• Asian-Australasian Journal of Animal Sciences
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• 제21권8호
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• pp.1127-1133
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• 2008

This study was designed to develop a method of liquid storage of boar sperm at $4^{\circ}C$ by using the modified Beltsville F5 (BF5) diluent with bovine serum albumin (BSA) and N-acetyl-D-glucosamine. Boar sperm were stored in lactose-egg yolk and N-acetyl-D-glucosamine (LEN), BF5 and Golden-Pig liquid 4 (GPL4) diluents at $4^{\circ}C$ for 5 days and were examined for sperm viability, adenosine triphosphate (ATP) and in vitro fertilization (IVF). The percentage of sperm viability in GPL4 diluent was higher than in LEN and BF5 diluent from 1 to 5 days of storage at $4^{\circ}C$. The percentage of sperm viability steadily declined from 1 to 5 days of storage in the three different diluents. Sperm ATP in GPL4 diluent was higher than in LEN and BF5 diluents from 1 to 5 days of storage. Sperm ATP rapidly declined after 5 days of storage in the three different diluents. Porcine oocytes matured in vitro were inseminated with different sperm concentrations of liquid semen stored for 3 days in GPL4 diluent. The percentage of monospermic oocytes did not show any differences from 2.5 to $20{\times}10^5$ sperm/ml. However, the percentage of polyspermic oocytes in the sperm concentration of $2.5{\times}10^5$ sperm/ml was lower than in concentrations of 5, 10 and $20{\times}10^5$5 sperm/ml. The percentage of blastocysts from the cleaved oocytes at $2.5{\times}10^5/ml$ sperm concentration was significantly lower than at 5, 10 and $20{\times}10^5sperm/ml$ concentrations. In conclusion, GPL4 diluent can be stored at $4^{\circ}C$ for 5 days and showed higher sperm viability and sperm ATP concentration compared with LEN and BF5 diluents. Also, we found that GPL4 diluent can be used for IVF of porcine oocytes.

• Maxillofacial Plastic and Reconstructive Surgery
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• 제33권5호
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• pp.385-391
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• 2011

Purpose: The periosteum is a well-known source of osteogenic precursor cells for tissue-engineered bone formation. However, cultured endothelial or endothelial-like cells derived from periosteum have not yet been investigated. This study focused on endothelial-like cell culture from the periosteum. Methods: Periosteal tissues were harvested from the mandible during surgical extraction of lower impacted third molars. The tissues were treated with 0.075% type I collagenase in phosphate-buffered saline (PBS) for 1 hr at $37^{\circ}C$ to release cellular fractions. The collagenase was inactivated with an equal volume of DMEM/10% fetal bovine serum (FBS) and the infranatant was centrifuged for 10 min at 2,400 rpm. The cellular pellet was filtered through a $100{\mu}m$ nylon cell strainer, and the filtered cells were centrifuged for 10 min at 2,400 rpm. The resuspended cells were plated into T25 flasks and cultured in endothelial cell basal medium (EBM)-2. Results: Among the hematopoietic markers, CD146 was more highly expressed than CD31 and CD34. The periosteal-derived cells also expressed CD90 and CD166, mesenchymal stem cell markers. Considering that the expression of CD146 was constant and that the expression of CD90 was lower at passage 5, respectively, the CD146 positive cells in passage 5 were isolated using the magnetic cell sorting (MACS) system. These CD146 sorted, periosteal-derived cells formed tube-like structures on Matrigel. The uptake of acetylated, low-density lipoprotein, labeled with 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (DiI-Ac-LDL) was also examined in these cells. Conclusion: These results suggest that the CD146-sorted positive cells can be referred to as periosteal-derived CD146 positive endothelial-like cells. In particular, when a co-culture system with endothelial and osteoblastic cells in a three-dimensional scaffold is used, the use of periosteum as a single cell source would be strongly beneficial for bone tissue engineering.

• 한국음향학회지
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• 제39권1호
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• pp.16-23
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• 2020

