• Journal of Periodontal and Implant Science
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• 제26권1호
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• pp.1-26
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• 1996

This study was performed to estimate the effects of cultured bone cell inoculated on porous type hydroxyaptite for the regeneration of the artificial alveolar bone defect. In this experiment 3 beagle dogs were used, and each of them were divided into right and left mandible. Every surgical intervention were performed under the general anesthesia by using with intravenous injection of Pentobarbital sodium(30mg/Kg). To reduce the gingival bleeding during surgery, operative site was injected with Lidocaine hydrochloride(l:80,000 Epinephrine) as local anesthesia. After surgery experimental animal were feeded with soft dietl Mighty dog, Frisies Co., U.S.A.) for 1 weeks to avoid irritaion to soft tissue by food. 2 months before surgery both side of mandibular 1st premolar were extracted and bone chips from mandibular body were obtained from all animals. Bone cells were cultured from bone chips obtained from mandible with Dulbecco's Modified Essential Medium contained with 10% Fetal Bovine Serum under the conventional conditions. Porous type hydroxyapatite were immerse into the high concentrated cell suspension solution, and put 4 hours for attachin the cells on the surface of hydroxyapatite. Graft material were inserted on the artificial bone defect after 3 days of culture. Before insertion of cellinoculated graft material, scanning electronic microscopic observation were performed to confirm the attachment and spreading of cell on the hydroxyapatite surface. 3 artificial bone defects were made with bone trephine drill on the both side of mandible of the experimental animal. First defect was designed without insertion of graft material as negative control, second was filled with porous replamineform hydroxyapatite inoculated with cultured bone marrow cells as expermiental site, and third was filled with graft materials only as positive control. The size of every artificial bone defect was 3mm in diameter and 3mm in depth. After the every surgical intervention of animals, oral hygiene program were performed with 1.0% chlorhexidine digluconate. All of the animals were sacrificed at 2, 4, 6 weeks after surgery. For obtaining histological section, tissus were fixed in 10% Buffered formalin and decalcified with Planko - Rycho Solution for 72hr. Tissue embeding was performed in paraffin and cut parallel to the surface of mandibular body. Section in 8um thickness of tissue was done and stained with Hematoxylin - Eosin. All the specimens were observed under the light microscopy. The following results were obtained : 1. In the case of control site which has no graft material, less inflammatory cell infiltration and rapid new bone forming tendency were revealed compared with experimental groups. But bone surface were observed depression pattern on defect area because of soft tissue invasion into the artificial bone defect during the experimental period. 2. In the porous hydroxyapatite only group, inflammatory cell infiltration was prominet and dense connective tissue were encapsulated around grafted materials. osteoblastic activity in the early stage after surgery was low to compared with grafted with bone cells. 3. In the case of porous hydroxyapatite inoculated with bone cell, less inflammatory cell infiltration and rapid new bone formation activity was revealed than hydroxyapatite only group. Active new bone formation were observed in the early stage of control group. 4. The origin of new bone forming was revealed not from the center of defected area but from the surface of preexisting bony wall on every specimen. 5. In this experiment, osteoclastic cell was not found around grafted materials, and fibrovascular invasion into regions with no noticeable foreign body reaction. Conclusively, the cultured bone cell inoculated onto the porous hydroxyapatite may have an important role of regeneration of artificial bone defects of alveolar bone.

• Radiation Oncology Journal
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• 제17권2호
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• pp.158-165
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• 1999

