• 제목/요약/키워드: Follicular Growth

검색결과 150건 처리시간 0.022초

OPU 채란계절이 한우의 난자 품질 및 발달 능력에 미치는 영향 (Effect of Collection Seasons on the Oocyte Quality and Developmental Competence of Oocytes Derived from Korean Native Cows (Hanwoo) by Ovum Pick-Up)

  • 김성수;최병현;조현태;진종인;하아나;민찬식;조규완;공일근
    • 한국수정란이식학회지
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    • 제29권3호
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    • pp.265-271
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    • 2014
  • 본 연구에서 한우를 공란우로 사용하여 OPU 방법으로 가장 더운 계절의 hot season과 선선한 cool season의 두 계절의 차이에 따른 생성된 난포의 수, 난자 회수율, 난자 등급율, 수정율 및 배반포 발달 능력을 분석하여, 두 계절이 공란우의 번식 능력에 미치는 영향에 관하여 조사하였다. 1. 계절의 영향이 OPU 공란우의 난포 생성 수에 미치는 결과는 난포 생성 개수는 1154개($18.32{\pm}2.26$), 971개($15.41{\pm}3.34$)로 hot season 그룹이 유의적으로 높은 것을 알 수 있었다(p<0.05). 2. 계절에 따른 난자 수 및 난자 회수율은 hot season 그룹의 475개($7.54{\pm}3.14$), 41.16%로 cool season 그룹 448개($7.11{\pm}3.42$), 46.14%와 비교하여 유의적인 차이가 없었다(p<0.05). 3. OPU를 통하여 회수된 두 계절별 난자 등급은 Grade A는 Hot season 그룹 110개($1.75{\pm}1.86$), Cool season 그룹 63개($1.00{\pm}1.46$)로 hot season 그룹이 cool season 그룹과 비교하여 유의적으로 높았다(p<0.05). 하지만 다른 등급인 Grade B는 87개($1.38{\pm}1.60$) vs. 97개($1.54{\pm}1.39$), Grade C는 166개($2.63{\pm}2.43$) vs. 170개($2.70{\pm}2.04$), Grade D는 112개($1.78{\pm}2.65$) vs. 118개($1.87{\pm}1.86$)로 hot season과 cool season 간의 유의적인 차이를 보이지 않았다(p<0.05). 4. 계절에 따른 체외 수정 후의 수정률은 hot season과 cool season 각각 242(66.67%)와 209(63.3%), 배반포 발달율 214(58.95%) vs. 188(56.97%)로 수정률과 배반포 발달율은 유의적인 차이가 없었다(p<0.05). 본 연구의 결과로 계절에 따른 영향에 의해 공란우의 난포생성수와 A등급의 난자 출현율에서 유의적인 차이를 보였다. 하지만 나머지 등급의 난자 출현율, 수정률 및 배반포 발달율은 차이가 없는 것으로 보아, 계절의 차이로 인한 한우 공란우의 번식 능력에 미치는 영향은 미비하다고 판단된다.

병아리에서 Heterophuopsis continua의 충체 회수율 및 성장 발육 (Recovery rate, growth and development of Heterophyopsis continua in experimental chicks)