고강도 집중 초음파(High-Intensity Focused Ultrasound, HIFU) 치료에서 HIFU 초점의 효과적인 위치 파악은 안전한 치료 계획을 개발하는 데 중요하다. 자기 공명 영상 유도 HIFU(Magnetic Resonance Imaging guided HIFU, MRIgHIFU)는 HIFU 초점을 영상화하여 치료 중에 초음파 경로를 시각화 할 수 있지만 초음파 이미징 유도 HIFU(Ultrasound imaging guided HIFU, USIgHIFU)에서는 어려움이 있다. 본 연구에서는 USIgHIFU에 대해 HIFU 초점을 영상화할 수 있는 실시간 초음파 빔 시각화 기법을 제시 하였다. 제안 된 방법에서, 음향 강도(Ispta < 720 mW/㎠) 아래의 이미징 초음파 변환자의 동일한 중심 주파수를 갖는 짧은 펄스가 HIFU 변환기를 통해 전송되고, HIFU 빔 경로를 시각화하기 위해 수신 신호는 동적 수신 포커싱 및 후속 에코 처리를 거쳤다. 소 혈청 알부민 젤 팬텀을 이용한 생체외 실험으로부터, HIFU 빔 경로는 낮은 음향 강도 (Ispta = 94.8 mW/㎠)에서도 명확히 영상화 할 수 있었고 HIFU 초점은 손상이 생성되기 전에 성공적으로 시각화하였다. 이 결과는 제안 된 초음파 빔 경로 시각화 방법이 USIgHIFU 치료에서 원치 않는 조직 손상을 최소화하면서 실시간으로 HIFU 초점을 영상화하는 데 사용될 수 있음을 나타낸다.

• 한국환경보건학회지
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• 제42권4호
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• pp.266-273
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• 2016

Objectives: This study evaluated the virucidal efficacy against avian influenza virus (AIV) of a disinfectant spray containing 0.25% grapefruit seed extract, 0.2% citric acid, 0.0625% malic acid and 0.0125% benzalkonium chloride. Methods: The disinfectant spray was diluted several times with hard water (HW) and organic matter (OM). Two point five mL of each diluent was added into each test tube, and 2.5 mL of AIV suspension was inserted into each test tube. After 30 minutes of virus-disinfectant contact reaction at $4^{\circ}C$, 2.5 mL of 10% inactivated fetal bovine serum was added into each test tube to neutralize the sanitizer efficacy. The neutralized solutions were serial 10-fold dilutions with phosphate buffer solution, and 0.2 mL of the diluents was injected into the allantoic cavity of five ten-day-old-chickens per dilution time. After incubation of the embryos for five days, the viability of the AIV was examined by hemagglutination titer. The valid dilution of the disinfectant spray was estimated according to the dilution time that the virus titer was inactivated more than $10^4$ 50% egg-infective dose (EID50)/mL compared with pathogen control. Results: In HW and OM conditions, the valid dilutions of the disinfectant spray against AIV were seven- and three-fold dilutions, respectively. The AIV titer of the pathogen control was more than 6.1 log10EID50/mL, and there was no embryonic toxicity. Conclusion: The present study showed that this disinfectant spray has effective virucidal activity against AIV.

• Asian-Australasian Journal of Animal Sciences
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• 제29권3호
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• pp.343-351
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• 2016

Although the chemical, physical, and nutritional properties of bovine milk have been extensively studied, only a few studies have attempted to characterize milk-synthesizing genes using RNA-seq data. RNA-seq data was collected from 21 Holstein samples, along with group information about milk production ability; milk yield; and protein, fat, and solid contents. Meta-analysis was employed in order to generally characterize genes related to milk production. In addition, we attempted to investigate the relationship between milk related traits, parity, and lactation period. We observed that milk fat is highly correlated with lactation period; this result indicates that this effect should be considered in the model in order to accurately detect milk production related genes. By employing our developed model, 271 genes were significantly (false discovery rate [FDR] adjusted p-value<0.1) detected as milk production related differentially expressed genes. Of these genes, five (albumin, nitric oxide synthase 3, RNA-binding region (RNP1, RRM) containing 3, secreted and transmembrane 1, and serine palmitoyltransferase, small subunit B) were technically validated using quantitative real-time polymerase chain reaction (qRT-PCR) in order to check the accuracy of RNA-seq analysis. Finally, 83 gene ontology biological processes including several blood vessel and mammary gland development related terms, were significantly detected using DAVID gene-set enrichment analysis. From these results, we observed that detected milk production related genes are highly enriched in the circulation system process and mammary gland related biological functions. In addition, we observed that detected genes including caveolin 1, mammary serum amyloid A3.2, lingual antimicrobial peptide, cathelicidin 4 (CATHL4), cathelicidin 6 (CATHL6) have been reported in other species as milk production related gene. For this reason, we concluded that our detected 271 genes would be strong candidates for determining milk production.

