• 제목/요약/키워드: spermatogenic ability

검색결과 5건 처리시간 0.018초

Involvement of lncRNA-HOTTIP in the Repair of Ultraviolet Light-Induced DNA Damage in Spermatogenic Cells

  • Liang, Meng;Hu, Ke
    • Molecules and Cells
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    • 제42권11호
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    • pp.794-803
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    • 2019
  • Ultraviolet light (UV)-induced cellular response has been studied by numerous investigators for many years. Long noncoding RNAs (lncRNAs) are emerging as new regulators of diverse cellular process; however, little is known about the role of lncRNAs in the cellular response to UV treatment. Here, we demonstrate that levels of lncRNA-HOTTIP significantly increases after UV stimulation and regulates the UV-mediated cellular response to UV through the coordinate activation of its neighboring gene Hoxa13 in GC-1 cells (spermatogonia germ cell line). UV-induced, G2/M-phase arrest and early apoptosis can be regulated by lncRNA-HOTTIP and Hoxa13. Furthermore, lncRNA-HOTTIP can up-regulate ${\gamma}-H_2AX$ and p53 expression via Hoxa13 in UV-irradiated GC-1 cells. In addition, p53 has the ability to regulate the expression of both lncRNA-HOTTIP and Hoxa13 in vitro and in vivo. Our results provide new data regarding the role lncRNAs play in the UV response in spermatogenic cells.

농도별(濃度別) 구자(?子) 투약(投藥)이 수컷 생쥐의 생식능력(生殖能力)에 미치는 영향(影響) (Effects of Allii tuberosi Semen Extract Solution on Reproductive Capacities in Mice)

  • 이창훈;조정훈;장준복;이경섭;김인중
    • 대한한방부인과학회지
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    • 제19권3호
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    • pp.41-54
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    • 2006
  • Purpose : These studies were undertaken to evaluate the effects of Allii tuberosi Semen (ATS) on the spermatogenic abilities such as concentration, motility and morphological normality of sperm from the testis and the activities of sperm hyaluronidase, testicular peroxidase and testicular catalase. Materials and Methods : We used the 8-week-old mice and administered the 0.2 ml extract solution of ATS in the different concentration (0.1 mg/ml, 1 mg/ml, 10 mg/ml and 100 mg/ml) once a day for 60 days. The control group was administered the distilled water in the same way. After the administration of each extract solution, we examined the number of total, motile and normal sperm, the activities of sperm hyaluronidase, testicular peroxidase and testicular catalase. Also we observed the histological changes of isolated testis. And we compared to the testicular tissue especially seminiferous tubules between control and treated group by histochemical methods. Results : The concentration of total sperm, the motility and normality of spermatozoa were significantly increased in ATS groups, especially in 1 and 10 mg/ml groups, compared to control group. In the histological analysis of the testicular tissues, the enlargement of testicular lobe diameter and apparent vasculogenesis between testicular lobes were observed in the ATS groups compared to the control group, respectively. Also, the activity of hyaluronidase was significantly increased in the ATS groups compared to the control group. In the antioxidant activity analysis, the activity of testicular peroxidase was significantly increased in the ATS groups compared to the control group, especially in 1 mg/ ml group. The activity of testicular catalase was increased in ATS groups. Conclusion : This study shows that ATS has the beneficial effect on the concentration, morphology and motility of sperm, the activities of sperm hyaluronidase and testicular peroxidase. We can suggest that ATS extract solution be useful for the treatment of male sexual dysfunctions and infertility.

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아연 전처리가 시간 경과에 따른 카드뮴 유도 고환 독성에 미치는 보호 효과 (Preventive Effects of Zinc Pretreatment in the Time-course of Cadmium-induced Testicular Toxicity in the Rat)

  • 제갈승주;이경선;정옥봉;임효빈
    • 대한임상검사과학회지
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    • 제41권3호
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    • pp.111-122
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    • 2009
  • Cadmium (Cd) is known to exert gonadotoxic and spermiotoxic effects. The present study was performed to investigate the morphological effects and metallothionein (MT) expression by zinc pretreatment in the course of time of cadmium-induced testicular injury in rat. Fifty male Spraque-Dawley rats weighing 160~180 g were divided into two groups : saline-pretreated cadmium group and zinc-pretreated cadmium group. Rats of two groups received subcutaneous injection of saline and 100 mg/kg $ZnSO_4$ at 0, 2, 5 and 8 hrs intervals respectively. Cadmium chloride (4.5 mg/kg $CdCl_2$) was administrated intraperitoneally at 2 hrs after zinc injection and rats were killed 0, 12, 24, 48 and 72 hrs later. Testicular tissue damages, interstitial (Leydig) cells status and MT expression were determined using hematoxylin-eosin stained sections and a computerized image analysis system on sections immunostained with a mouse anti-metallothionein respectively. Zinc pretreatment was significantly reduced testicular damages in five pathological categories after cadmium administation. The number of surviving interstitial cells was significantly higher in the zinc-pretreated group than in the saline-preatreated group at 48 and 72 hrs after cadmium administration. Non-damaged testis showed the positivity of MT staining in spermatogenic cells, Sertoli cells and endothelium of blood vessel, but not in the Leydig cells. The positivity of MT staining in saline-pretreated group was significantly reduced at 24 hrs after cadmium administration, whereas zinc-pretreated group showed strong MT positive staining similar to the 0 hr by 42 hrs after cadmium administration. In damaged testis, MT positive staining was also observed in the Leydig cells of both groups. These results suggest that a major preventive effect of zinc against cadmium-induced testicular toxicity may be due to its ability to reduce the cytotoxicity of cadmium in spermatogenic cells and Leydig cells by inhibiting the susceptibility of the testis to cadmium but not MT production by cadmium.