  • 홍성종;이순형
    • Parasites, Hosts and Diseases
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    • 제28권1호
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    • pp.53-62
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    • 1990
  • H. continua는 조류 및 포유동물의 소장에 기생하는 이형흡충과의 장흡충이며 농어, 숭어 등 반염수어가 제 2 중간숙주이다. 우리 나라에서는 4례의 인체 감염례가 보고되었다. 이 연구는 H. continua의 실험적 종숙주로서 병아리의 적합성을 알기 위하여 시행하였다. 농어에서 인공소화법으로 수집한 H. continua의 피낭유충을 병아리에 경구 감염시키고 1, 2, 3, 4, 6, 8, 14 및 28일 후에 도살하여 소장과 맹장에서 충체를 회수하였다. 회수된 충체를 10% neutral formalin으로 고정하고 Semichon's acetone으로 염색하여 현미경으로 관찰, 계측하였다. 충체 회수율은 평균 12.8%이었으며 감염 제 4일까지는 높게 유지되었으나 그 이후 28일까지 빠른 속도로 감소하였다. 회수된 충체의 91.9%는 회장에서 수집되어 병아리에서 회장이 주 기생 부위임을 알게 되었다. 피낭유충에는 비생식기관인 구.복흡반, 인두, 식도 등이 상당히 발달되어 있었으며, 생식기관인 난소, 저정낭, 수정낭, 전.후고환 및 생식흡반 등도 계측할 수 있을 정도로 윤곽을 나타내고 있었다. 감염 제 1일에는 Mehlis 선이 출현하였으며, 제 2일에는 저정낭 후방의 표퍼하조직에 여포상의 난황소가, 난소 둘레에는 자궁이 나타났다. 감염 제 3일에 자궁 내에 충란이 형성되었으며 제 28일까지 계속해서 그 수가 증가하였다. 피낭유충은 실험기간동안 계속 성장하여 감염 제 28일에는 체장 $2,990{\;}{\mu\textrm{m}}$, 체폭 $525{\;}{\mu\textrm{m}}$이 되었다. 생식기관들의 발육은 감 염초기에 빠르게 진행되고 감염 후기에는 완만하게 28일까지 계속되어 일반적인 성장곡선의 후반부를 보여 주었다. 비생식기관들은 전 실험기간에 걸쳐 매우 완만하게 서서히 크기가 커졌다. 본 실험을 통하여 병아리를 비교적 적합한 실험적 종숙주로 추가하게 되었다.

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돼지난자의 체외성숙시 Transforming Growth Factor$\beta$와 난구세포의 상호작용 (Interaction between Transforming Growth Factor $\beta$ and Cumulus Cells during In Vitro Maturation in Porcine Oocytes)

  • 신명균;조재원;정희태;양부근;김정익;박춘근
    • 한국가축번식학회지
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    • 제22권1호
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    • pp.73-80
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    • 1998
  • 본 연구는 돼지난자의 체외성숙에 미치는 transforming growth factor $\beta$(TGF $\beta$)와 난수세포의 역할에 대하여 검토하였다. 난자의 체외성숙시 TGF $\beta$를 여러 농도에서 첨가한 경우 metaphase II로 성숙한 난자의 비율은 52~69%로 유의적인 차이는 나타내지 않았다. 성숙배양 24시간에서 난구세포의 유무에 관계없이 TGF $\beta$가 무첨가된 배양액 내에서는 성숙된 난자가 관찰되지 않았으나 TGF $\beta$첨가(5 및 4%)의 경우 성숙난자가 관찰되었다. 그러나, 성숙배양 48시간후 난자의 성숙율은 난구세포가 부착되어 있는 경우 TGF $\beta$첨가(70%)가 무첨가(52%)에 비해 높았으며, 난구세포를 세포를 제거한 경우 (35 및 26%)에 비해 유의적으로 높은 성숙율을 나타냈다(P<0.05). 한편, 나구세포가 부착된 난자의 성숙배양시 TGF $\beta$의 첨가시기에 의한 성숙율(54~71%)에는 큰 차이가 없었으나, 난구세포를 제거한 경우 전반기(59%) 또는 후반기(57%) 24시간 동안 TGF $\beta$를 첨가한 경우 48시간 동안 계속하여 첨가(27%) 또는 무첨가(38%)에 비하여 유의적으로 높은 성숙을 나타냈다(P<0.05). 이와 같은 결과는 난구세포가 돼지난자의 체외성숙시 필수적이지만, TGF $\beta$는 난구세포를 제거한 경우 난자의 성숙에 계속적인 역할을 하지 않는 것으로 추측된다.

