• 제목/요약/키워드: tissue cultures

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캐드캠 기능을 이용한 전치부 심미 수복 및 전치부 임플란트에서 지르코니아 링크 지대주(Hybrid abutment)의 사용 (The use of zirconia hybrid abutment for the anterior esthetic restoration and anterior implant utilizing CAD/CAM technology)

  • 김종엽
    • 대한심미치과학회지
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    • 제22권1호
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    • pp.9-21
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    • 2013
  • 심미의 기준은 시대와 문화 그리고 개개인의 주관적인 관점에 따라 각기 다를 수 있다. 하지만 심미적인 부위를 수복하는 치과의사로서 일반적으로 따라야 할 원칙과 기준들이 있으며 수복물의 형태와 주변치아와의 조화 등을 위해 캐드캠의 몇몇 기능들은 아주 유용한 것으로 보이며, 전통적인 작업 방식에 비해 효율성도 높은 것으로 보인다. 또한 전치부 임플란트에서 치은이 얇은 경우 기계적인 문제를 줄이면서도 지르코니아 등의 도재를 사용하기 위한 한 방법인 링크 지대주에 대해 함께 알아보려 한다.

Role of phospholipase D and osteopontin in reactive glial cells after transient forebrain ischemia

  • Kim, Seong-Yun
    • 한국응용약물학회:학술대회논문집
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    • 한국응용약물학회 2000년도 춘계학술대회
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    • pp.15-16
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    • 2000
  • Transient forebrain ischemia results in delayed neuronal death in the CA1 region of the hippocampus after injury, which is, at least in part, a consequence of excessive generation of reactive oxygen species. Previous in vitro studies using cell cultures or brain slices have demonstrated that phospholipase D (PLD) in the nervous system is involved in the signaling mechanism in response to a variety of agonists. Several recent studies have shown that reactive oxygen species stimulate phospholipase D (PLD) activity in several kinds of cells. Therefore, this raises the possibility that PLD activity is enhanced in the ischemic brain. Meanwhile, osteopontin (OPN) was initially identified as a sialoglycoprotein in bone, but has since been found in various tissues. Although not much is known about its function, OPN seems to play an important role in inflammation and tissue repair. Recently, it was reported that OPN was upregulated in the activated microglia after focal brain ischemia, suggesting that OPN might play a role in wound healing after a focal stroke.

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작약의 미세번식에서 배지성분이 배양의 변색과 괴사에 미치는 영향 (Effects of Medium Components on Discoloration an Necrosis of Cultures in Peony (Paeonia lactiflora Pall.) Micropropagation)

  • 최상진
    • 식물조직배양학회지
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    • 제21권3호
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    • pp.173-176
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    • 1994
  • 작약절편을 접종하면 배지와 절편이 흑갈색으로 변하고 수 이로부터 배양이 죽기 시작하는데 배지성분 중에 이를 조장하는 물질이 있음을 발견하였다. 즉 변색의 주원인은 철분과 염화칼슘(Cacl$_2$)이었고, 절편을 괴사시키는데 가장 큰 영양을 미친 것은 NO$_3$었다. 이 결과를 토대로 피해가 비교적 적은 1/4 MS를 번식용 배지로 이용하여 식물체의 모든 부분을 배양하였을 때 조직으로부터 재생은 전혀 일어나지 않았다. 다만 줄기절편에서 이미 형성된 액아가 유식물체로 성장하기도 하였으나 건전한 것으로 계속 성장하지 못하였으며 이것을 다시 번식체로 이용할 때는 초기 배양의 절편에서 나타나는 현상과 같은 원인으로 인하여 생존하지 못하였다.

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Engineering of a Human Skin Equivalent

  • Ghalbzouri Abdoelwaheb El
    • 대한화장품학회지
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    • 제29권2호
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    • pp.105-130
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    • 2003
  • Human skin equivalents, also designated as cultured skin substitute (Boyce and Warden, 2002) or organotypic co-cultures (Maas-Szabowski et al., 1999, 2000, 2003), are three-dimensional systems that are engineered by seeding fibroblasts into a three-dimensional dermal matrix. Such a dermal equivalent is then subsequently seeded with human keratinocytes. After cell attachment, the culture is kept first under submerged condition to allow keratinocyte proliferation. Thereafter, the culture is lifted the air-liquid interface (A/L) to expose the epidermal compartment to the air, and to further induce keratinocyte differentiation. During the air-exposure, nutrients from the medium will diffuse through the underlying dermal substrate towards the epidermal compartment and support keratinocyte proliferation and differentiation. Under these conditions, a HSE is formed that shows high similarity with the native tissue from which it was derived (Figure 1) (Bell et at., 1981; Boyce et al., 1988; Ponec et al., 1997;El Ghalbzouri et al.., 2002).

In Vitro Morphogenesis through Leaf Explants of Gypsophila paniculata L.

  • Jo, Man-Hyun;Ham, In-Ki;Song, Nam-Hyun
    • Plant Resources
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    • 제3권2호
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    • pp.135-137
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    • 2000
  • Callus cultures from leaf explants of Gypsophila paniculata L. cv. 'Bristol Fairy' have been tested their growth and morphogenic capacity on Murashige and Skoog medium supplemented with 0.l, 0.5, 1 and 3 mg/L 2,4-D. The frequency of callus formation ranged from 43.3% to 100%. The optimal 2,4-D concentration for promoting callus formation and growth was 0.5 to 3 ㎎/L. 4.2∼ 5.6% of adventitious roots were obtained with the use of 0.1 and 0.5 mg/L 2,4-D. Calli grown well on 1.0 mg/L 2,4-D was the heaviest among the calli grown in various concentrations.

