• 제목/요약/키워드: In vitro culture of embryo

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기내 수분과 배양에 의한 화본과 사료작물 종속간 수정과 배의 발육 (Fertilization and Embryo Development in Pollination and Culture for Interspecific and Intergeneric Crossing of Forage Crops)

  • 이호진;한지연
    • 한국작물학회지
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    • 제32권4호
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    • pp.455-461
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    • 1987
  • Festuca속의 토올페스큐와 메도우페스큐, 그리고 Lolium속의 이탈리안라이그라스들 간에 종속간 잡종을 얻기 위하여 기내수분과 기내배양을 실시하였다. 이들 작물들의 자방과 화분을 채취하여 소독을 하고 주두수분, 주두제거 수분, 배주수분의 3가지 방법으로 기내수분을 실시하였다. 그리고 이들의 배발육상태를 MS, N6 , White's의 배지종류와 IAA Kinetln, BA의 생장조절물질의 처리로서 비교하였다. 1. 토올페스큐, 메도우페스큐, 이탈리안라이그라스의 상호 조합간 기내수분에서 44~92%의 수정율을 나타내었다. 이들의 주두수분은 평균 67.8% 주두제거 수분은 평균 89%의 수정율을 보였으나 배주수분은 평균 61 %로 낮았다. 2. 화본과 수정배주에서 배발육을 촉진하는데는 White's 배지가 가장 효율적이었고 식물생장조절물질의 처리는 IAA(10mg/$\ell$)와 Kinetin(0.2 mg/$\ell$)의 혼합처리가 무처리보다 효과적이었으나 발아율은 극히 저조하였다 3. 기내배양으로 성숙 배주의 배부조직에서 유관책의 형성과 시원체조직의 분화를 확인할 수 있었으며 배주 내부에 후막세포들의 형성이 관찰되었다.

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Evaluation of human embryo development in in vitro fertilization- and intracytoplasmic sperm injection-fertilized oocytes: A time-lapse study

  • Kim, Hyung Jun;Yoon, Hye Jin;Jang, Jung Mi;Lee, Won Don;Yoon, San Hyun;Lim, Jin Ho
    • Clinical and Experimental Reproductive Medicine
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    • 제44권2호
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    • pp.90-95
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    • 2017
  • Objective: We investigated whether the insemination method (in vitro fertilization [IVF] or intracytoplasmic sperm injection [ICSI]) affected morphokinetic events and abnormal cleavage events in embryonic development. Methods: A total of 1,830 normal fertilized embryos were obtained from 272 IVF and ICSI cycles that underwent ovum retrieval culture using a time-lapse system (Embryoscope) from June 2013 to March 2015. All embryos were investigated by a detailed time-lapse analysis that measured the developmental events in the hours after IVF or ICSI insemination. Results: No significant differences were observed between the two groups regarding clinical outcomes (p>0.05). ICSI-derived embryos showed significantly faster morphokinetics than those derived from conventional IVF, from the time to pronuclear fading to the time to 6 cells (p<0.05). However, no significant differences were found from the time to 7 cells to the time to expanded blastocyst (p>0.05). There were no differences in abnormal cleavage events between the two groups (p>0.05); they showed the same rates of direct cleavage from 1 to 3 cells, 2 multinucleated cells, 2 uneven cells, and reverse cleavage. Conclusion: The morphokinetics of embryo development was found to vary between IVF- and ICSI-fertilized oocytes, at least until the 6-cell stage. However, these differences did not affect the clinical outcomes of the embryo. Additionally, no significant differences in abnormal cleavage events were found according to the fertilization method.

Clinical factors that affect the pregnancy rate in frozen-thawed embryo transfer in the freeze-all policy

  • Hwang, Seo Yoon;Jeon, Eun Hye;Kim, Seung Chul;Joo, Jong Kil
    • Journal of Yeungnam Medical Science
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    • 제37권1호
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    • pp.47-53
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    • 2020
  • Background: This study was conducted to analyze clinical factors that can affect pregnancy rates in normal responders undergoing the freeze-all policy in in vitro fertilization. Methods: We evaluated 153 embryo transfer cycles in 89 infertile women with normal response to controlled ovarian stimulation (COS). After COS, all embryos were cultured to the blastocyst stage, and good quality blastocysts were vitrified for elective frozen-thawed embryo transfer (FET). Clinical variables associated with COS and the results of COS and culture, including the number of retrieved oocytes, fertilized oocytes, and frozen blastocysts were compared between the pregnant group and the non-pregnant group. Results: After a single cycle of COS for each patient, 52 patients became pregnant while 37 did not. Significant differences were observed in the number of matured oocytes, fertilized oocytes, frozen blastocysts, and transferred embryos. The number of frozen blastocysts in the pregnant group was almost twice that in the non-pregnant group (5.6±3.1 vs. 2.8±1.9, p<0.001). The area under the receiver operating characteristic curve for the 4 frozen blastocysts was 0.801 in the pregnant group. Conclusion: In the freeze-all policy, the number of matured oocytes, number of fertilized oocytes, and number of frozen blastocysts might be predictive factors for pregnancy.

