• 제목/요약/키워드: gonadal tissue

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북방전복 Haliotis discus hannai의 형태학적 성분화 (Morphological Sex Differentiation of the Abalone Haliotis discus hannai)

  • 김혜진;전미애;최지성;김병학;손맹현;이정식
    • 한국패류학회지
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    • 제31권4호
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    • pp.273-277
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    • 2015
  • 본 연구는 북방전복의 생식생물학적 정보를 제공하고 아울러 성의 인위적인 조절에 필요한 정보를 제공하기 위하여 수행하였다. 북방전복의 형태학적 성분화 과정은 크게 다음과 같이 5단계로 구분할 수 있었다. 1) 생식소 외막 형성 (FGOM) (${\leq}SL\;10.0{\pm}1.0mm$), 2) 장과 간췌장 사이의 결체조직에 시원생식세포 (PGCs: primordial germ cells) 출현 (PAC) 및 생식소 내강 형성 (FGC) (SL $15.0{\pm}2.0mm$), 3) 생식소 내강 상피층에 PGCs 출현 (PAG) (SL $18.0{\pm}2.0mm$), 4) 생식세포형성소낭 형성, 초기 난모세포 및 정원세포 출현 (FGOC) (SL $21.0{\pm}2.0mm$), 5) 형태학적 성분화 (MSD) (${\geq}SL\;23.0{\pm}2.0mm$). 조직학적 분석 결과, 각장 24.1-25.0 mm 그룹에서 북방전복의 성분화율은 90.0%였으며, 성비 (암:수)는 1:0.8로 나타났다.

해가리비, Amusium japonicum japonicum (GMELIN)의 연령과 성장에 관한 연구 (Studies on the Age and Growth fo Sun and Moon Scallop, Amusium japonicum japonicum (GMELIN))

  • 손팔원;하동수;노섬;장대수
    • 한국양식학회지
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    • 제9권4호
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    • pp.409-417
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    • 1996
  • 해가리비의 패각에 나타난 윤문을 이용한 연령과 성장 및 생태에 관한 몇 가지 특징을 검토한 결과는 다음과 같다. 서귀포를 중심으로한 제주도 남부해성에 주로 분포하고 있는 해가리비의 산난기는 수온이 $17\~20^{\circ}C$되는 10월에서 12월로 나타났고, 2회 이상 다회산난하는 것으로 판단된다. 분포수온은 $14\~23^{\circ}C$ 범위이고, 주 서식장소는 사이질인 수심 $30\~40$ m였다. 패각에 나타난 윤문형성 시기는 산란기와 일치되고 있었다. 해가리비의 각고성장은 비교적 빠른 것으로 나타났고, 1연패의 경우 각고 6.28 cm, 2연패의 경우는 9.07 cm로 나타났으며, 이론적인 최대 각고는 13.3 cm 였다. 체중의 증가는 1세때 18.8 g, 2세 60 g, 3세의 경우는 102.4 g으로 급격히 증가하고, 최대체중은 198.8 g인 것으로 나타나, 금후 자연채묘에 의하여 양식을 시도하였을 때, 충분한 산업적 가치가 있을 것으로 여겨진다.

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암컷 가무락조개, Cyclina sinensis의 난소 발달단계에 따른 폐각근 조직과 내장낭 조직의 생화학적 성분의 계절적 변화 (Seasonal Changes in Biochemical Components of the Adductor Muscle and Visceral Mass Tissues in the Female Cyclina sinensis, in Relation to Gonad Developmental Phases)

  • 정의영;박관하;김종배;이창훈
    • 한국패류학회지
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    • 제20권1호
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    • pp.85-92
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    • 2004
  • We investigated the reproductive cycle with gonadal development of the female Cyclina sinensis by histological observations and seasonal changes in biochemical components of the adductor muscle and visceral mass tissues were studied by biochemical analysis, from January to December, 2001. The reproductive cycle of this species can be classified into five successive stages: early active stage (February to April), late active stage (March to June), ripe stage (May to August), partially spawned stage (July to October) and spent/inactive stage (September to February). Total protein contents in the adductor muscle tissues reached the maximum in February (early active stage) and appeared the minimum in June (ripe stage), while their contents in the visceral mass tissues reached the maximum in the late active and ripe stages (June) and gradually decreased from July (partially spawned stage) to November (spent/inactive stage). Changes in total protein contents showed a negative correlationship between the adductor muscle and visceral mass tissues (r = -0.499, p = 0.099). Total lipid contents in the adductor muscle tissues reached the maximum in January (the inactive stages) and their contents gradually decreased from February. Their contents in the visceral mass tissues, however, reached the maximum in June (late active and ripe stage) and gradually decreased from July (the partially spawned stage). On the whole, total lipid contents showed a negative correlationship between the adductor muscle and visceral mass tissues (r = -0.631, p < 0.05). Therefore, These results indicate that the nutrient contents of the adductor muscle and visceral muscle tissues change in response to gonadal energy needs. Glycogen contents in the adductor muscle tissue reached the maximum in March (early and late active stages) and decreased from July to September (partially spawned stage). while their contents in the visceral mass tissues reached the maximum in June (late active and ripe stages) and gradually decreased from July (partially spawned stage). Thereafter, their levels gradually increased in November (spent/inactive stage). On the whole, changes in glycogen contents appeared negative correlationship between the adductor muscle and visceral mass tissues. However, they showed no significant different (r = -0.307, p = 0.331).