• 대한치과교정학회지
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• 제24권1호
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• pp.17-35
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• 1994

Vanadium is an essential trace element but has not been identified with a specific biogical role. To study the direct effects of vanadium on osteoblast, we incubated murin osteoblast-like (MC3T3-El) cells with various corcentration of vanadium oxide & sodium orthovanadate. This study was designed to investigate the effect of vanadium on DNA synthesis, alkaline phosphatase (ALP) activity, cAMP formation responsive to parathormone(PTH) and type I $\alpha$ 2 collagen ribonucleic acid (mRNA) level in murin osteoblast-like (MC3T3-El) cells. The cells were cultured in $\alpha-minimal$ essential medium$(\alpha-MEM)$ supplemented with $10\%$ fetal bovine serum (FBS) and then changed to $0.1\%$ FBS with various concenoation of vanadium oxide & sodium orthovanadate. Quiescent cultured MC3T3-El cells incubated for 24 hours with 2,5,10,15,20 ${\mu}M$ vanadium oxide incorporated $[^3H]Thymidine;$ every concentration showed increases in $[^3H]Thymidine$ incorporations dose dependant manner, the greatest response occurred at $20{\mu}M$. Quiescent cultured MC3T3-E1 cells incubated for 3days with 2,5,10,15,20 ${\mu}M$ vanadium oxide, for 2days with sodium orthovanadate and alkaline phosphatase was assayed with disodium phenyl phosphate as substrate. Vanadium oxide increased the alkaline phosphatase content in MC3T3-El cells at $2{\mu}M\;&\;6{\mu}M$ ; the greatest response occurred at $2{\mu}M$. But decreased at other content sodium orthovanadate increased alkaline phosphatase content in MC3T3-El cells at all concenoation ; the greatest response occurred at $4{\mu}M$. Quiescent cultured MC3T3-El cells incubated for 3days with $5,10{\mu}M$ vanadium oxide , with $5,8{\mu}M$ sodium orthovanadate and cAMP formation was measured by Radioimmunoassay(RIA). Vanadium oxide & sodium orthovanadate showed the tendency of inhibitory effects on cAMP responsiveness to PTH in MC3T3-El cells. Quiescent cultured MC3T3-El cells incubated for 24hours with $10,20{\mu}M$ vanadium oxide, with $5,10{\mu}M$ sodium orthovanadate and Type I $\alpha$ 2 collagen ribonucleic acid (mRNA) expression was studied by Nothern blot analysis. Northern blot analysis of vanadium oxide treated cells showed decreasing effects 0& sodium orthovanadate revealed increasing effects in type I $\alpha$ 2 collagen ribonucleic acid (mRNA) level.

• 한국식품영양과학회지
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• 제32권4호
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• pp.586-590
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• 2003

사람 간 배양세포 유래 HePG2 세포에 영양성분을 이용하여 실험적으로 중성지질을 축적시킨 상태에서 한방 황련해독탕(HT)의 약리적 효과를 검토하였다. 간세포는 1 mM oleate, 0.2% BSA, glucose 4.5 mg/mL 및 HT 무첨가(대조구) 또는 첨가한(0.5 mg/mL 및 5.0 mg/mL) DME배지에서 6시간 및 24시간 배양하였으며(실험 I), 이때 황련해독탕을 첨가한 배양액에는 ［$^{14}$ C］-oleate (0.5 $\mu$Ci/mL medium)를 동시에 첨가하여 중성지질 획분에의 동위원소 추적실험을 하였다. 또한, 간세포에 2 mM oleate, 0.5% BSA, glucose 4.2mg/mL 및 HT 무첨가(대조구) 또는 첨가한(0.5 mg/mL 및 5.0 mg/mL) DME배지에서 6, 24및 48시간 배양(실험 II) 또는 1 및 3시간 배양(실험 III)하였다. 실험 I에서 세포내 중성지질 농도는 HT첨가 6 및 24시간 배양에서 약물농도첨가 의존적으로 감소하였다. 이때 HT첨가시 ［$^{14}$ C］-oleate 동위원소는 세포내 중성지질 획분의 추적량과 세포외 분비량이 현저하게 감소하였다. 실험 I조건에 비해 고농도의 영양성분을 첨가시킨 실험 II 및 III 조건에서 세포내 중성지질 축적이 확인되었으며, 이 때 HT 첨가 24 및 48시간 배양에서는 세포내 중성지질 축적이 현저히 억제되는 것으로 나타났다. 이상의 결과에서, 본 실험에 사용된 한방 황련해독탕은 사람 간배 양 HePG2 세포내 중성 지질 합성을 저하시켜 중성지질 축적을 억제시킴으로써 지방간 개선효과를 발휘한 것으로 시사되었다.

