• Title/Summary/Keyword: seminiferous tubule

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Morphological change of Sertoli cells in the pheasant(Phasianus colchicus) testis in active and inactive phase of spermatogenesis (꿩의 정자형성기와 비형성기의 정소내 Sertoli cell의 형태적변화)

  • Yang, Hong-hyun;Paik, Young-ki;Kim, In-shik
    • Korean Journal of Veterinary Research
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    • v.34 no.1
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    • pp.9-18
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    • 1994
  • The morphological changes of Sertoli cells of the Korean native pheasant were studied in the active and inactive spermatogenic phases. Twenty-four male of the pheasants were studied in the active (April~June) and inactive(August~March) phase. These data are useful in studying the male genital organs of the Korean native pheasant. Light microscopic morphological changes of the Sertoli cells were studied on paraffin-embedded sections stained with hematoxylin-eosin stain. Ultrastructural changes of Sertoli cells were investigated of ultrathin section using electron microscope. Results are summarized as follows: During the active phase, the average diameter of seminiferous tubule was $245.33{\pm}29.93{\mu}m$ and was largely decreased by $94.50{\pm}14.10{\mu}m$, and the thickness of interstitial tissue was comparatively increased during the inactive phase. During the active phase, in the cytoplasmic process of Sertoli cell and lipid droplets appeared disperse. Well-developed smooth Endoplasmic Reticulum and microtuble were observed in the cytoplasmic process. The nuclei of Sertoli cells were adjacent to the basement membrane. The size of nuclei was reduced and nuclei of Sertoli cells were densely packed within the tubule. Few collagen fibers, fibroblast and various sizes of lipid droplets were observed in the interstitial cell of the seminiferous tubule.

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Testicular Characteristics and the Block to Spermatogenesis in Mature Hinny

  • Han, Hongmei;Wang, Aihong;Liu, Liming;Zhao, Gaoping;Su, Jie;Wang, Biao;Li, Yunxia;Zhang, Jindun;Wu, Baojiang;Sun, Wei;Hu, Shuxiang;Li, Shuyu;Zhao, Lixia;Li, Xihe
    • Asian-Australasian Journal of Animal Sciences
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    • v.29 no.6
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    • pp.793-800
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    • 2016
  • Most hinnies (female donkey${\times}$male horse) and mules (female horse${\times}$male donkey) are sterile with few reports of equine fertile hybrids. The main cause of this sterility is thought to be a meiotic block to spermatogenesis and oogenesis. This study compared the developmental features of the testes and a histological analyses of spermatogenesis in a male hinny with those of a normal, fertile stallion and Jack donkey. Hinny testes showed a thicker tunica albuginea, fewer blood vessels and more connective tissue in the testis parenchyma than those of the stallion and Jack donkey. Although the mean number of seminiferous tubules was significantly higher in stallion and hinny than Jack donkey (p<0.01), the mean proportion of seminiferous tubules was lower in the hinny (p<0.01) which resulted in a smaller diameter of seminiferous tubules. The mean number of spermatogonia and spermatocytes per unit area were significantly lower in hinny testis (p<0.01) and no spermatids or mature spermatozoa cells were found during immunofluorescent analyses. These results indicated that defects in seminiferous tubule development and structure occur in the testis of hinnies. Furthermore, most spermatogonia and spermatocytes cease development in synapsis during mid-meiosis of spermatocytes, which results in a block to spermatogenesis that prevents the formation of spermatids and matured spermatozoa during meiosis in male hinnies.