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담수산 진주패 뻘조개, Anodonta(Sinanodonta) woodiana(Lea)의 생식주기 및 임란기 (REPRODUCTIVE CYCLE AND BREEDING SEASON OF THE FRESHWATER CLAM, ANDONTA (SINANODONTA) WOODIANA(LEA))

  • 정의영
    • 한국수산과학회지
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    • 제13권4호
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    • pp.135-144
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    • 1980
  • 우리나라 낙동강 하류에 서식하는 뻘조개, Anodonta (Sinanodonta) woodiana의 생식소발달 과정 및 생식주기 그리고 임란기 등을 조사하였다. 1. 생식소는 내장낭의 간중사선 하방으로부터 족부의 외벽근층내에 있는 섬유성 망상결제조직까지 분포되어 있다. 난소는 많은 난소소낭으로 구성되어 있는데, 이들 소낭의 내공상피가 생식상피 기능을 하고 있다. 2. 초기난소 몇 정소의 생식상피상에는 호산성 과립세포와 부분화 간충조직들이 풍부하게 나타나고 있으며, 이들은 생식소 발달과 함께 그 량이 감소하고 있다. 3. 산란은 고수온기인 8월과 9월을 제외하고 년중 일어나고 있는데 1월에서 3월과, 6월에서 7월의 2회에 걸쳐 성기를 나타내고 있다. 4. 보육낭내에 trochophore 유생을 임란한 개체는 8월과 9월을 제외하고 년중 나타났으며 glochidia 유생을 임란한 개체는 9월을 제외하고 연중 나타났는데, 5월이 $72.7\%$ 년중 가장 높은 임란율을 나타내고 있다.

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Gametogenic Cycle and the Spawning Season by Quantitative Statistical Analysis and the Biological Minimum Size of Cyclina sinensis in Western Korea

  • Chung, Ee-Yung;Lee, Chang-Hoon;Park, Young-Je;Choi, Moon-Sul;Lee, Ki-Young;Ryu, Dong-Ki
    • 한국패류학회지
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    • 제27권1호
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    • pp.43-53
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    • 2011
  • The gametogenic cycle and the spawning season in female and male Cyclina sinensis were investigated by quantitative statistical analysis using an image analyzer system, and the biological minimum size (the size at 50% of sexual maturity) was calculated by combination of quantitative data by size and von Bertalanffy's equation. Compared the gametogenic cycle by quantitative statistical analysis with the previous qualitative results in female and male C. sinensis, monthly changes in female and male gametogenic cycles calculated by quantitative statistical analysis showed similar patterns to the gonadal stages in female and male reproductive cycles by qualitative histological analysis. Comparisons of monthly changes in the portions (%) of each area to eight kinds of areas by quantitative statistical analysis in the gonads in female and male C. sinensis are as follows. Monthly changes in the portions (%) of the ovary areas to total tissue areas in females and also monthly changes in the portions of the testis areas to total tissue areas in males increased in March and reached the maximum in May, and then showed a rapid decrease from June to October. Monthly changes in the portions (%) of oocyte areas to ovarian tissue areas in females and also monthly changes in the portions of the areas of the spermatogenic stages to testis areas in males began to increase in March and reached the maximum in June in females and males, and then rapidly dropped from July to October in females and males when spawnig occurred. From these data, it is apparent that the number of spawning seasons in female and male C. sinensis occurred once per year, from July to October. Monthly changes in the number of the oocytes per mm2 and in the mean diameter of the oocyte in captured image which were calculated for each female slide showed a maximum in May and reached the minimum from December to February. Therefore, C. sinensis in both sexes showed a unimodal gametogenic cycle during the year. The percentage of sexual maturity of female and male clams ranging from 25.1 to 30.0 mm in length was over 50% and 100% for clams over 40.1 mm length. In this study, the biological minimum size (sexually mature shell lengths at 50% of sexual maturity) in females and males were 26.85 and 26.28 mm, respectively.