• Imaging Science in Dentistry
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• 제35권3호
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• pp.127-131
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• 2005

Purpose : We performed the present study to investigate whether osteotropic hormomes play roles on the nitric oxide (NO) production in culture of ROS 17/12.8 osteoblastic cells. Materials and Methods : The osteoblastic cell line ROS17/2.8 cells were cultured In F12 medium supplemented with $5\%$ fetal bovine serum (FBS) at $37^{\circ}C$ in a humidified atmosphere of $5\%\;CO_2$ in air. ROS17/2.8 cells were plated in 96-well plates at a density of $2-3\times10^3cells/well$ and grown to confluence. Then the cells were pretreated with osteotropic hormones (parathyroid hormone (PTH) 20-500 ng/mL, 1, 25-dihydroxycholecalciferol $(1,\;25[OH]_2D_3)$ 1-100 nM; prostaglandin $E_2 (PGE_2)$ 20-500 ng/mL in the medium supplemented with $0.4\%$ FBS for 72 hours and the cells were treated with cytokines $(TNF{\alpha}\;and\;IFN{\gamma})$ in phenol red-free F12 medium for an additional 48 hours. NO synthesis was assessed by measuring the nitrite anion concentration, the reaction product of NO, in the cell culture medium using Griess reagent. Results : PTH and $1,\;25[OH]_2D_3$ pretreatment induced a significant increase in NO production in the presence of $TNF{\alpha}\;and\;IFN{\gamma}.\;PGE_2$ slightly induced NO production compared to the control group. But, $PGE_2$ pretreatment did not affect in NO production in the presence of $TNF{\alpha}\;and\;IFN{\gamma}$. Conclusions : These results suggest that the actions of osteotropic hormones In bone metabolism may be partially mediated by NO in the presence of cytokines.

• KSBB Journal
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• 제16권1호
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• pp.48-53
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• 2001

상 접촉법을 이용하여 BSA를 음이온 계면활성제인 AOT와 isooctane으로 구성된 역미셀상으로 가용화하였다. 본 연구에서는 pH와 염의 종류 및 농도가 가용화 효율에 미치는 영향에 주목하였다. 0.1 M의 KCl, NaCl, $MgCl_2$, 그리고 $CaCl_2$와 같이 1:1 염 혹은 1:2 염을 수용액에 첨가하면 첨가한 염의 종류에 따라 pH=5~7사이에서 최대의 가용화 효율을 보였다. $CaCl_2$와 NaCl의 경우, 1 M 까지는 첨가한 염의 농도가 증가함에 따라 효율도 증가하였으나 $MgCl_2$의 경우에는 특이한 경향을 보였다. 염의 농도가 낮거나 pH가 낮은 경우에는 단백질이 광범위하게 수용액상과 유기상의 계면에서 침전되는 것은 주목할 부분이다. 역미셀의 water-pool 크기는 물에 대한 계면활성제의 몰비인 $W_0$를 측정하여 추산하였다. $MgCl_2$의 경우에는 pH변화에 관계없이 $W_0$=20의 거의 일정한 값을 보인 반면 $CaCl_2$와 KCl의 경우 염 농도가 증가함에 따라 $W_0$는 감소하였다.

• 한국발생생물학회지:발생과생식
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• 제17권3호
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• pp.269-274
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• 2013

This study was performed to evaluate the effects of fibroblast co-culture on in vitro maturation (IVM) of prepubertal mouse preantral follicles. The intact preantral follicles were obtained from the ovaries of 12-14 day old mice and these were cultured individually in ${\alpha}$-minimal essential medium (${\alpha}$-MEM) supplemented with 5% fetal bovine serum (FBS), $100mIU/m{\ell}$ recombinant follicle stimulating hormone (rFSH), 1% insulin-transferrin-selenium, $100{\mu}g/ml$ penicillin and $50{\mu}g/m{\ell}$ streptomycin as base medium for 12 days. A total of 200 follicles were cultured in base medium co-cultured with mouse embryonic fibroblast (MEF) (MEF group) (n=100) or only base medium as control group (n=100). Survival rate of follicles on day 12 of culture were significantly higher in the MEF group of 90.0%, compared with 77.0% of the control group (p=0.021). Follicle diameters on day 6 and 8 of the culture period were significantly larger in the MEF group than those in the control group (p=0.021, p=0.007, respectively). Estradiol levels in culture media on day 4, 6, 8, 10 and 12 of the culture period were significantly higher in the MEF group (p=0.043, p=0.021, p=0.006, p<0.001 and p=0.008, retrospectively). Our data suggest that MEF cell co-culture on IVM of mouse preantral follicle increases survival rate and promotes follicular growth and steroid production.