Phosphamidon-induced apoptosis in the testis of chickens and rats (Phosphamidon 을 투여한 닭 및 랫트 고환의 Apoptosis 에 대한 연구)

  • Lee, Cha-Soo;Chung, Jae-Yong;Park, Sang-Joon;Jeong, Kyu-Shik
    • Korean Journal of Veterinary Pathology
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    • v.3 no.1
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    • pp.27-33
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    • 1999
  • Phosphamidon(PMD) is orgnophosphate insecticide broadly using in agriculture. In order to study PMD toxicity in the testis, histopathological change and apoptosis were assessed following acute and chronic oral administration in rats and chickens. In acute studies, histopathological changes included necrosis and desquamation of spermatogenic cells, multinucleated giant cells in the lumen of seminiferous tubules, and necrotic cells and the giant cells in the epididymal lumen. Atrophy of seminiferous tubule was seen in the chronic exposure with low doses. The toxic effects of PMD in chronic exposure including clinical signs and histopathological changes were more pronounced in chickens than rats. Apoptosis assessment was performed by TUNEL method and Hoechst staining. TUNEL-positive apoptotic cells were found in spermatocytes of seminiferous tubules, testicular apoptosis was more prominent following acute exposure than control and chronic exposure. Above mentioned result noticed that PMD causes apoptotic death and effects directly the spermatocytogenesis.

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Gonad Structure and Reproductive Cycle of the Smallmouth Scorpionfish, Scorpaena miostoma (Teleostei: Scorpaenidae) (쭈굴감펭 (Scorpaena miosfoma)의 생식소 구조 및 생식주기)

  • LEE Jung Sick;KANG Ju-Chan;HUH Sung-Hoi
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.30 no.4
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    • pp.627-633
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    • 1997
  • Gonad structure, germ cell development and reproductive cycle of the smallmouth scorpionfish, Scorpaena miostoma were investigated based on histological method. Samples were collected monthly in the vicinity of Suyoung Bay, Pusan, Korea from November 1995 to October 1996. The testis is seminiferous tubule type in internal structure. Seminiferous tubule consists of numerous testicular cysts which contain numerous germ cells in same developmental stage. The ovary consists of several ovarian lamellae originated from ovarian outer membrane. Oogonia originated from the inner surface of the ovarian lamella protrude to the ovarian cavity in oocyte stage, and they are suspended by the egg stalk. Biological minimum size of female and male were 12.5cm in total length. Gonadosomatic index (GSI) of female (3.81) and male (0.23) were the highest in October. Reproductive cycle was classified into the following successive stages: in female, growing stage $(May\~August)$, maturation stage $(September\~October)$, ripe and spawning stage $(November\~December)$, recovery and resting stage $(January\~April)$, and in male, growing stage $(June\~August)$, maturation stage $(September\~October)$, ripe and spent stage $(November\~January)$ and recovery and resting stage $(February\~May)$.

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Evaluation of Radiation-induced Apoptosis in Seminiferous Tubule of ICR Mouse after Gamma Irradiation. (감마선을 조사한 ICR 마우스 정세관에서 apoptosis 발생 평가)

  • Jang, Jong-Sik;Kim, Joong-Sun;Kim, Jong-Choon;Kim, Sung-Ho
    • Journal of Life Science
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    • v.19 no.6
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    • pp.799-803
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    • 2009
  • The killing of male germ cells by radiation and other toxicants has recently been attributed to apoptosis, but a critical evaluation of the presence of the different features of apoptosis in each epithelial stage has not been performed. In this study, mouse testes exposed to radiation were examined by light microscopy and terminal transferase-mediated end labeling (TUNEL) with periodic acid-Schiff (PAS) stains to determine whether the cells were apoptotic according to several criteria. Apoptosis was easily recognized by the presence of peroxidase-stained, entirely apoptotic bodies. In the TUNEL-positive cells or bodies, the stained products correlated precisely with the typical morphologic characteristics of apoptosis as seen at the light microscopic level. The changes that occurred from 0 to 24 hours after exposing the mice to 2 Gy of gamma-rays (2 Gy/min) were examined. The numbers of apoptotic cells reached a peak at 12 hours after irradiation and then declined. The mice that received 0-8 Gy of gamma-rays were examined 8 hours after irradiation. Dose-response relationships were generated for each stage of the epithelial cycle by counting TUNEL-positive cells. The dose-response curves were linear- quadratic [y=(-0.014${\pm}$0.009)$D^{2}$+(0.31${\pm}$0.697)D+0.3575. Where y=the number of apoptotic cells per seminiferous tubule, and D=the irradiation dose in Gy, $r^{2}$=0.9] and there was a significant relationship between the frequency of apoptotic cells and the radiation dose. Although the maximum response was produced by 8 Gy, even 0.5 Gy induced marked changes. These changes were most pronounced in B spermatogonia of stage V and the spermatocyte at the mitotic cells of stage XII.