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Platelet-Derived Growth Factor Receptor-α Subunit Targeting Suppresses Metastasis in Advanced Thyroid Cancer In Vitro and In Vivo

  • Lin, Ching-Ling;Tsai, Ming-Lin;Chen, Yu-hsin;Liu, Wei-Ni;Lin, Chun-Yu;Hsu, Kai-Wen;Huang, Chien-Yu;Chang, Yu-Jia;Wei, Po-Li;Chen, Shu-Huey;Huang, Li-Chi;Lee, Chia-Hwa
    • Biomolecules & Therapeutics
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    • 제29권5호
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    • pp.551-561
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    • 2021
  • Thyroid cancer is the most common endocrine malignancy. Patients with well-differentiated thyroid cancers, such as papillary and follicular cancers, have a favorable prognosis. However, poorly differentiated thyroid cancers, such as medullary, squamous and anaplastic advanced thyroid cancers, are very aggressive and insensitive to radioiodine treatment. Thus, novel therapies that attenuate metastasis are urgently needed. We found that both PDGFC and PDGFRA are predominantly expressed in thyroid cancers and that the survival rate is significantly lower in patients with high PDGFRA expression. This finding indicates the important role of PDGF/PDGFR signaling in thyroid cancer development. Next, we established a SW579 squamous thyroid cancer cell line with 95.6% PDGFRA gene insertion and deletions (indels) through CRISPR/Cas9. Protein and invasion analysis showed a dramatic loss in EMT marker expression and metastatic ability. Furthermore, xenograft tumors derived from PDGFRA geneedited SW579 cells exhibited a minor decrease in tumor growth. However, distant lung metastasis was completely abolished upon PDGFRA gene editing, implying that PDGFRA could be an effective target to inhibit distant metastasis in advanced thyroid cancers. To translate this finding to the clinic, we used the most relevant multikinase inhibitor, imatinib, to inhibit PDGFRA signaling. The results showed that imatinib significantly suppressed cell growth, induced cell cycle arrest and cell death in SW579 cells. Our developed noninvasive apoptosis detection sensor (NIADS) indicated that imatinib induced cell apoptosis through caspase-3 activation. In conclusion, we believe that developing a specific and selective targeted therapy for PDGFRA would effectively suppress PDGFRA-mediated cancer aggressiveness in advanced thyroid cancers.

Induction of Ski Protein Expression upon Luteinization in Rat Granulosa Cells

  • Kim, Hyun;Matsuwaki, Takashi;Yamanouchi, Keitaro;Nishihara, Masugi;Yang, Boh-Suk;Ko, Yeoung-Gyu;Kim, Sung-Woo
    • 한국수정란이식학회지
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    • 제26권4호
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    • pp.237-244
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    • 2011
  • Ski protein is implicated in proliferation/differentiation in a variety of cells. We had previously reported that Ski protein is present in granulosa cells of atretic follicles, but not in preovulatory follicles, suggesting that Ski has a role in apoptosis of granulosa cells. The alternative fate of granulosa cells other than apoptosis is to differentiate to luteal cells, however, it is unknown whether Ski is expressed and has a role in granulosa cells undergoing luteinization. Thus, the aim of the present study was to examine whether the initiation of luteinization with luteinizing hormone (LH) directly regulates expression of Ski in the luteinized granulosa and luteal cells after ovulation by in vitro models. RT-PCR and real time PCR analysis respectively revealed that LH had no effect on c-Ski mRNA expression in the cultured granulosa cells regardless of LH treatment. Though Ski protein is absent in granulosa cells of preovulatory follicle, its mRNA (c-Ski) was expressed and the level was unchanged even after LH surge. Taken together, these results demonstrated that Ski protein expression is induced in granulosa cells upon luteinization, and suggested that its expression is regulated post-transcriptionally. Moreover, expression of mRNA of Arkadia, an E3 ubiquitin ligases, in luteinizing granulosa cells in vivo was assessed by realtime-PCR. The levels of Arkadia mRNA expression were unchanged during follicular growth and postovulatory luteinization. These findings suggest that Ski protein level may be regulated during luteinization at translational and/or post-translational level but not by Arkadia.