목적 : 유방암 환자의 피부 섬유모세포를 이용한 in vitro 배양 실험을 통하여 16 세포집락 비율 분포의 변화를 관찰하여 16 세포집락 비율과 in vitro 세포 노화 및 섬유모세포 공여자의 in vivo 연령과의 연관성을 조사하고자 하였다. 대상 및 방법 :유방암 수술을 받은 3명의 환자로부터 얻은 유방부위 피부를 본 실험대상으로 사용하였다. 각 환자의 유방부위 피부로부터 얻은 피부 섬유모세포 표본의 명칭을 C1, C2, C3a 및 C3b로 분류하였으며 각 표본 공여자의 연령은 C1이 44세, C2는 54세, 그리고 C3a 및 C3b는 동일한 공여자로서 연령은 55세였다. 피부 섬유모세포의 단일세포 부유액은 일차조직 배양법으로 얻었으며 100 개의 세포들을 100m1 의 조직배양 flask에 분주 후 37$^{\circ}C$에서 2주 동안 배양하였다. 5개의 flask에서 배양한 피부 섬유모세포의 16 세포집락 비율을 알기 위하여 crystal violet으로 염색한 후 10 배율의 입체현미경을 이용하여 16개 세포 이상으로 구성된 세포집락수를 1개 이상으로 구성된 세포 집락수로 나눈 수치를 16 세포집락 비율로 나타내었으며 각각 5개의 flask에서 얻어진 16 세포집락 비율 평균치를 각 계대배양에 대한 16 세포집락 비율로 나타내었다. C1, C2의 계대배양 횟수는 각각 12회, 17회 였으며 C3a와 C3b는 14회 계대배양 하였다. 결과 : C1, C2, C3a 및 C3b 피부섬유모세포 모두에서 16 세포집락 비율이 계대배양 횟수의 증가에 따라 감소하는 경향을 보였으며, 집단이배화증가에 따라 감소하였다. 그리고 계대배양 횟수가 증가함에 따라 집단이배화가 증가되는 것이 관찰되었으며 특히 C3a 섬유모세포의 상관계수가 0.954(P=0.0001)로서 가장 강한 상관관계가 있음을 보였다 동일한 지점의 집단이배화에서 16 세포집락 비율이 고연령자인 C3a 공여자보다 저 연령자인 C1 공여자에서 더 높게 나타났다. 결론 : 사람 피부 섬유모세포의 in vitro 배양에서 계대배양 횟수의 증가에 따라 집단이배화는 증가되고, 세포 노화로 인해 16 세포집락 비율은 감소되는 것을 알 수 있었다. 또한 저연령의 피부 섬유모세포일수록 집단이배화 증가에 따른 16 세포집락 비율 감소가 고연령의 경우보다 완만하였다. 따라서 피부 섬유모세포 in vitro 배양에서 관찰되는 16 세포집락 비율은 in vitro 세포노화의 지표로서 유용하며 또한 피부 섬유모세포 공여자의 연령 평가에 이용될 수 있을 것으로 사료된다.

• 한국동물번식학회:학술대회논문집
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• 한국동물번식학회 2001년도 춘계학술발표대회
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• pp.22-22
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• 2001

To produce reconstituted rabbit embryos with fetal fibroblasts, the present study was evaluated the efficiencies of the different fusion and activation conditions as assessments of subsequent development and chromosome in the embryos. New Zealand White rabbits were used throughout the study. Fetal fibroblasts collected from 22-d of fetuses were cultured in DMEM ＋ 10% FBS in 5% $CO_2$ in air. The culture was maintained for 10 passages. In every passage half of cell suspension were kept In frozen. From rabbits treated with FSH in 30% PVP solution and hCG, oocytes were surgically collected from oviducts at 14 h post-hCG injection and stripped off their cumulus cells by re-pipetting in a 300 IU hyaluronidase solution. Oocytes with an extruded first polar body and dense cytoplasm were enucleated by micromanipulation in Ham's F-10 medium＋7.5 g/$m\ell$ cytochalasin B. Euncleation was confirmed under a fluorescence microscope after staining with 5 g/$m\ell$ bisbenzimide for 2 min. Each enucleated oocyte was injected with a fetal fibroblast into a perivitelline space. Reconstructed eggs were compared fusion rates either at 2.0 ㎸/cm or 1.6 ㎸/cm(60 sec, double pulses). After fusion, all eggs were activated with the combination of 5 M ionomycin (5 min) and 10 g/$m\ell$ cycloheximide (CHX, 3h), and cultured in CRlaa medium and transferred into TCM199＋10% FBS on day 3. Although there was not significantly differ in fusion rate between treatments (60%, 2.0 ㎸/cm vs. 79.4%, 1.6 ㎸/cm), none of them in the eggs fused with 2.0 ㎸/cm developed to blastocyst. In comparison of development and chromosome status between different activation treatments (Group 1; 5 M ionomycin/10 g/$m\ell$ CHX, Group 2; 5 M ionomycin/5 g/$m\ell$ CHX ＋ 2 mM DMAP after fusion with 1.6 ㎸/cm), there were not differ in cleavage and development rates (67.3% and 28.9% in Group 1; 67% and 33% in Group 2). All out of 8 embryos evaluated in Group 1 appeared a normal diploid chromosome sets and mean number of cells (Mean SEM) on day 4.5 of culture was 141.5 23.15 (n=8). It can be concluded that the use of cycloheximide has not happened in chromosome abnormalities, and fetal fibroblasts can be used for cloning in rabbit.