Studies on testses development and spermatogenesis in dog (개의 정소발육과 정자발생에 관한 연구)

  • Lee, Jae-hong;Park, Young-seok;Lee, Seong-ho
    • Korean Journal of Veterinary Research
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    • v.31 no.4
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    • pp.355-365
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    • 1991
  • This study was conducted in order to observe the changes in cellular association of seminiferous tubules from 16 to 24 weeks of age and to obtain the cycle and relative duration of the seminiferous epithelia from 28 to 44 weeks of age in Korean native dogs. The results were summarized as follows; 1. Gonocytes were seen at 16 weeks of age, however they were not observed as from 20 weeks of age. Both type A and type B-spermatogonia occurred from 20 weeks, while primary spermatocytes were found from 20 weeks. Secondary spermatocytes and spermatids appeared from 28 weeks. Spermatozoa were observed at first at 28 weeks of age. 2. Type A-spermatogonia appeared approximately 1.6 times as many at stage II compared to stage I, while the same numbers of cells were seen in both stage I and VII, showing the least number among VIII stages of the cycle of the seminiferous epithelia. The type B-spermatogonia were found from stage VI to VIII, Leptotene phase of the primary spermatocyte divided from type B-spermatogonia in stage VII observed at the stage VIII. Pachytene phase of the primary spermatocytes were shown the least in number at stage IV. The secondary spermatocyte could be seen only at stage IV. 3. The relative frequency of each stage from stage I to VIII of the cycle of the seminiferous epithelia was 30.3, 12.0, 9.8, 4.2, 8.5, 10.5, 11.4 and 13.4% respectively. Thus the establishment of spermatogenesis in Korean native dog was completed from 28 weeks of age.

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Histological study on the injury of the seminiferous tubules of the pheasant(Phasianus colchicus) following 60Co γ-irradiation (60Co 감마선 조사에 의한 꿩의 정세관 손상에 관한 조직학적 연구)

  • Lee, Dong-myung
    • Korean Journal of Veterinary Research
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    • v.34 no.4
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    • pp.665-678
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    • 1994
  • This study was undertaken to investigate histological changes according to the radiosensitivity in the spermatogenic cells in Korean native pheasants. During spermatogenetic period, testes wete collected from male adult Korean native pheasant and they were used as experimental and control birds. The experimental group was divided into a single-dose whole body irradiation group(400, 600, 800 and 1000 rads) and a split-dose whole body irradiation groups(400/2, 600/2, 800/2 and 1000/2 rads). A Henseky's $^{60}Co$ ${\gamma}$-radiotherapy machine was used for this experiment and the dose rate of $^{60}Co$ ${\gamma}$-ray was 104 rads/min. The experimental birds were sacrificed at 24 and 72 hrs after irradiation and the control pheasants were sacrificed at the same time. General histological changes of seminiferous epithelial cells were observed by hematoxylin-eosin stain with light microscope. The results obtained are summarized as follows ; 1. In the single-dose and the split-dose irradiation groups, the average diameter of the seminiferous tubule was decreased compared with control group. 2. Seminiferous epithelial cells were more severely damaged after 72 hrs than after 24 hrs of single-dose irradiation of 400, 600 and 800 rads but the difference of cell injury was almost not observable with the elapsed time in the group of the single-dose irradiation of 1000 rads. 3. The damage of spermatogenic cells were more severe after 24 hrs than after 72 hrs of the split-dose irradiation of 400 rads but the split-dose irradiation of 600, 800 and 1000 rads were more severe after 72 hrs than after 24 hrs.