Embryogenic callus culture of Tribulus terrestris L. a potential source of harmaline, harmine and diosgenin

  • Nikam, T.D.;Ebrahimi, Mohammad Ali;Patil, V.A.
    • Plant Biotechnology Reports
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    • 제3권3호
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    • pp.243-250
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    • 2009
  • In the present study, a simple one medium formulation protocol for callus culture, somatic embryogenesis and in vitro production of ${\beta}-carboline$ alkaloids and diosgenin in Tribulus terrestris L. was developed. Extensive callus induction and proliferation was obtained in leaf explant on Murashige and Skoog (MS) medium supplemented with $5.0{\mu}M$ 6 benzyl adenine (BA) and $2.5{\mu}M$ ${\alpha}-naphthaleneacetic$ acid (NAA). The embryogenic callus was maintained on subculture to fresh parental medium at 4-week intervals over a period of 28 months. The frequency of embryo formation was at a maximum ($18.1{\pm}0.9$ per g of callus) on MS medium containing $5.0{\mu}M$ BA and $2.5{\mu}M$ NAA together with $75mg\;1^{-1}$ casein hydrolysate. Globular embryo developed into torpedo stage embryo under the influence of starvation. The accumulation of ${\beta}-carboline$ alkaloids (harmaline and harmine) and steroidal saponin (diosgenin) in non-embryogenic and embryogenic callus culture derived from leaf explant was compared with root, leaf, stem, and fruit of the mother plant. The embryogenic callus accumulated equivalent amounts of harmaline ($66.4{\pm}0.5{\mu}g/g$ dry weight), harmine ($82.7{\pm}0.6{\mu}g/g$ dry weight), and diosgenin ($170.7{\pm}1.0{\mu}g/g$ dry weight) to that of the fruit of T. terrestris. The embryogenic callus culture of this species might offer a potential source for production of important pharmaceuticals.

제주말에서 난포 크기에 따른 난포란의 체외성숙 (Effect of Follicle Size in Jeju Mare on Oocytes Matured in vitro)

  • 류재규;강태영
    • 한국임상수의학회지
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    • 제27권1호
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    • pp.46-49
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    • 2010
  • In this study, we investigated the number of follicles, oocyte recovery rate and oocyte competence after in vitro maturation according to the size of follicle. And equine oocyte competence after in vitro maturation was investigated in terms of the diameter of follicle with criteria of maturation: nuclear stage after Hoechst staining. The average number of follicles per ovary with middle size (11-20 mm, 2.68) was higher than those of small (5-10 mm, 0.74) and large size follicle (> 21 mm, 1.63), therefore medium follicle (53.1%) had higher proportion than other size of follicles. The average numbers of follicle per ovary was 5.05. The rate of oocyte recovery in small (54.5%) and middle follicle (50%) was higher than that in large follicle (40.9%). After culture for 48 h in Medium 199, 50%, 45.5%, and 44.4% of oocytes from the follicles with diameters of 5-10, 11-20, > 21 mm, respectively reached the metaphase II stage. This is the first report showing number of follicle, oocyte recovery rate according to follicular size, and in vitro oocyte maturation in Jeju mare in Korea. To fulfill in vitro equine embryo production, further studies such as the seasonal effect, in vitro fertilization etc is need.