• 농약과학회지
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• 제12권3호
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• pp.291-294
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• 2008

복숭아 미이라 과일로부터 복숭아 잿빛무늬병 Monilinia fructicola에 대하여 강한 항균활성을 보이는 방선균 Streptomyces padanus TH04를 분리하였다. TH04 균주의 배양 추출물 1%를 함유한 배지에서의 균사생육 및 포자발아는 시험한 M. fructicola의 strain에 따라 각각 $79.8{\sim}81%$와 $73.9{\sim}75.8%$ 억제되었다. 병원균과 TH04 균주 초기접종 밀도를 0.01%, 0.1% 및 1%로 달리하여 동시배양 한 결과, 항균활성은 선발 방선균의 밀도에 따라 $7.5%{\sim}94%$로 나타났다. 사과(품종; 후지)를 이용한 조추출물의 항균활성은 0.1% 처리구 85.9%, 1%처리구 100%로 나타났다. 항균활성 물질 생산, 안정성 및 제형화에 관한 연구가 이루어질 경우 선발한 Streptomyces padanus TH04는 생물학적 방제제로의 개발 가능성 있을 것으로 생각된다.

• Reproductive and Developmental Biology
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• 제30권1호
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• pp.47-52
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• 2006

본 연구는 단위발생유래 생쥐 배아줄기세포(P-mES)지가 체외수정유래 생쥐 배아줄기세포 (mES)와 마찬가지로 기능성 심근세포로 체외 분화되는지를 조사하였다. 각 세포주 P-mES04와 MES03를 4일간 부유 배양하여 배아체 (EB)를 형성한 다음 4일간 DMSO를 추가적으로 처리한 뒤 젤라틴이 코팅된 배양접시에 부착시켰다(4-/4+). P-mES04와 mES03으로부터 수축성 심근세포 생성 여부를 30일간 관찰한 결과, 각각 13일(69.83%)과 22일 (61.3%)에 누적 형성율이 가장 높았다. 면역 세포화학염색 결과, 수축성을 나타내는 P-mES04 세포는 수축성 mES03 세포에서와 같이 근육 특이적인 anti-sarcomeric a-actinin 항체와 심근 특이적인 anti-cardiac troponin I 항체에 염색되는 것을 확인하였다. 또한 RT-PCR 결과, 수축성을 나타내는 P-mES04 세포는 심근특이적인 L-type calcium channel, a1C, cardiac myosin heavy chain a, cardiac muscle heavy polypeptide $7{\beta}$, GATA binding protein 4와 atrial natriuretic factor는 발현하나, 골격근 특이적인 L-type calcium channel, a1S는 발현하지 않아 웅성 성체의 심장세포와 유사한 양상을 보였다. 본 연구의 결과는 단위발생 유래 생쥐 배아 줄기세포를 배아줄기세포의 연구의 대체제로 이용할 수 있음을 보여준다.

