• Journal of Plant Biotechnology
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• 제30권3호
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• pp.257-261
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• 2003

This experiment was carried out to investigate the effects of plant growth regulators on the organogenesis from the tissue culture of Arabidopsis thaliana stem, and the origin of the callus development. When the stem segments were cultured on medium with 2mg/L IAA or NAA, adventitious roots and trichomes were differentiated after 11 days of culture. Callus vigorously formed on medium with 2/L2,4 after 7 days of culture, but adventitious roots and trichomes were not differentiated from callus after 10 days of culture. This results suggesting that picloram is very effective auxin for the callus formation and organogenesis. Callus weakly formed on 0.05mg/L kinetin, and formed on combination of auxins(2mg/L) with 0.05mg/L kinetin. But the effect of combination of auxins and kinetin the callus formation was less than 2,4-D or picloram alone. A histological examination of callus formed on picloram showed that phloram showed that phloem parenchyma cells were divided and enlarged after 2 days of culture. Cortex parenchyma cells were divided and meristematic nodules were developed from these cells after 4 days of culture. Finally, callus formed on outside of cortex and epidermis by division of meristematic nodules after 7 days of culture.

• 대한화장품학회지
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• 제31권1호
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• pp.97-102
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• 2005

수분 보유력이 우수한 hyaluronan (HA)은 피부 보습에 관여하는 여러 물질들 중 하나로 피부의 extracellular matrix를 구성하는 주요 성분 중 하나이다. Glycosaminoglycans (GAGs)의 구성 성분의 하나로 과거에는 진피에서 유래하는 것으로 알려져 왔으나 최근 연구들을 통해 표피에서 합성되는 것이 확인되었다. Polyphenolic compound의 일종인 kaempferol과 quercetin은 채소류 같은 식물성 음식에 많이 존재하는 것으로 알려져 있으며, kaempferol은 인체 표피세포에서 glutathione 합성을 증가시키고 quercetin은 lipoxygenase inhibitor로 PPAR (peroxisome proliferator activated receptor) - mediated 표피세포 분화를 억제하는 것으로 알려져 있다. 본 연구에서 우리는 표피 세포주에서 이들 flavonoids -kaempferol, quercetin -의 HA 합성에 미치는 영향을 알아보고자 하였다. 물질 처리에 따른 HA 합성 효소인 hyaluronan synthase 1, 2, 3 (HAS1, 2, 3) 유전자 발현의 변화를 semi-quantitative RT-PCR을 통해 살펴보았다. 이들 flavonoid들에 의해 24 h 후 HAS2, 3 mRNA 발현이 증가되는 것을 발견하였다. 또한 HA 합성량의 변화를 알아보기 위해 ELISA를 수행하였다. 24 h 물질 처리 후 배지를 수거하여 HA 합성량을 살펴본 결과 이들 물질에 의해 합성이 유의하게 증가함을 알 수 있었다. 비록 합성 촉진에서의 효과가 retinoic acid에는 못 미치지만 kaempferol과 quercetin은 표피 세포주에서 농도 의존적으로 HA 합성을 증가시켰다. 위의 결과를 통해 flavonoid류인 kaempferol과 quercetin이 피부에서 HA 생산을 촉진시킴을 알 수 있었고 이를 통해 피부 보습과 잔주름 개선에 효과를 볼 수 있을 것으로 생각된다.

• Journal of Microbiology and Biotechnology
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• 제32권2호
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• pp.238-247
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• 2022