Expression of Ski in the Corpus Luteum in the Rat Ovary

  • Kim, Hyun;Matsuwaki, Takashi;Yamanouchi, Keitaro;Nishihara, Masugi;Yang, Boh-Suk;Ko, Yeoung-Gyu;Kim, Sung-Woo
    • 한국수정란이식학회지
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    • 제26권4호
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    • pp.229-235
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    • 2011
  • Sloan-Kettering virus gene product of a cellular protooncogene c-Ski is an unique nuclear pro-oncoprotein and belongs to the Ski/Sno proto-oncogene family. Ski plays multiple roles in a variety of cell types, it can induce both oncogenic transformation and terminal muscle differentiation when expressed at high levels. Ski protein is implicated in proliferation/differentiation in a variety of cells. The alternative fate of granulosa cells other than apoptosis is to differentiate to luteal cells, however, it is unknown whether Ski is expressed and has a role in granulosa cells undergoing luteinization. Thus, the aim of this study was, by means of immunohistochemical methods, to locate Ski protein in the rat ovaries during ovulation and corpora lutea (CL) formation to predict the possible involvement of Ski in luteinization. In addition, we performed to examine whether the initiation of luteinization with luteinizing hormone (LH) directly regulates expression of Ski in the luteinized granulosa and luteal cells after ovulation by in vivo models. In order to examine the expression pattern of Ski protein along with the progress of luteinization, follicular growth was induced by administration of equine chorionic gonadtropin to immature female rat, and luteinization was induced by human chorionic gonadtropin treatment to mimic luteinizing hormone (LH) surge. While no Ski-positive granulosa cells were present in preovulatory follicle, Ski protein expression was induced in response to LH surge, and was maintained after the formation of corpus luteum (CL). These results indicate that Ski is profoundly expressed in the luteinized granulosa cells and luteal cells of CL during luteinization, and suggest that Ski may play a role in luteinization of granulosa cells.

여자체조선수의 영양생리학적 요인 개선을 위한 교육프로그램의 효과분석 (Implementation and Evaluation of a Nutrition Education Program to Improve the Nutritional an Physiological Status of Female Gymnasts)

  • 조성숙
    • 대한지역사회영양학회지
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    • 제5권1호
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    • pp.50-62
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    • 2000
  • This study was conducted with 20 female gymnasts to examine the relationship between eating patterns, diet menstrual function and hematological status. According to the baseline data a nutrition counseling and education program was developed and evaluated improved the nutritional status and health of female gymnasts. Mean body weight at the onset of the study was 42.1$\pm$7.0kg and was reduced to 41.8$\pm$6.1kg after the nutrition counseling and education program. The percent of body fat was significantly reduced from 13.9$\pm$3.7% to 13.1$\pm$3.1%(p<0.01) skinfold thickness of subscapular and thighs was reduced significantly(p<0.01, p<0.05) Mean daily intake levels of energy, protein calcium iron thiamin riboflavin and niacin were significantly elevated after the nutrition counseling and education program but were lower than the Recommenced Dietary Allowances. For the nutrition knowledge and food habits, the posttest mean scores showed a significant increase. The hematological status(hematocrit, serum ferritin) and the early follicle level of estradiol were elevated to a mild degree although it was not significant,. The follicular stimulating hormone level was elevated significantly(p<0.01) Gymnastica has been one of the sports implicated by the medical profession as having probable detrimental effects. The implications of such training to childs growth and maturation have yet to be determined . Most female athletes, however, experience poor nutritional status and delayed puberty The priorities were to prepared a more effective nutrition program and education material status and delayed puberty. The priorities were prepared a more effective nutrition program and educational material for athletes coaches and adminstrators to prepare guidelines for the team physicians and coaches to follow for the physical and physiological examinations of female athletes.

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Effect of Sphingosine-1-Phosphate on In Vitro Maturation of Porcine Oocytes