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The effect of mushroom components on the proliferation of HeLa cell line in vitro

  • Chung, Kyu-Sun
    • Archives of Pharmacal Research
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    • 제2권1호
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    • pp.25-33
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    • 1979
  • In order to find out nutritional effects of Korean edible mushrooms on the multiplication of tissue cells, the alcohol extracts and acid bydrolysates of eleven species of mushrooms were added to Earle's ESS. A comparison of the respective multiplications of HeLa cells in this solution and in control solution of TC=199. Yielded the following result: The alcohol extracts and acid hydrolysates of a Coprinus comatur, Agaricus campestris, Agaricus bisporus, Lentinus edodes, Tricholoma matsutake, Pleurotus ostretus, Ramaria botrytis and Pholiota nameko influenced favorably the maintenance of the normal form and monolayer of HeLa cells. The growth curves of HeLa cells in the cultures containing, respectively, the alcohol extracts and acid hydrolysates of these eight mushrooms showed that five species, i.e., Coprinus comatus, Agaricus compestris, Agaricus bisporus, Lentinus edodes and Tricholoma matsutake effected an excellent multiplication and that the other three species were less effective than those five species. As to the effects on the cell multiplication, no marked difference was observed between the alcohol extracts and the acid hydrolysates of the mushrooms tested.

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Somatic embryogenesis and plant regeneration in zygotic embryo explant cultures of rugosa rose

  • Kim, Suk Weon;Oh, Myung Jin;Liu, Jang R.
    • Plant Biotechnology Reports
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    • 제3권3호
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    • pp.199-203
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    • 2009
  • Rugosa rose (Rosa rugosa) is cultivated as a garden flower and an important genetic resource for the breeding of roses (R. hybrida). This study describes culture conditions for high frequency plant regeneration from zygotic embryo explants via somatic embryogenesis in rugosa rose. Mature zygotic embryo, cotyledon, and radicle explants formed embryogenic calluses at frequencies of 38, 6.7, and 8.8% when cultured on half-strength Murashige and Skoog medium (${\frac{1}{2}}MS$) supplemented with 2.26, 9.05, and $9.05{\mu}M$ 2,4-dichlorophenoxyacetic acid, respectively. Embryogenic calluses produced numerous somatic embryos, which then developed into plantlets on ${\frac{1}{2}}MS$ without growth regulators. Regenerated plantlets were grown to whole plants in a growth chamber.

PRODUCTION OF GINSENOSIDES THROUGH IN VITRO CULTURE OF GINSENG(Panax ginseng C.A. MEYER)

  • Choi K.T.;Ahn I.O.;Park J.C.
    • 고려인삼학회:학술대회논문집
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    • 고려인삼학회 1993년도 학술대회지
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    • pp.143-149
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    • 1993
  • Ginseng root explants and calli induced from selected cell lines were cultured on modified Murashige and Skoog's media supplemented with different concentrations of organic or inorganic compounds and plant growth requlators to clarify the effects of chemical composition and plant growth regulators in the medium on the growth of ginseng calli and the production of ginseng saponin. For optimum growth of calli, the concentrations of 2, 4-D and sucrose were the range of 1 to 3 mg/${\ell}$l and 1 to $3\%,$ respectively. And it was clarified that sucrose, nitrogen, phosphate, calcium, magmesian plant growth regulators and their concentrations influcenced the relative biosynthesis of saponin in tissue cultures of Panax ginseng. The patterns of ginsenosides, pharmacologically useful component, were different among the cell lines and contents of ginsenosides were much higher in selected cell lines than in original cell line.

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Neural Organoids, a Versatile Model for Neuroscience

  • Lee, Ju-Hyun;Sun, Woong
    • Molecules and Cells
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    • 제45권2호
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    • pp.53-64
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    • 2022
  • Three-dimensional cultures of human neural tissue/organlike structures in vitro can be achieved by mimicking the developmental processes occurring in vivo. Rapid progress in the field of neural organoids has fueled the hope (and hype) for improved understanding of brain development and functions, modeling of neural diseases, discovery of new drugs, and supply of surrogate sources of transplantation. In this short review, we summarize the state-of-the-art applications of this fascinating tool in various research fields and discuss the reality of the technique hoping that the current limitations will soon be overcome by the efforts of ingenious researchers.

Guidelines for Manufacturing and Application of Organoids: Brain

  • Taehwan Kwak;Si-Hyung Park;Siyoung Lee;Yujeong Shin;Ki-Jun Yoon;Seung-Woo Cho;Jong-Chan Park;Seung-Ho Yang;Heeyeong Cho;Heh-In Im;Sun-Ju Ahn;Woong Sun;Ji Hun Yang
    • International Journal of Stem Cells
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    • 제17권2호
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    • pp.158-181
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    • 2024
  • This study offers a comprehensive overview of brain organoids for researchers. It combines expert opinions with technical summaries on organoid definitions, characteristics, culture methods, and quality control. This approach aims to enhance the utilization of brain organoids in research. Brain organoids, as three-dimensional human cell models mimicking the nervous system, hold immense promise for studying the human brain. They offer advantages over traditional methods, replicating anatomical structures, physiological features, and complex neuronal networks. Additionally, brain organoids can model nervous system development and interactions between cell types and the microenvironment. By providing a foundation for utilizing the most human-relevant tissue models, this work empowers researchers to overcome limitations of two-dimensional cultures and conduct advanced disease modeling research.