Differential Growth of the Reproductive Organs during the Peripubertal Period in Male Rats

  • Han, Seung Hee;Lee, Sung-Ho
    • 한국발생생물학회지:발생과생식
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    • 제17권4호
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    • pp.469-475
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    • 2013
  • In mammals, puberty is a process of acquiring reproductive competence, triggering by activation of hypothalamic kisspeptin (KiSS)-gonadotropin releasing hormone (GnRH) neuronal circuit. During peripubertal period, not only the external genitalia but the internal reproductive organs have to be matured in response to the hormonal signals from hypothalamic-pituitary-gonadal (H-P-G) axis. In the present study, we evaluated the maturation of male rat accessory sex organs during the peripubertal period using tissue weight measurement, histological analysis and RT-PCR assay. Male rats were sacrificed at 25, 30, 35, 40, 45, 50, and 70 postnatal days (PND). The rat accessory sex organs exhibited differential growth patterns compared to those of non-reproductive organs. The growth rate of the accessory sex organs were much higher than the those of non-reproductive organs. Also, the growth spurts occurred differentially even among the accessory sex organs; the order of prepubertal organ growth spurts is testis = epididymis > seminal vesicle = prostate. Histological study revealed that the presence of sperms in seminiferous tubules and epididymal ducts at day 50, indicating the puberty onset. The number of duct and the volume of duct in epididymis and prostate were inversely correlated during the experimental period. Our RT-PCR revealed that the levels of hypothalamic GnRH transcript were increased significantly on PND 40, suggesting the activation of hypothalamic GnRH pulse-generator before puberty onset. Studies on the peripubertal male accessory sex organs will provide useful references on the growth regulation mechanism which is differentially regulated during the period in androgen-sensitive organs. The detailed references will render easier development of endocrine disruption assay.

생쥐의 생식소 분화과정중 난소내 Gonadotropin-Releasing Hormone 유전자의 발현 (Expression of Gonadotropin-Releasing Hormone Gene in Mouse Fetal Ovary during Gonad Differentiation)

  • 윤성희
    • 한국발생생물학회지:발생과생식
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    • 제1권2호
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    • pp.189-202
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    • 1997
  • The hypothalamic peptide GnRH plays a central role in the regulation of the mammalian reproductive axis. Recent studies suggested that GnRH stimulates or inhibits the ovarian steroidogenesis and gametogenesis directly. Our previous report indicated that GnRH gene is expressed in adult rat ovary as well as in hypothalamus and that the expressed GnRH may induce the follicular atresia and apoptosis of ovarian granulosa cells in rat. Therfore, we studied whether GnRH gene is expressed in the mouse fetal ovary, when the germ cells are degenerating by apoptosis during gonad diffeerentiation. Mouse fetal gonads were obtained on the 12, 15,18 and 20th day of gestation from the mother mice superovulated (10 IU PMSG and 10 IU hCG) and mated. The morphological changes of fetal ovaries were examined histochemically by hematoxylin-eosin staining. The fetal sex was confirmed by PCR methods for sexing. RT-PCR methods were used to examine the expression of GnRH gene and the sex steroid hormones were determined by conventional radioimmunoassays. The levels of estradiol (E) and progesterone (P) were increaseduntil 18th day of gestation and then E was decreased just before parturition. The morphological changes of fetal gonadal tissue sections showed the ovarian development and coincided with the result of PCR analysis for sexing using ovary- or testis- specific oligonucleotide primers. Immunoreactive GnRH in placenta was decreased gradually until the end of gestation but fetal brain and ovarian GnRH were increased. The level of GnRH gene expression was increased during fetal ovarian development from 12 till 18th day and decreased suddenly on 20th day just before birth. From these results, it is suggested that ovarian GnRh may play a regulatory role on the germ cell differentiation of fetal ovary.

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Anti-Mullerian Hormone Serum Concentrations in Prenatal and Postnatal Period in Murine