  • Lee, Hyo-Sang;Wee, Kap-In;Park, Jung-Sun;Han, Ji-Soo;Kong, Il-Keun;Koo, Deog-Bon;Kang, Yong-Kook;Lee, Kyung-Kwang;Han, Yong-Mahn
    • 한국동물번식학회:학술대회논문집
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    • 한국동물번식학회 2002년도 춘계학술발표대회 발표논문초록집
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    • pp.70-70
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    • 2002
  • Sphingosine-1-phosphate(S1P) is one of the sphingolipid metabolites which affect a variety of cellular processes including the proliferation, differentiation, growth, survival, migration and gene expression. The present study was undertaken to investigate the effect of SIP on nuclear maturation of porcine oocytes. In vitro maturation frequency of porcine oocytes were compared in three different media; group Ⅰ: NCSU23+0.1% PVA, group Ⅱ: NCSU23+10% PFF(porcine follicular fluid), and group Ⅲ: NCSU23+10% PFF+10 ng/㎖ EGF+2.5 mM β-mercaptoethanol. Each group containing 0.1 ㎎/㎖ cysteine was divided into 4 sub-groups of SIP concentration(0, 50, 500 and 5000nM). Porcine oocytes were incubated in each maturation medium supplemented with hormones(10 IU/㎖ PMSG and 10 IU/㎖ hCG) for 22h and then further cultured in the same medium without the hormones for 22h. After completion of in vitro maturation, the oocytes were fixed and stained to examine nuclear maturation by using a rapid stain method. In the group Ⅰ, the proportions of metaphase Ⅱ stage among oocytes cultured in 0nM(control), 50 nM, 500nM and 5000nM S1P were 45.5%, 66.7%, 56.6% and 48.7%, respectively. (omitted)

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Involvement of Ski Protein Expression in Luteinization in Rat Granulosa Cells

  • Kim, Hyun;Matsuwaki, Takashi;Yamanouchi, Keitaro;Nighihara, Masugi;Kim, Sung-Woo;Ko, Yeoung-Gyu;Yang, Boh-Suk
    • Reproductive and Developmental Biology
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    • 제35권3호
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    • pp.355-361
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    • 2011
  • Ski protein is implicated in proliferation/differentiation in a variety of cells. We had previously reported that Ski protein is present in granulosa cells of atretic follicles, but not in preovulatory follicles, suggesting that Ski has a role in apoptosis of granulosa cells. The alternative fate of granulosa cells other than apoptosis is to differentiate to luteal cells, however, it is unknown whether Ski is expressed and has a role in granulosa cells undergoing luteinization. Thus, the aim of the present study was to locate Ski protein in the rat ovary during luteinization to predict the possible role of Ski. In order to examine the expression pattern of Ski protein along with the progress of luteinization, follicular growth was induced by administration of equine chorionic gonadotropin to immature female rat, and luteinization was induced by human chorionic gonadotropin treatment to mimic luteinizing hormone (LH) surge. While no Ski-positive granulosa cells were present in preovulatory follicle, Ski protein expression was induced in response to LH surge, and was maintained after the formation of corpus luteum (CL). Though Ski protein is absent in granulosa cells of preovulatory follicle, its mRNA (c-ski) was expressed and the level was unchanged even after LH surge. Taken together, these results demonstrated that Ski protein expression is induced in granulosa cells upon luteinization, and suggested that its expression is regulated post-transcriptionally.

Transcriptome profile of one-month-old lambs' granulosa cells after superstimulation

  • Wu, Yangsheng;Lin, Jiapeng;Li, Xiaolin;Han, Bing;Wang, Liqin;Liu, Mingjun;Huang, Juncheng
    • Asian-Australasian Journal of Animal Sciences
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    • 제30권1호
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    • pp.20-33
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    • 2017
  • Objective: Superstimulatory treatment of one-month-old lambs can achieve synchronous development of numerous growing follicles. However, these growing follicles cannot complete maturation and ovulation. Oocyte maturation and competence are acquired during follicular development, in which granulosa cells play an essential role. Methods: In this study, we applied RNA sequencing to analyze and compare gene expression between prepubertal and adult superstimulated follicle granulosa cells in sheep. Results: There were more than 300 genes that significantly differed in expression. Among these differently expressed genes, many extracellular matrix genes (EGF containing Fibulin Like Extracellular Matrix Protein 1, pentraxin 3, adrenomedullin, and osteopontin) were significantly down-regulated in the superstimulated follicles. Ingenuity pathway and gene ontology analyses revealed that processes of axonal guidance, cell proliferation and DNA replication were expressed at higher levels in the prepubertal follicles. Epidermal growth factor, T-Box protein 2 and beta-estradiol upstream regulator were predicted to be active in prepubertal follicles. By comparison, tumor protein P53 and let-7 were most active in adult follicles. Conclusion: These results may contribute to a better understanding of the mechanisms governing the development of granulosa cells in the growing follicle in prepubertal sheep.