• 제목/요약/키워드: spermatogenic cells

검색결과 76건 처리시간 0.027초

Expression of Stage-Specific Genes on the Cultured Spermatogenic Cells Obtained from Prepubertal Porcine Testis

  • Song, Sang-Jin;Kim, Jung-Ho;Min, Dong-Mi;Park, Yong-Seog;Koong, Mi-Kyung;Seo, Ju-Tae;Lee, Hoon-Taek;Chung, Kil-Saeng
    • 한국동물번식학회:학술대회논문집
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    • 한국동물번식학회 2002년도 춘계학술발표대회 발표논문초록집
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    • pp.97-97
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    • 2002
  • Achieving of in vitro development for mammalian premature spermatogenic cells are very difficult. In-vitro culture of spermatogenic cells were then initiated in an effort to try to study in vivo spermatogenesis and to understand its molecular events. Recently, the morphogenetic changes of spermatocytes or spermatid by in-vitro culture system were achieved. (omitted)

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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.

개불(Urechis unicinctus) Sperm Ball과 정자의 미세구조와 금 입자 면역 반응에 의한 $\alpha-Tubulin$의 분포 (The Fine Structure of the Sperm Ball and Sperm of Urechis unicinctus and Immunogold Localization of $\alpha-Tubulin$)

  • 신길상
    • Applied Microscopy
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    • 제28권2호
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    • pp.193-205
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    • 1998
  • The Urechis unicinctus sperm and spermatogenic cells prepared from the testis are investigated to identify $\alpha-tubulin$ of axoneme microtubules using mouse monoclonal $anti-\alpha-tubulin$ as the first Ab and Gold(10nm) conjugated goat anti-mouse IgG as the Ab marker. The Ag-Ab reaction analyzed excellently the localization of $\alpha-tubulin$ and the gold particles incorporated with the proximal and distal centrioles, manchette microtubules, and flagellum. The gold particles can be also observed in the spermatogenic cells while the cells are still in sperm ball which is composed of a somatic cell and spermatogenic cells. The sperm ball is the functional unit of sperm production in U unicinctus testis. The spermatids are developed from the spermatogenic cells in the sperm ball and released into the testis cavity through a cortical cytoplasmic opening. The spermatid architectures are similar with the mature sperm of the testis cavity in aspects of shape of discoid acrosome, degree of nuclear condensation and ring type of mitochondrion. However, the distal centriole connecting with the flagella can be observed from the mature sperm while the both proximal and distal centrioles reveal only in the spermatids. The proximal centriole is directly connected with nuclear outer membrane during the stage of nuclear condensation and oriented perpendicularly to the distal centriole whose axis coinciding with the longitudinal axis of the spermatozoon. There are indications that the distal centriole is intimately associated with the polymerization of the flagellum. The manchette microtubules appear during spermatid development but the mature sperm have round head and no conspicuous middle piece.

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생쥐 정자세포의 분리와 체외 배양에 관한 연구 (In Vitro Culture Following Purfication of Mouse Spermatogenic Cells)

  • 김묘경;김진회;이상민;정/하해숙;이훈택;정길생
    • 한국가축번식학회지
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    • 제20권1호
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    • pp.43-52
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    • 1996
  • 본 연구는 생쥐의 고게정관내에 존재하는 분화단계의 정자세포를 발생단계별로 분리하여, 체외에서 단기간 배양체계를 확립하기 위하여 실시하였다. 8주령 이상된 생쥐의 정소로부터 정소막을 제거시킨 후, collagenase (1mg/ml), trypsin(2.5mg/ml)를 처리하여 곡세정관을 간질세포와 분리하여 배양액에 부유시켰다. 부유세포는 Celcep장치를 이용하여 세포크기와 밀도 차이에 의해 분화 단계별로 분리하였다. 회수된 세포의 균질성은 haematoxylin/eosin 또는 orcein으로 염색한 후, 광학현미경하에서 확인한 결과 약 85% pachytene spermatocyte와 round spermatid을 성공적으로 분리해냈다. 따라서 sedimentation velocity에 의해서 생쥐의 spermatogenic cell의 발달단계별 분리가 가능함을 알 수 있었다. 이러한 방법으로 분리된 pachytene spermatogenic cell들은 DMEM 배양액에서 6일 이상 배양한 결과 약 36%의 생존율을 보였다. 따라서, 분화단계별 정자 세포의 분리 및 배양체계의 확립은 웅성생식세포의 발생과정에 따른 생리 또는 분자생물학적 현상을 규명함은 물론 세포융합기술의 이용에 의한 형질전환동물 생산에의 응용을 통해 가축에 있어서의 형질전환 생산효율의 개선에 기여할 수 있으리라 사료된다.