• 한국가축번식학회지
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• 제14권1호
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• pp.1-8
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• 1990

These experiments were carried out to investigate the effects of cumulus cells for in vitro fertilization and development of bovine follicular oocytes matured in vitro. The bovine ovaries were obtained at a slaughter house and the follicular oocytes surrounded by cumulus cells were collected by puncturing follicles with 2~6 mm of diameter. Bovine oocytes were matured in vitro for 24~26 hours in a CO2 incubator with 5% CO2 in air at 39$^{\circ}C$. The medium used for maturation was TCM-199 supplemented with hormones, pyruvate, FCS and antibiotics. Epididymal spermatozoa were capacitated by in vitro culture for 2~3 hours in BO solution containing BSA(5mg/ml) and caffeine(2.5mM). Insemination was made by introducing about 10~15 matured oocytes into the suspension of capacitated spermatozoa. Six hour after insemination the eggs were transferred to TCM-199 supplemented with FCS(10%) and HEPES(25mM), cultured for 7~8 days with 10~15 eggs/well in 4-well multidishes(Nunc Co.) forming cumulus cell monolayer. The results obtained in these experiments were summarized as follows ; 1. The majority of the follicular oocytes with compacted cumulus cells existed in GV stage while those with dispersed or denuded cumulus cells existed GVBD and M II stage. 2. After 24~26 hours maturation, the maturation rates of the follicular oocytes cultured in TCM-199 containing hormones were slightly higher than those of oocytes cultured in medium without hormones, and the frequency of cumulus compacted or denuded oocytes reaching M II stage cultured in medium containing hormones was 75.7% or 51.7%, respectively(P<0.05). 3. After 20 hours in vitro insemination, percentages of ova fertilized were 61.4% or 51.4%, respectively, for cumulus oophorus intacted or removed, and increased frequency of ova with both male and female pronuclei was found when cumuli were present(P<0.05). 4. The rates of embryos developed to 2-, 4-, 8-, 16-cell and morula or blastocyst stage after cocultured with cumulus cells were 65.0%, 45.3%, 34.7%, 28.0% and 22.7%, respectively. The results for momla or blastocyst stage were significantly higher than those of the embryos cultured in the basic medium(P<0.05).

• Journal of Plant Biotechnology
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• 제32권1호
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• pp.31-35
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• 2005

양파의 재분화 체계 확립을 위해 성숙된 양파의 종자로부터 성숙배를 적출한 후 2,4-D와 BA의 다양한 농도를 이용하여 체세포배발생 캘러스의 형성율을 조사하였다. 체세포 배발생 캘러스는 쉽게 부서지는 특성을 가지고 있었으며 비체세포배발생 캘러스는 물기를 많이 포함하고 있어 쉽게 구분이 가능하였다. 체세포배발생 캘러스는 picloram $2.5\;\cal{mg/L}$ 또는 $5\;\cal{mg/L}$가 단독으로 포함된 MS배지를 이용하여 $25^{\circ}C$ 암배양 4주 후 가장 높은 유도율을 나타내었다. 그러나 유도된 캘러스를 shoot로 재분화 시킨 결과 2,4-D와 BA $1\;\cal{mg/L}$가 혼합된 처리구에서 가장 높은 shoot 유기율을 나타내었다. 따라서 다른 처리에서 유도된 캘러스를 2,4-D와 BA $1\;\cal{mg/L}$가 포함된 액체배지에 현탁배양을 시도하였다. 현탁배양은 캘러스의 증가뿐만 아니라 캘러스의 cell cycle을 synchronized 함으로서 이후 형질전환이 용이할 것으로 판단되었다. 현탁 배양된 캘러스는 Kinetin $1\;\cal{mg/L}$가 포함된 1/2 MS 배지에서 60일간 광배양 하여 shoot 유기하였으며 유도된 shoot는 NAA $0.5\;\cal{mg/L}$가 포함된 발근배지에서 발근 후 순화하여 완전한 식물체로 재생할 수 있었다.

• 식물병연구
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• 제26권1호
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• pp.8-18
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• 2020