Ferritin Light Heavy Chain 유전자가 도입된 인삼형질전환체의 단일배발생을 통한 식물체의 기내증식 (In vitro Propagation of Transgenic Ginsengs Introduced with Ferritin Light Heavy Chain Gene through Single Embryo Culture)

  • 윤영상;김종학;김무성;양덕춘
    • 한국자원식물학회지
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    • 제17권2호
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    • pp.161-168
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    • 2004
  • Ferritin light heavy chain (FLHC) gene는 일부 중금속과 결합, 저장 및 운반하여 무독화 시킬 수 있는 것으로 알려져 있다. Fe 관련 유전자인 FLHC유전자를 식물 발현용 promoter인 35S promoter와 Tnos를 사용하여 식물 형질전환용 vector를 재조합하였다. 식물세포형질전환용 binary vector는 상기 cassette vector가 조립이 매우 양호하며 border sequence를 가지고 있는 pRD400 binary vector를 사용하여 최종적으로 가나마이신 내성 유전자 (NPT II gene)와 tadpole ferritin heavy chain gene 및 human ferritin light chain gene를 함유하고 있는 binary vector를 재조합하였다. Binary vector의 아그로박테리움에 도입은 triparental mating 방법에 의하여 수행하여 AB배지 및 가나마이신 함유 배지에서 disarmed Ti-vector를 가지고 있는 Agrobacterium tumefaciens MP90/FLHC을 선발하였다. FLHC 유전자 도입된 식물형질전환용 binary vector를 이용하여 형질전환방법을 변형하여 많은 embryo를 유도하였으며 유도된 embryo들은 GA 10mg/L가 첨가된 배지에 지상부를 유도하였다. 형질전환체식물체의 정상적인 생장을 유도하기 위해 최적의 배양조건을 조사하였던 바, 비교적 1/3 MS배지에서 뿌리의 생장과 지상부의 생장이 균일하게 생장하는 경향을 보였으며, 뿌리와 줄기가 잘 발달된 약 7cm의 유식물체를 대량으로 증식하여, 모래와 흙이 1:1로 혼합된 토양에 옮겼다.

Amino Acids Supplemented with Culture Medium Stimulated On Development of Porcine Embryos

  • Lee, Y.S.;S.H. Song;Lee, S.N.;K.H. Chung;Park, C.S.
    • 한국수정란이식학회:학술대회논문집
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    • 한국수정란이식학회 2002년도 국제심포지엄
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    • pp.80-80
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    • 2002
  • This study was carried out that to investigate the effects of amino acids supplemented with culture medium on development of porcine embryos cultured in vitro. Cumulus oocyte complexes (COCs) were cultured in the maturation medium containing hormones (0.5$\mu\textrm{g}$/$m\ell$ LH, 0.5$\mu\textrm{g}$/$m\ell$ FSH and 1$\mu\textrm{g}$/$m\ell$ estradiol-17${\beta}$) for 20-22 h at 39$^{\circ}C$ in an atmosphere of 5% CO$_2$in air. Subsequently, COCs were cultured in hormone-free maturation medium for 20-22 h. After maturation for 40-44h, oocytes were removed cumulus cells by pipetting and cultured with epididymal sperm for 5 h in the mTBM. Embryos obtained were divided in 4 groups (1) cultured in NCSU 23 containing 0.4% BSA to blastocyst stage(Control), (2) essential amino acids (EA), (3) non-essential amino acids (NA), (4) mixture of essential and non essential amino acid (EA+NA). All treated groups(2-4) were used a glucose free NCSU 23 medium supplemented with pyruvate (0.33 mM), lactate (4.5 mM) to morula stage. From morula to blastocyst stage embryos of all treated groups were cultured in NCSU 23 containing 0.4% BSA. The rates of cleaved oocytes at 48 h after IVF were from 82% to 88% in the groups of control, EA, NA and EA+NA, respectively. The in vitro developmental rates into blastocysts in the groups of EA and EA+NA were significantly (P<0.05) higher than those of group of control (35.1, 35.4 vs. 19.4%, respectively), however, no significant (P<0.05) between control and NA. In conclusion, supplemented with essential amino acid or mixture of essential and non essential amino acid in the culture medium at morula stage increased the rate of development to blastocyst on in vitro produced porcine embryos.

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In Vitro Fertilization and Embryonic Development of Porcine Oocytes Matured in mSOF