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항-액틴-금 입자 표지에 의한 개불(Urechis unicinctus) 정자 및 정세포 핵 Actin의 분포 (Localization of Anti-Actin-Gold Particles (10 nm) Labeled to Nuclear Actin of Urechis Sperm and Spermatids)

  • 신길상;김호진;김완종
    • Applied Microscopy
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    • 제30권4호
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    • pp.403-412
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    • 2000
  • 1. 아메바 항-액틴의 Ag-Ab 반응과 이를 항-생쥐 IgG-금 입자로 표지한 결과는 주로 정세 포 및 정자의 핵질에 특이적으로 표지되었고 첨체에서는 그 반응을 볼 수 없었다. 2. 표지된 항-액탠 금 입자로 볼 때 정자 핵질의 G-액틴 또는 G-actin oligomer는 정세포의 F-액틴에서 유래되는 것으로 사료된다. 3. 첨체의 액틴은 주로 F-액틴으로 첨체돌기 형성에 참여하지 않는 위상인 것으로 관찰된다. 4. 미세구조의 변화, 정세포 체적의 감소, 정세포 및 정자 핵에 표지되는 금 입자의 증가와 이들 현상이 나타나는 동시성으로 볼 때 정세포 핵의 형태변화의 내용은 응축이고 이는 F-actin의 탈중합 반응에 의한 G-액틴의 생성이 원인일 것으로 사료된다.

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Histological Features of the Testis in the Long-beaked Common Dolphin from Korean Waters

  • Kim, Juhwan;Jang, Sungwoong;Jeon, Yubyeol;An, Du Hae;Kim, Doo Nam;Hyun, Sang-Hwan;Moon, Changjong
    • 한국수정란이식학회지
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    • 제28권1호
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    • pp.73-78
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    • 2013
  • The present study examined the histological characteristics of adult testis in the long-beaked common dolphin (Delphinus capensis) from Korean waters and the localization of DEAD-box polypeptide 4 (DDX4; a germ cell marker) and vimentin (a Sertoli cell marker) expression in the dolphin testis compared with that in terrestrial mammals, including dogs and rats. The seminiferous tubules of dolphin testis have very small or completely closed lumens, and spermatogenic cells and Sertoli cells within the tubules cannot be differentiated. Immunohistochemical analysis showed that, in the dolphin testis, DDX4- and vimentin-positive cells were scattered extensively within the tubule, whereas in the dog and rat testis, DDX4 immunoreactivity was localized in spermatogenic cells of the adluminal compartment, and vimentin immunoreactivity was localized in Sertoli cells of the basal compartment in the seminiferous epithelium. These results suggest that the histological characteristics of the seminiferous tubules in the dolphin testis differ from those of terrestrial species.

Developmental Phases of the Seminal Vesicle related to the Spermatogenic Stages in the Testicular Lobules of Neptunea (Barbitonia) cumingii (Gastropoda: Buccinidae)

  • Kim, Sung Han
    • 한국발생생물학회지:발생과생식
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    • 제20권3호
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    • pp.247-254
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    • 2016
  • Cytological changes of the epithelial cells according to the developmenatal phases of the seminal vesicle related to the spermatogenic stages in the testicular lobules during spermagenesis in male Neptunea (Barbitonia) cumingii (Gastropoda: Buccinidae) were investigated monthly by electron microscopical and histological observations. N. (B) cumingii is dioecious, and an internal fertilization species. The male genital organ is located near the tentacles. The spermatozoon is approximatley $50{\mu}m$ in length. The axoneme of the tail flagellum consists of nine pairs of microtubles at the periphery and one pair at the center. The process of germ cell development during spermatogenesis can be divided into five succesive stages: (1) spermatogonia, (2) primary spermatocytes, (3) secondary spermatocytes, (4) spermatids, and (5) spermatozoa. A considerable amount of spermatozoa make their appearance in the testicular lobules (or acini) and some of them are tranported from the testis towards the seminal vesicles until late July. In this study, the developmental phases of the epithelial cells of the seminal vesicles of N. (B.) cumingii could be classified into four phases: (1) S-I phase (resting), (2) S-IIphase (early accumulating), (3) S-III phase (accumulating), and (4) S-IV phase (spent). However, in case of N. (B.) arthritica cumingii, the developmental phases of the seminal vesicle were devided into three phases: (1) resting, (2) accumulating and (3) spent. Granular bodies in the inner layer of the seminal vesicles are involved in resorption of digestion of residual spermatozoa.