  • Kim, Dae Young
    • 한국수정란이식학회지
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    • 제28권2호
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    • pp.149-155
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    • 2013
  • Mullerian inhibiting substance (MIS) is a member of the TGF-${\beta}$ (transforming growth factor-${\beta}$) family whose members play key roles in development, suppression of tumour growth, and feedback control of the pituitary-gonadal hormone axis. MIS is expressed in a highly tissue-specific manner in which it is restricted to male Sertoli cells and female granulose cells. The serum levels of MIS in prenatal and postnatal ICR mice were measured using the enzyme-linked immuno-solvent assay (ELISA) using the MIS/AMH antibody. Mice were grouped by age: the significant periods were at the onset of development. During sex organ differentiation, no remarkable difference between female and male foetus MIS serum levels (both<0.1 ng/ml) was observed. However, MIS serum levels in pregnant mice markedly changed (4.5~12.2 ng/ml). After birth, postnatal female and male mice serum MIS levels changed considerably (male: <0.1~138.5 ng/ml, female: 5.3~103.4 ng/ml), and the changing phase were diametrically opposed (male: decreasing, female: fluctuating). These findings suggest that MIS may have strong associations with not only develop-ment but also puberty. For further studies, establishing the standard MIS serum levels is of importance. Our study provides the basic information for the study of MIS interactions with reproductive organ disability, cancer, and the effect of other hormone or menopause. We hypothesise that if MIS is regularly injected into middle-age women, meno-pause will be delayed. We detected that serum MIS concentration curves change with age. The changing phase is different between males and females, and this difference is significant after birth. Moreover, MIS mRNA is expressed during the developmental period (prenatal) and also in the postnatal period. This finding indicates that MIS may play a significant role in the developmental stage and in growth after birth.

A sclerosing stromal tumor of the ovary with masculinization in a premenarchal girl

  • Park, Soo-Min;Kim, Young-Nam;Woo, Young-Jong;Choi, Ho-Sun;Lee, Ji-Shin;Heo, Suk-Hee;Kim, Chan-Jong
    • Clinical and Experimental Pediatrics
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    • 제54권5호
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    • pp.224-227
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    • 2011
  • A sclerosing stromal tumor of the ovary is an extremely rare benign tumor; it usually is found during the second and third decades of life. Patients present with pelvic pain or a palpable abdominal mass. Hormonal effects such as masculinization are uncommon. Here, an 11-year old premenarchal girl presented with deepening of the voice. In addition, clitoromegaly and hirsutism with a male suprapubic hair pattern were observed. The laboratory findings showed that the testosterone level was elevated to 3.67 ng/ml, andostenedione to above 10 ng/ml, dehydroepiandrosterone-sulfate to 346 ${\mu}g$/dl and 17-hydroxy progesterone (17-OHP) to 11.28 ng/ml. The chromosome evaluation revealed a 46,XX female karyotype. An adrenocorticotropic hormone stimulation test was performed. The 17-OHP to cortisol ratio in 30 minutes was 0.045, which suggested a heterozygote for the 21-hydroxylase deficiency. However, the CYP21A2 gene encoding steroid 21-hydroxylase showed normal. The pelvic ultrasound showed a heterogeneous mass consisting of predominantly solid tissue in the pelvic cavity. The pelvic magnetic resonance imaging revealed an $8.9{\times}6.2{\times}6.6$ cm mass of the left ovary. A left oophrectomy was performed and microscopic examination confirmed a sclerosing stromal tumor. Immunohistochemical studies showed that the tumor was positive for smooth muscle actin and vimentin, but negative for S-100 protein and cytokeratin. Following surgery, the hormone levels returned to the normal range and the hirsutism resolved.

The Tissue Distribution of Nesfatin-1/NUCB2 in Mouse

  • Kim, Jinhee;Chung, Yiwa;Kim, Heejeong;Im, Eunji;Lee, Hyojin;Yang, Hyunwon
    • 한국발생생물학회지:발생과생식
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    • 제18권4호
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    • pp.301-309
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    • 2014
  • Nesfatin-1, an anorexic nucleobindin-2 (NUCB2)-derived hypothalamic peptide, controls appetite and energy metabolism. Recent studies show that nesfatin-1/NUCB2 is expressed not only in the brain but also in gastric and adipose tissues. Thus, we investigated the distributions of nesfatin-1/NUCB2 in various tissues of male and female mice by real-time PCR, western blotting, and immunohistochemical staining. Real-time PCR analyses showed that NUCB2 mRNA was predominantly expressed in the pituitary and at lower levels in the hypothalamus, spleen, thymus, heart, liver, and muscle of both male and female mice. Expression was much higher in reproductive organs, such as the testis, epididymis, ovary, and uterus, than in the hypothalamus. Western blot analysis of the nesfatin-1 protein level showed similar results to the real-time PCR analyses in both male and female mice. These results suggest that nesfatin-1/NUCB2 have widespread physiological effects in endocrine and non-endocrine organs. In addition, immunohistochemical staining revealed that nesfatin-1 was localized in interstitial cells, including Leydig cells and in the columnar epithelium of the epididymis. Nesfatin-1 was also expressed in theca cells and interstitial cells in the ovary and in epithelial cells of the endometrium and uterine glands in the uterus. These results suggest that nesfatin-1 is a novel potent regulator of steroidogenesis and gonadal function in male and female reproductive organs. Further studies are required to elucidate the functions of nesfatin-1 in various organs of male and female mice.