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Scanning Electron Microscopic Study of the Sertoli Cell in the Korean Native Bull (한우 Sertoli 세포의 주사전자현미경적 연구)

  • 이성호;박영석
    • Journal of Veterinary Clinics
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    • v.16 no.2
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    • pp.448-453
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    • 1999
  • The three-dimensional structure of the Sertoli cell in the Korean native bull was investigated by scanning electron microscopy. Morphologically, four types of Sertoli cell processes were evident: 1) sheet-like processes, 2) sleeve-like processes, 3) bough-like processes and 4) finger-like processes. The sheet-like processes rested upon more than half of the surface of each spermatogonia, spermatocyte and spermatid. Sleeve-like processes, bough-like processes and finger-like processes are observed in the middle and apical portion of seminiferous tubule. All Sertoli cell processes are originated from Sertoli cell column. Just before spermiation, the apical sheet-like processes are shifted from their position at the spermatid head, and bough-like processes covered the disengaged residual body, after which the residual body was no longer evident in the tubule. Though the mechanism for this elimination is not known, the process suggests a reciprocity between the Sertoli and germ cells.

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Effect of GnRH Immunization on Testicular Function in Colts

  • Tshewang, U.;Dowsett, K.F.;Knott, L.;Jackson, A.
    • Asian-Australasian Journal of Animal Sciences
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    • v.12 no.3
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    • pp.348-353
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    • 1999
  • Ten Australian Stock Horses colts (five yearling and five 3-year old colts) of which 2 yearlings and 2 three year old colts served as control animals while 3 yearlings and 3 three year old colts received two GnRH immunizations within 4 weeks interval were used in this study. By the 5th to 6th week after immunization, the GnRH antibody titres in the plasma rose above 1:1000 and attained peak levels of 1:6500 by the 8th week and gradually declined to about 1:3000 by the 10th week in both the age groups. The testosterone and androstenedione concentrations of the control colts in both age groups were significantly greater (p<0.05) than that of the vaccinated groups. During the immunosuppression period, the vaccinated colts behaved like geldings. Semen could not be collected from 2 of the 3 three-year old vaccinated colts. The testicular dimensions, testicular weight, parenchymal weight, seminiferous tubule volumes, interstitial space volumes, Leydig cell volume, seminiferous tubule % of the control colts were significantly greater than those of the vaccinated colts in both the age groups. The 3-year old control colts had a significantly (p<0.05) greater % of Leydig cells than the control and vaccinated 1-year old colts. There was arrest of spermatogenesis with complete absence of sperm in the testes of the vaccinated colts while there was various stages of spermatogenesis in those of the control colts. Morphometric analysis demonstrated that the 3-year old colts had significantly (p<0.05) greater DSP/gm of testis and DSP/testis than those of the 1-year old control colts. This study elucidated that the GnRH immunization could suppress the testicular function of the 3-year old and yearling colts.

Reproductive Cycle and Gonadal Development of the Naked-Headed Goby, Favonigobius gymnauchen (Teleostei : Gobiidae) (날개망둑 (Faronigobius gymnauchen)의 생식주기 및 생식소 발달)

  • LEE Jung Sick;KIM Jae Won;KANG Ju-Chan;SHIN Yun Kyung;CHIN Pyung
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.33 no.3
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    • pp.219-224
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    • 2000
  • Reproductive biology of the naked-headed goby, Faronigobius gymnauchen was investigated by means of histological methods. The ovary was consisted of several ovarian lamellae and the oogonia originated from the inner surface of the ovarian lamella. The testis was seminiferous tubule One in internal structure. Seminiferous tubule was consisted of many testicular cysts which contained numerous germ cells in a same developmental stage. The size of group maturity was 4.5 cm intotal length. Gonadosomatic index(GSI) of the female and male was the highest in June and July, respectively. Reproductive cycle could be classified into the growing ($January{\~}March$), maturation ($April{\~}May$), ripe and spent (June{\~}July$), and recovery and resting ($August{\~}December$). Oocyte development was group-synchronous, and yolk nucleus was observed in the early growing oocyte.

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