• Asian-Australasian Journal of Animal Sciences
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• 제4권3호
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• pp.251-254
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• 1991

Immobilized (killed) mouse spermatozoa or sperm head were microinjected into mouse oocytes matured in vivo and cultured for 72h in vitro. When non-capacitated spermatozoon was injected, oocytes that developed to $${\geq_-}$$ 2-cell and $${\geq_-}$$ 4-cell was 27.8 (15/54) and 3.7% (2/54), respectively. When non-capacitated sperm head was injected. development to $${\geq_-}$$ 2-cell and $${\geq_-}$$ 4-cell was 21.3 (16/75) and 8.0% (6/75), respectively. When capacitated spermatozoon was injected, development to $${\geq_-}$$ 2-cell and $${\geq_-}$$ 4-cell was 21.4 (15/70) and 4.3% (3/70), respectively. When capacitated sperm head was injected, development to $${\geq_-}$$ 2-cell and $${\geq_-}$$ 4-cell was 29.9 (35/117) and 10.3% (12/117), respectively. In contrast, none developed beyond 4-cell in the sham-operated group. The results of this study demonstrated that mouse oocytes matured in vivo can undergo normal appearing cleavage to 4-cell stage by dead-sperm injection. Sperm treatment prior to injection did not affect the ability of mouse oocytes to cleave in vitro.

• 한국동물번식학회:학술대회논문집
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• 한국동물번식학회 2001년도 춘계학술발표대회
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• pp.12-12
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• 2001

To get insight into the nature of foreign mitochondria and syngamy during mammalian fertilization we compared fertilization processes in porcine oocytes following microinjection of porcine or mouse spermatozoa. Pronuclear movement, sperm mitochondria, and DNA synthesis were imaged with propidium iodide, mitotracker, and BrdU under confocal laser scanning microscope. Intracytoplasmic injection of either porcine or mouse spermatzoon activated porcine oocytes without additional parthengenetic stimulation. Foreign mitochondria in either mouse or porcine sperm midpiece were introduced into porcine oocytes following sperm injection, but rapidly disappeared from the actively developing porcine oocytes. BrdU experiment showed new DNA synthesis in porcine oocytes following injection of mouse spermatozoon or sperm head. At 24 h after injection of mouse isolated sperm head or a spermatozoon, mitoic metaphase was seen in oocyte, but they did not go to normal cell division (Table). These results suggest that pronuclear formation, foreign mitochondria disruption, DNA synthesis and syngamy formation during fertilization are not species specific processes.(Table Omitted).

• 농업과학연구
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• 제49권3호
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• pp.451-462
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• 2022

Dioscorea bulbifera tubers contain several phytochemicals of pharmaceutical value. They have been traditionally used for treating various ailments, including postmenopausal symptoms. In the present study, we analyzed the direct effects of Dioscorea tuber extract on mouse spermatozoa. Its contraceptive effect was also evaluated by an intravaginal application before copulation. Mouse spermatozoa were cultured in vitro with various concentrations of the extract. After culturing, the spermatozoa were stained with fluorescein isothiocyanate peanut agglutinin or Coomassie blue to study the acrosome reaction, stained with trypan blue to study the viability, or treated with a hypo-osmotic medium to study the membrane damage. Estrous female mice were intravaginally injected with the extract and copulated with males. The extract induced acrosome exocytosis, viability loss, and membrane damage in a concentration-dependent manner. Female mice treated with the extract showed complete loss of fertility. These observations indicate that the Dioscorea bulbifera tuber extract could be used as a topical contraceptive. Infertility could be due to the precocious acrosome exocytosis of the spermatozoa or membrane damage.

• 한국동물학회지
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• 제32권3호
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• pp.264-274
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• 1989

본 실험은 생쥐에서 부정소액내의 단백질 성분과 조성에 미치는 정소액과 정자의 영향을 알아보기 위하여, 성적 성숙시기에 따라 정소와 부정소의 조직분화 양상을 관찰하였으며, 강소분화 특징에 따라 체취한 부정소액은 전기영동법으로 단백질을 분석하여 다음과 같은 결과를 얻었다. 정소와 부정소는 생후 10일군에서 미분화 상태였고, 20일군에서 세정관의 강소는 형성되지 않았으나 부정소는 두부에서 미부에까지 강소가 형성되었으며, 35일군에서는 정소내 세정관의 강소가 형성되었고 정세포는 정자로 분화되었고, 부정소의 상피세포는 principal cell과 clear cell로 분화되었으나 부정소로 유입된 정자는 없었다. 80일군에서는 정소와 부정소가 완전히 본화되었고 부정소로 유입된 많은정자가 관찰되었다. 그리고 부정소액의 전기영동상에는 혈청내의 성분과 다른 단백질이 모두 28종이 나타났는데, 그 중 12종은 부정소액에만 존재하는 부정소 특이단백질이었고, 16종은 정소액에도 공통으로 존재하는 단백질이었다. 또한 이 단백질들은 성숙시기에 따라 종류가 다르게 나타났으며, 성체에서 나타난 3종의 단백질은 부정소의 부위에 따라 양적인 변화를 나타냈다. 이상의 결과로 보아 부정소액내 단백질의 성분과 조성은 정자를 포함한 정소액의 유입과 부정소 상피세포의 분비 및 흡수의 조절작용에 의하여 변화되는 것으로 사료된다. 따라서 부정소액내의 TEP와 ESP는 부정소 정자의 성숙에 어떤 중요한 역할을 할 것으로 사료된다.