Since the skin covers most surfaces of the body, it is susceptible to damage, which can be fatal depending on the degree of injury to the skin because it defends against external attack and protects internal structures. Various types of artificial skin are being studied for transplantation to repair damaged skin, and recently, the production of replaceable skin using three-dimensional (3D) bioprinting technology has also been investigated. In this study, skin tissue was produced using a 3D bioprinter with human skin cell lines and cells extracted from mouse skin, and the printing conditions were optimized. Gelatin was used as a bioink, and fibrinogen and alginate were used for tissue hardening after printing. Printed skin tissue maintained a survival rate of 90% or more when cultured for 14 days. Culture conditions were established using 8 mM calcium chloride treatment and the skin tissue was exposed to air to optimize epidermal cell differentiation. The skin tissue was cultured for 14 days after differentiation induction by this optimized culture method, and immunofluorescent staining was performed using epidermal cell differentiation markers to investigate whether the epidermal cells had differentiated. After differentiation, loricrin, which is normally found in terminally differentiated epidermal cells, was observed in the cells at the tip of the epidermal layer, and cytokeratin 14 was expressed in the lower cells of the epidermis layer. Collectively, this study may provide optimized conditions for bioprinting and keratinization for three-dimensional skin production.

• Journal of the Korean Association of Oral and Maxillofacial Surgeons
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• 제31권2호
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• pp.143-149
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• 2005

Objects : With the advancement of tissue engineering techniques, the effort to develop bioartificial mucosa have been actively delivered. The problem we met with this technique is the lack of mechanical strength between kerationocyte layer and dermal layer, where in the normal skin and mucosa, they are tightly bound with rete ridge structure. The purpose of this study is to understand the 2D and 3D structure of rete ridge of mucosa and skin paddle for rendering more biomimetic structure to the artificial mucosa. Materials and Methods : Oral mucosa and skin from the patients who received the oral surgery and maxillofacial reconstruction were harvested. The epidermis was separated from the dermis after treating with dispase for 12-16 hours. H&E staining was performed for 2D(dimensional) structure study and confocal LASER and SEM study were performed for 3D structure. Mean height(Sc) and arithmetic mean deviation(Sa) of all surface height were calculated. Results : The average height of rete ridge of skin flap was between $67.14{\mu}m$ and $194.55{\mu}m$. That of oral mucosa was between $146.26{\mu}m$ and $167.51{\mu}m$. Pressure bearing area and attached gingiva of oral mucosa showed deeper rete ridges. Conclusion : To obtain the adequate strength of artificially cultured keratinocyte skin and mucosa flap, it is necessary to imitate the original skin and mucosa structure, especially rete ridge. Through this study, 2D and 3D rete ridge structure of normal mucosa and skin was obtained. These results can be used as basis for substrate morphology for keratinocytes culture.

• 식물조직배양학회지
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• 제26권3호
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• pp.197-203
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• 1999

수분후 담배의 배에 중이온 beam ($^{14}$ N)을 조사하여 얻은 종자로부터 albino식물체를 분리하여 기내 생장과 분화의 특성을 검토하였다. 기내에서 생장시킨 albino식물체는 엽록소함량이 급격한 감소를 나타내었고 기공수는 잎의 이면 및 표면 표피에서 녹색 식물체 보다 많았다 연속광 조건하의 탄소원을 첨가한 MS배지에서 albino개체는 절간이 신장하지 않았으나 10.0mg/L 의 GA$_3$처리로 절간신장이 회복되었다. 잎절편 배양시 albino식물체는 1.0 mg/L 의 BAP와 kinetin의 단용처리로 다수의 신초를 형성하였고, 1.0mg/L의 2,4-D와 NAA의 단용처리로 다량의 캘러스를 형성하였다. 잎절편에서 유도된 albino 캘러스에 1.0mg/L BAP+0.1mg/L NAA를 혼용처리하면 다수의 식물체가 재분화 되었다. 이와같이 albino 식물체는 다경줄기 형성, 캘러스 형성, 캘러스로부터 재분화율 등이 녹색 식물체와 차이가 없었다. 또한 NAA와 BAP를 혼용처리 하였을 때 잎절편으로부터 기관분화의 유형도 정상주와 비슷하였다. 이러한 결과는 본 albino담배 변이체가 색소체 함량의 급감과 같은 광합성과 관련된 기능에서는 결손을 보이고 있음에도 불구하고 조직수준의 기관분화계에는 이상이 없다는 것을 시사한다.