한국산 꿩 곡세정관내 정자형성세포의 형태학적 분류 (The Morphological Classification of the Spermatogenic Cells in the Seminiferous Tubule of the Korean Native Pheasant(Phasianus colchicus korpowi))

  • 박영석;양홍현
    • 한국가축번식학회지
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    • 제23권1호
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    • pp.45-51
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    • 1999
  • 본 연구는 성성숙한 번식기의 한국산 숫컷 꿩을 대상으로 번식연구의 기초자료를 얻기 위해 곡세정관의 정자형성세포를 분류하였다. 그 결과는 다음과 같다. 1. 정조세포는 A형, In형 및 B형의 3 가지 정조세포로 분류되었다. 2. 제 Ⅰ정모세포는 전세사기, 세사기, 접합기, 태사기 및 이동기의 5가지 형 제 1 정모세포로 분류되었다. 3. 정자세포는 핵의 변화에 따라서 둥근 정자세포에서 장축성장한 정자세포로 성장하는 과정을 7 단계로 분류되었다.

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韓國産 冬眠 박쥐의 精巢와 副精巢의 週期的인 變化에 관한 硏究 (Periodic Changes of the Testis and Ductus Epididymis in Korean Hibernating Bats)

  • Oh, Yung-Keun
    • 한국동물학회지
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    • 제20권2호
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    • pp.67-76
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    • 1977
  • The periodic changes of testis and \ulcorner션 epididymidis in Korean hibernating bats, the oriental discoloured bats (Vesportilio superans Thomas) and the Korean greater horseshoe bats (Rhinolophus ferrumequinum korak Kuroda) were studied in order to clarify the possibility of correlation between their histological findings and one of physiological facets, hibernation, and the results obtained were as follows: 1. The spermatogenic function of the oriental discoloured bats obtained in July and August was depressed although the spermatocytes showed a considerable cell proliferation. Few mature sperms were observed in the seminiferous tubules of the bat obtained in August. 2. The spermatogenic function of the Korean greater horeshoe bats obtained in September was not remalkable but a considerable number of sperms were stored in the excretory ducts which were characterized by existence of para-tubular spaces in the ductus epididymidis. 3. The spermatogenic epithelia of the Korean greater horseshoe bats obtained in December showed histologically atrophied figures. However, a vast number of sperm remained in extremely expaned luminae of the ductuc epididymidis which epithelial cells were maintained rectangular in shape. 4. These results suggest that there are periodic changes of the spermatogenic epithelia and the excretory ducts, and that those histological changes are closely related to their wintering.

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수컷랫드에 있어서 새로운 안트라사이클린계 항암제 DA-125의 생식독성 연구 (Male Reproductive Toxicity of DA-125, a New Anthracycline Anticancer Agent, in Rats)

  • 김종춘;김갑호;신호철;정문구
    • Toxicological Research
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    • 제14권2호
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    • pp.193-203
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    • 1998
  • The toxicity of DA-125. a new anthracycline anticancer agent, on the male reproductive system was studied in Sprague-Dawley rats. Forty male rats were rando$m\ell$y assigned to Jour groups with ten rats in each group and given single intraveneous doses of DA-125 at dose levels of 0. 12.5. 25. and 50 mg/kg body weight. On day 56 after treatment the animals were allowed to mate. and their male reproductive Junctions and organs were examined in detail. Copulated females were sacrificed on day 20 of gestation for examination of embryo-fetal development. One out of ten rats in the 50 mg/kg group died on day 12 after treatment. Clinical signs such as emaciation. sedation, anorexia. swelling. dark material around eye. alopecia. and diarrhea were observed in the 25 and/or 50 mg/kg groups. Reduction in the body weight gain. decrease in the absolute weights of testes. epididymis and seminal vesicles. and/or decrease in the number of testicular sperm heads were also found. Although histopathological changes such as atrophy of seminiferous tubules. loss or decrease of spermatogenic cells. exfoliation of spermatogenic cells. vacuolization of Sertoli cells. decrease of sperm. and/or increase of necrotic spermatogenic cells in epididymal ducts were observed. no adverse effects on the motility and morphology of epididymal sperm. copulation index. fertility index. and embryo-fetal development were detected in the 25 and 50 mg/kg groups. There were no evidences of male reproductive toxicity in the 12.5 mg/kg group. These results show that single intravenouse doses of DA-125 produce significant dose-related testicular atrophy. histopathological changes. and oligozoospermia in rats and $LD_{10}$ for DA-125 appears to be 50 mg/kg body weight.

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