  • J. M. Koo;S. H. Hyun;Lee, B. C.;S. K. Kang;W. S. Hwang
    • 한국수정란이식학회지
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    • 제17권3호
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    • pp.239-249
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    • 2002
  • Embryos derived from pig oocytes matured in mSOF are able to develop to blastocysts after IVF. Experiment 1 evaluated the effects of two maturation media (TCM-199 vs mSOF) on maturation rate, fertilization parameters, including penetration, polyspermy, male pronuclear formation, and the mean number of sperm penetrated per oocyte. Experiment 2 and Experiments 3 examined the effects of two maturation media on zona pellucida solubility and cortical granule distribution by transmissible electron microscopy, respectively. Experiment 4 assessed the effects of two maturation media on the in vitro embryo cleavage rate and development to blastocyst. Lastly, experiment 5 examined the cell number of blastocyst. An effect of media (P<0.05) was detected for mSOF on the mean number of sperm per oocyte. In TCM group, zona digestion time (196.5$\pm$15.5 vs 131.6$\pm$20.1 before IVF, 397.5$\pm$30.3s vs 185.3$\pm$16.4s after IVF, p<0.05) was higher in TCM-199 group. No significant effects of media was observed on cortical granule distribution between two groups by TEM. An effect (P<0.05) was observed on embryo development to blastocyst (16% vs 8%) but not on cleavage rates. No significant effects of media was observed on total cell number of blastocyst. We found that the high mean number of sperm penetrated per oocyte and the weaker zona pellucida on the basis of the digestion time was shown in pig oocytes matured in mSOF, however, porcine oocyte maturation with supplemented synthetic oviduct fluid medium (mSOF) resulted in blastocyst cell numbers comparable to those observed with Tissue Culture Medium 199.

Possible Improvement of Oocyte Supply by the use of Aged Mice and Different Gonadotrophins

  • Lee, Myungook;Ahn, Jong Il;Kwun, Hyosook;Ko, Dong Woo;Ahn, Jiyeon;Lim, Jeong Mook
    • 한국수정란이식학회지
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    • 제33권2호
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    • pp.69-73
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    • 2018
  • This study was conducted to examine the influences of two human chorion gonadotrophins (hCGs) being injected into young or aged (45- to 65-week old) outbred (ICR) mice on developmental capacity of oocytes retrieved. In vitro-culture and parthenogenetic activation of oocytes retrieved were employed for the assessment. Superovulation was determined as being induced when more than 25 oocytes were retrieved. No aged mice were superovulated, while in contrast, 67-100% were superovulated in the 6- to 8-week-old (young) mice. In the aged, hCG injection yielded better retrieval (5 vs. 13 to 14.8 oocytes/mouse). Overall, no significant difference between two hCGs was detected but between the young and aged, significant differences in maturational arrest (0% vs. 39% MI arrest and 46% vs. 15% degeneration) and developmental capacity (24% vs. 46% 8-cell embryo development) were detected. In conclusion, hCG injection contributes to increasing oocyte retrieval from aged outbred mice, but the kinds of gonadotrophin influenced the efficiency of hyperstimulation induction in specific ages.

미성숙 흰쥐에 있어서 과잉배란 난자의 체외수정 및 수정란의 배양에 관한 연구 (In Vitro Fertilization and Embryo Culture in Immature Rats induced to Superovulate)

  • 이종호;박충생
    • 한국가축번식학회지
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    • 제15권1호
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    • pp.41-47
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    • 1991
  • 미성숙 흰쥐에 있어서 과잉배란 유기시 PMSG용량이 체외수정에 의한 수정율과 수정란의 배양에 미치는 영향을 조사하고, 체외수정 및 배양용기로서 plastic mini-straw의 이용효과와 체외수정란의 이식성적을 조사한 바 다음과 같은 결과를 얻었다. 미성숙 흰쥐(체중 65~80g)에게 PMSG를 4, 10, 16 혹은 40IU를 1회 근육주사한 후 72시간에 채란한 난자 중에서 난구세포괴를 가진 정상형태의 난자와 정소상체 미부에서 채취하여 예비배양한 정자로 체외수정시켰다. 체외수정율은 PMSG 용량이 증가될수록 감소하였는데, 즉 4IU에서는 70.8%였으나, 40IU에서는 45.0%로 유의적으로 (P<0.05)저하하였다. 그러나 다정자 수정발생율은 2.3~9.7%로서 PMSG 용량에 따른 유의적인 증가는 없었다. 이 결과는 과량의 PMSG의 투여로 배란된 난자 중에서 일부는 비록 난자가 형태학적으로는 난구세포괴를 가지는 정상적인 난자일지라도 체외수정율의 저하는 정상적인 배란시간보다 조기배란으로 난자의 노화로 인하여 수정에 적합하지 않음을 제시하고 있다. 그리고 plastic mini-straw를 고안하여 straw내에서 체외수정시킨 후 66~72시간까지 배양시험한 결과 2-16와 4-16세포기까지 발달된 배의 비율은 petri dish보다 다소 우수(P<0.05)하였으며, straw용기에서 체외수정된 2세포기의 52개의 배를 7마리의 위임신 흰쥐에게 이식시켰던 바 6개의 배를 이식 받은 한 마리의 수란쥐가 2마리의 새끼를 분만하였다.

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