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아연 전처리가 시간 경과에 따른 카드뮴 유도 고환 독성에 미치는 보호 효과 (Preventive Effects of Zinc Pretreatment in the Time-course of Cadmium-induced Testicular Toxicity in the Rat)

  • 제갈승주;이경선;정옥봉;임효빈
    • 대한임상검사과학회지
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    • 제42권3호
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    • pp.136-148
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    • 2010
  • Cadmium (Cd) is known to exert gonadotoxic and spermiotoxic effects. The present study was performed to investigate the morphological effects and metallothionein (MT) expression by zinc pretreatment in the course of time of cadmium-induced testicular injury in rat. Fifty male Spraque-Dawley rats weighing 160-180 g were divided into two groups: saline-pretreated cadmium group and zinc-pretreated cadmium group. Rats of two groups received subcutaneous injection of saline and 100 mg/kg $ZnSO_4$ at 0, 2, 5 and 8 hrs intervals respectively. Cadmium chloride (4.5 mg/kg $CdCl_2$) was administrated intraperitoneally at 2 hr after zinc injection and rats were killed 0, 12, 24, 48 and 72 hrs later. Testicular tissue damages, Interstitial (Leydig) cells status and MT expression were determined using hematoxylin-eosin stained sections and a computerized image analysis system on sections immunostained with a mouse anti-metallothionein respectively. Zinc pretreatment was significantly reduced testicular damages in five pathological categories after cadmium administation. The number of surviving interstitial cells was significantly higher in the zinc-pretreated group than in the saline-preatreated group at 48 and 72 hrs after cadmium administration. Non-damaged testis showed the positivity of MT staining in spermatogenic cells, Sertoli cells and endothelium of blood vessel, but not in the Leydig cells. The potitivity of MT staining in saline-pretreated group was significantly reduced at 24 hrs after cadmium administration, whereas zinc-pretreated group showed strong MT positive staining similar to the 0 hr by 42 hrs after cadmium administration. In damaged testis, MT positive staining was also observed in the Leydig cells of both groups. These results suggest a major preventive effect of zinc against cadmium-induced testiculat toxicity may be due to its ability to reduce the cytotoxicity of cadmium in spermatogenic cells and Leydig cells by inhibiting the susceptibility of the testis to cadmium but not MT production by cadmium.

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EGFP 유전자가 도입된 반수체 정자세포에 의한 형질전환 설치류 난자의 생산 (Production of Transgenic Murine Embryos using Haploid Spermatids Transfected with EGFP Gene)

  • 강기예;송상진;이훈택;정길생
    • 한국가축번식학회지
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    • 제25권4호
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    • pp.305-315
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    • 2001
  • 본 연구의 목적은 외래 EGFP 유전자를 분화이전의 웅성생식세포에 도입한 후 이를 난모세포내에 미세주입하여 형질전환동물을 생산하는 기술을 개발하는 데에 있다. 이를 위하여 반수체 정자세포에서 특이적으로 발현하는 생쥐의 mTP1과 햄스터의 hPrm2 유전자 발현 시기를 RT-PCR로 조사한 결과 그시기는 생쥐와 햄스터에서 각각 18일령과 20일령으로 확인되었다. 이에 따라 외래 유전자의 침입이 용이한 감수분열 직전단계인 17일령의 생쥐와 19일령의 햄스터 정자세포를 EGFP 유전자가 포함된 배양액에 부유시킨 다음, 전기자극을 부여한 결과 0.18 ㎸/cm의 전기자극을 가한 후 72시간 배양한 정자세포의 28.5%와 32.1%에서 EGFP 유전자가 발현되는 것으로 확인되었다. EGFP유전자가 도입된 반수체 정자의 수정 및 발달 능력을 검증하기 위하여, 이들 정자세포를 햄스터 난자 내에 미세주입 하였으나, 형광현미경하에서는 EGFP유전자의 발현은 관찰할 수 없었다. 이에 이들 난자를 공시하여 PCR분석을 실시한 결과, 약 44%의 수정란에서 EGFP 유전자의 존재가 확인되었다. 이러한 결과로 보아 반수체 정자세포는 외래 유전자를 난자 내에 도입하기 위한 운반체로 이용될 수 있을 것으로 생각된다.

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