列腺分泌蛋白对金黄地鼠精子膜蛋白的影响.[方法]雄性鼠手术分为4组,分别为附属性腺全去组,腹前列腺摘除组,去除其他附属性腺仅保留腹前列腺组和假手术组,每组动物6只.收集与保留前列腺及去除组的雄性鼠交配后的子宫腔精子,抽提精子膜蛋白,膜蛋白经聚丙烯酰胺凝胶(SDS-PAGE)和二维电泳凝胶分析,比较前列腺存在与否精子膜蛋白组分的异同.[结果]与不同组雄鼠交配后收集的子宫腔精子膜蛋白SDS-PAGE电泳谱主要条带类似.含腹前列腺组的精子膜组分中相对分子质量15 k、29 k、38 k、55 k和91 k多肽的量较去除腹前列腺组的子官腔精子膜相应组分增加.二维电泳结果示与含腹前列腺组雄鼠交配后收集的子宫腔精子膜蛋白较无腹前列腺组的精子膜蛋白多出10个蛋白斑点(MM/IP分别为16k/8.60、16.5k/9.2、28k/5.88/6.10、29k/5.98、32k/6.35/6.50/7.20、61k/5.90、83k/6.40),另外蛋白斑点量增加有11个.[结论]腹前列腺可修饰和调节精子膜蛋白,进而这些蛋白可能对雄性生殖力及胚胎的发育起作用.
[目的]在整體水平探討前列腺分泌蛋白對金黃地鼠精子膜蛋白的影響.[方法]雄性鼠手術分為4組,分彆為附屬性腺全去組,腹前列腺摘除組,去除其他附屬性腺僅保留腹前列腺組和假手術組,每組動物6隻.收集與保留前列腺及去除組的雄性鼠交配後的子宮腔精子,抽提精子膜蛋白,膜蛋白經聚丙烯酰胺凝膠(SDS-PAGE)和二維電泳凝膠分析,比較前列腺存在與否精子膜蛋白組分的異同.[結果]與不同組雄鼠交配後收集的子宮腔精子膜蛋白SDS-PAGE電泳譜主要條帶類似.含腹前列腺組的精子膜組分中相對分子質量15 k、29 k、38 k、55 k和91 k多肽的量較去除腹前列腺組的子官腔精子膜相應組分增加.二維電泳結果示與含腹前列腺組雄鼠交配後收集的子宮腔精子膜蛋白較無腹前列腺組的精子膜蛋白多齣10箇蛋白斑點(MM/IP分彆為16k/8.60、16.5k/9.2、28k/5.88/6.10、29k/5.98、32k/6.35/6.50/7.20、61k/5.90、83k/6.40),另外蛋白斑點量增加有11箇.[結論]腹前列腺可脩飾和調節精子膜蛋白,進而這些蛋白可能對雄性生殖力及胚胎的髮育起作用.
[목적]재정체수평탐토전렬선분비단백대금황지서정자막단백적영향.[방법]웅성서수술분위4조,분별위부속성선전거조,복전렬선적제조,거제기타부속성선부보류복전렬선조화가수술조,매조동물6지.수집여보류전렬선급거제조적웅성서교배후적자궁강정자,추제정자막단백,막단백경취병희선알응효(SDS-PAGE)화이유전영응효분석,비교전렬선존재여부정자막단백조분적이동.[결과]여불동조웅서교배후수집적자궁강정자막단백SDS-PAGE전영보주요조대유사.함복전렬선조적정자막조분중상대분자질량15 k、29 k、38 k、55 k화91 k다태적량교거제복전렬선조적자관강정자막상응조분증가.이유전영결과시여함복전렬선조웅서교배후수집적자궁강정자막단백교무복전렬선조적정자막단백다출10개단백반점(MM/IP분별위16k/8.60、16.5k/9.2、28k/5.88/6.10、29k/5.98、32k/6.35/6.50/7.20、61k/5.90、83k/6.40),령외단백반점량증가유11개.[결론]복전렬선가수식화조절정자막단백,진이저사단백가능대웅성생식력급배태적발육기작용.
[Objective] To investigate the effect of the secretory proteins of the ventral prostate glands on the sperm membrane proteins in golden hamsters. [Methods] The sperm was collected from female hamsters uteri after mated with the males with or without ventral prostate gland. Male golden hamsters were divided into four experimental groups: (i) all accessory sex glands (ASG) removed; (ii) ventral prostate gland removed; (iii) all ASG removed except ventral prostate gland and (iv) sham-operated controls. Each group contained 6 hamsters. The sperm membrane proteins were extracted from uterine sperm and analyzed by SDS-PAGE and two dimension electrophoresis. [Results] The SDS-PAGE results of sperm membrane showed that the ventral prostate glands added up some proteins or increased the quantity of some proteins, which contained molecular mass (MM)15 k, 29 k, 38 k, 55 k, and 91 k proteins, to the sperm membrane. 2D-electrophoresis of sperm membrane showed that some extra protein spots were appeared in with ventral prostate gland groups, their MM and isoelectric point (IP) corresponding to 16 k/8.60, 16.6 k/9.20, 28 k/5.88, 28 k/6.10, 29 k/5.98, 32 k/6.35, 32 k/6.50, 32 k/7.20, 61 k/5.90,and 83 k/6.40, respectively. The quantity of some protein spots increased in sperm membrane of ventral prostate glands group, their MM/IP coresponding to 17 k/5.95, 17.5 k/6.50, 24 k/7.20, 26 k/5.40, 26 k/5.60, 27 k/7.20, 27 k/7.50, 28 k/5.70, 29 k/8.50, 42 k/6.50, and 42 k/7.00, respectively. [Conclusion] The ventral prostate gland secretion plays a role in regulating the sperm membrane proteins and the latter may in turn affect the male fertility or embryo development.