고추는 한국의 주요 경제 작물 중 하나이지만 재배과정에서 Colletotrichum acutatum에 기인한 탄저병이 많이 발생한다. 이의 방제를 위해 길항균인 Bacillus subtilis YGB36을 선발하여 16S rRNA 염기서열 및 생리·생화학적 분석을 통해 Bacillus subtilis로 동정하고 이를 생물학적 방제제로 개발하고자 실험을 진행하였다. In vitro screening에서 YGB36은 Cylindrocarpon destructans에 강한 항균활성을 나타내었고, cellulase, protease, amylase, siderophore 생산 및 phosphate solubility를 보유하고 있었다. 이 균주의 배양액(10⁶ cfu/ml) 및 배양여액은 in vitro 실험에서 C. acutatum의 포자발아를 강하게 억제하였고, 고추 과실을 이용한 실내실험에서도 이 배양액이 탄저병 병반의 진전을 억제하였으며, 방제가는 65.7%로 나타났다. 아울러 YGB36배양액은 고추 종자의 발아 및 초기 뿌리 생장을 촉진하였고, 온실에서의 식물 생장을 촉진하였다. 기존 화학농약과의 혼용 가능성 조사 결과, YGB36은 실험에 사용한 모든 살충제에서 생존에 영향을 전혀 받지 않았으며, 살균제 21종 중 11종에서 잘 생존하였다. 따라서 YGB36균주는 고추 탄저병에 대한 생물농약으로서의 잠재적 가치가 상당한 것으로 판단된다.

• Reproductive and Developmental Biology
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• 제36권1호
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• pp.33-37
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• 2012

Differential capacity of the parthenogenetic embryonic stem cells (PESCs) is still under controversy and the mechanisms of its neural induction are yet poorly understood. Here we demonstrated neural lineage induction of PESCs by addition of insulin-like growth factor-2 (Igf2), which is an important factor for embryo organ development and a paternally expressed imprinting gene. Murine PESCs were aggregated to embryoid bodies (EBs) by suspension culture under the leukemia inhibitory factor-free condition for 4 days. To test the effect of exogenous Igf2, 30 ng/ml of Igf2 was supplemented to EBs induction medium. Then neural induction was carried out with serum-free medium containing insulin, transferrin, selenium, and fibronectin complex (ITSFn) for 12 days. Normal murine embryonic stem cells derived from fertilized embryos (ESCs) were used as the control group. Neural potential of differentiated PESCs and ESCs were analyzed by immunofluorescent labeling and real-time PCR assay (Nestin, neural progenitor marker; Tuj1, neuronal cell marker; GFAP, glial cell marker). The differentiated cells from both ESC and PESC showed heterogeneous population of Nestin, Tuj1, and GFAP positive cells. In terms of the level of gene expression, PESC showed 4 times higher level of GFAP expression than ESCs. After exposure to Igf2, the expression level of GFAP decreased both in derivatives of PESCs and ESCs. Interestingly, the expression level of $Tuj1$ increased only in ESCs, not in PESCs. The results show that IGF2 is a positive effector for suppressing over-expressed glial differentiation during neural induction of PESCs and for promoting neuronal differentiation of ESCs, while exogenous Igf2 could not accelerate the neuronal differentiation of PESCs. Although exogenous Igf2 promotes neuronal differentiation of normal ESCs, expression of endogenous $Igf2$ may be critical for initiating neuronal differentiation of pluripotent stem cells. The findings may contribute to understanding of the relationship between imprinting mechanism and neural differentiation and its application to neural tissue repair in the future.

• Parasites, Hosts and Diseases
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• 제23권2호
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• pp.293-299
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• 1985

병원성 자유생활 아메바인 Naegleria fowleri를 CGVS 배지에서 무균적으로 배양하여 그 영향형을 복강내로 주입하여 인위적으로 면역시킨 마우스에 본 원충율 비강내로 감염시켰을때 방어면역이 생성되는지를 관찰하였다. 감염 8일후부터 마우스가 사망하기 시작하였고 이 마우스의 뇌에서 전형적인 원발성 아메바성 뇌수막염이 발생했음을 관찰할 수 있었다. N. fowleri 감염으로 인한 마우스의 사망율은 대조군에서 보다 네가지 항원으로 면역시킨 실험군에서 모두 현저히 낮았으며, 감염에서 사망할 때까지의 생존기간도 면역시킨 실험군에서 대조군보다 연장되었으나, N. fowleri 세포막항원으로 면역시킨 실험군에서는 대조군과 비교할때 차이가 없었다. 또한 N. gruberi 영양형으로 면역시킨 실험군에서도 생존기간이 연장되었다. 이상의 성적을 요약하면 N. fowleri를 마우스 복강내로 주입시켜 면역시킬 때 방어면역이 생성됨을 알 수 있었다.