• 한국동물학회:학술대회논문집
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• 한국동물학회 1996년도 공동 춘계학술대회
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• pp.49.2-49
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• 1996

No Abstract, See Full Text

• BMB Reports
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• 제41권9호
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• pp.664-669
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• 2008

Znf230, the mouse homologue of the human spermatogenesis-related gene, ZNF230, has been cloned by rapid amplification of cDNA ends (RACE). This gene is expressed predominantly in testis, but its expression in different testicular cells and spermatogenic stages has not been previously analyzed in detail. In the present study, the cellular localization of the Znf230 protein in mouse testis and epididymal spermatozoa was determined by RT-PCR, immunoblotting, immunohistochemistry and immunofluorescence. It is primarily expressed in the nuclei of spermatogonia and subsequently in the acrosome system and the entire tail of developing spermatids and spermatozoa. The results indicate that Znf230 may play an important role in mouse spermatogenesis, including spermatogenic cell proliferation and sperm maturation, as well as motility and fertilization.

• 한국발생생물학회지:발생과생식
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• 제3권1호
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• pp.87-93
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• 1999

생쥐 정자의 수정능력획득과 첨체반응에 작용하는 $Na^{+}$/H$^{+}$ antiporter의 역할을 조사하고자 하였다. $Na^{+}$/H$^{+}$ antiporter를 특이적으로 억제하는 dimethyl amiloride는 정자의 자발적인 첨체반응을 농도 의존적으로 억제한 반면 난포액 및 calcium ionophore인 A23l87에 의해 유도된 첨체반응은 억제하지 못하였다. 이러한 결과는 정자내 $Na^{+}$/H$^{+}$ antiporter에 의한 1가이온의 출입과 이에 따른 세포질내 pH 조절이 정자의 수정능력 획득과 자발적인 첨체반응에 조절요인으로 작용함을 암시한다. 수정능력을 획득한 정자에서 난포액 등의 agonist 또는 A23l87에 의해 유도되는 첨체반응은 $Na^{+}$/H$^{+}$ antiporter와는 무관하게 진행되는 것으로 사료된다.

• Reproductive and Developmental Biology
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• 제36권3호
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• pp.225-230
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• 2012

Interferon induced transmembrane protein-1 (Ifitm-1) has been reported to have an important role in primordial germ cell formation, and it has expressed in female reproductive organ. In the present study, Ifitm-1 gene expression was identified in testes and all part of epididymis using western immunoblot and immunohistochemistry. Interestingly, Ifitm-1 expression was observed on the head of spermatozoa. To investigate the role of Ifitm-1 gene expression in behavior of spermatozoa after acrosome reaction, fresh sperm was incubated with calcium ionophore to induce acrosome reaction, whereas the expression of Ifitm-1 was not altered after the acrosome reaction. Then to identify the effect of Ifitm-1 in sperm motility and other seminal parameters, different concentration of Ifitm-1 antibody was incubated with spermatozoa, and seminal parameters were assessed using computer-assisted semen analysis (CASA). Interestingly, motility, progressive, and VAP were increased in the sperm with Ifitm-1 antibody treated compared to rabbit serum, however other parameters such as straightness were not changed. In order to identify the functional significance of Ifitm-1 in fertilization, capacitated spermatozoa were pre-incubated with anti-Ifitm-1 antibody and subsequently examined the ability to adhere to mouse oocytes. However, any defection or alteration in sperm-egg fusion was not found, Ifitm-1 antibody treated or non-treated spermatozoa showed a normal penetration. Although the precise role of Ifitm-1 in sperm motility and following fertilization need to be elucidated, this study suggests that the activation of Ifitm-1 on the sperm may enhance the motility of spermatozoa in mice.

• 한국수정란이식학회:학술대회논문집
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• 한국수정란이식학회 2006년도 The 6th Intermational Symposium on Developmental Biotechnology
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• pp.80-81
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• 2006

• 한국동물학회:학술대회논문집
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• 한국동물학회 1996년도 한국생물과학협회 국제학술대회
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• pp.150.1-150
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• 1996

No Abstract, See Full Text