• 식물조직배양학회지
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• 제28권1호
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• pp.1-6
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• 2001

카사바 (Manihot esculenta Crantz, cv. MCol 22)의 마디 및 절간절편으로부터 부정근 발생이 분화결정되는 시기를 조사하였다. 1개의 액아를 가진 10mm 길이의 마디절편을 MS 기본배지에서 8일간 배양하면 직접 부정근이 발생되었으나, 액아를 갖지 아니한 절간절편은 동일한 배지상에서 부정근이 형성되지 않았다. 반면에 마디절편을 MS 기본배지에서 5일간 배양한 뒤, 마디절편의 중간부로부터 절단된 하부의 절간절편으로부터는 부정근이 발생되었다. 이에 따라 마디절편의 중간 부를 일정시간 단위로 절단하는 방법으로 조사된 분화결정 시기는 3∼5일이었다. 한편 절간절편을 여러가지 농도의 IBA가 첨가된 배지에서 일정 기간 배양한 후 MS 기본배지로 이식했을 때 부정근이 발생되는 시기는 옥신 농도와 배양기간 에 따라 달랐다. 0.5 mg/L IBA 첨가에서는 5일 이상 배양되어야 90% 이상의 절편에서 부정근이 발생되고, 1 mg/L IBA 첨가에서는 2.5일 이상 처리에서, 그리고 2mg/L IBA에서는 1.5일의 처리에서 90% 이상의 부정근이 발생되었다. 따라서 부정근 발생을 분화결정시킨 외래 옥신의 처리기간은 분화결정 시기이라기보다는 근원기 유도에 필요한 적정량의 옥신을 흡수축적한 기간으로 사료된다.

• Journal of Plant Biotechnology
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• 제47권1호
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• pp.53-65
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• 2020

Here, we describe an efficient and rapid protocol for the micropropagation of Thymus pallidus Cosson ex Batt., a very rare medicinal and aromatic plant in Morocco. After seed germination, we tested the effect of different macronutrients, cytokinins alone or in combination with gibberellic acid (GA₃) or auxins, on T. pallidus plantlet growth. We found that Margara macronutrients (N₃₀K) had the best effect on the in vitro development of the plantlets. The addition of 0.93 μM/L 1,3-diphenylurea (DPU), 0.46 μM/L adenine (Ad), and 0.46 and 0.93 μM/L kinetin (Kin) resulted in the best shoot multiplication and elongation. In addition, the combination of 0.46 μM/L Kin, DPU, or Ad with gibberellic acid, in particular, 0.46 μM/L Ad + 0.58 μM/L GA₃ and 0.46 μM/L Kin + 1.15 μM/L GA₃, led to better bud and shoot multiplication. Moreover, the integration of the combinations of 0.46 μM/L Kin and auxins, namely 0.46 μM/L Kin + 2.85 μM/L indole-3-acetic acid (IAA), 0.46 μM/L Kin + 2.85 or 5.71 μM/L indole-3-butyric acid (IBA), and 0.46 μM/L Kin + 0.3 or 0.57 μM/L 1-naphthaleneacetic acid (NAA), in the culture medium led to better root development and optimized aerial growth. Finally, the in vitro plants from the medium containing N₃₀K + 0.46 μM/L Kin + 2.85 μM/L IAA were successfully acclimatized; these plants served as a source for repeating in vitro culture.

• Toxicological Research
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• 제14권3호
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• pp.357-363
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• 1998

The teratogenic potential of the anticonvulsant drug phenytoin (PHT) has been well documented both in the human and in the experimental animals. However there are few reports on the effects of PHT on embryonic development in rats in vitro. The present study was performed to evaluate the teratogenic effects of PHT using whole-embryo culture system in rats. Sprague-Dawley rat embryos were explanted on gestational day (GD) 9.5 and cultured for 48 hrs in the immediately centrifuged and heat-inactivated rat serum containing 0,25,50, or $100{\mu}g$ PHT/mL. At the end of culture period the embryos were scored for morphological development according to the procedure of Van Maele-Fabry, and their total protein contents were determined. At 100 ${\mu}$g/mL of culture medium. PHT caused significant reduction in developmental score and protein content of embryos and a high incidence morphological abnormalities (100%). Characteristic malformations included altered yolk and embryonic circulation, craniofacial hypoplasia, neural tube schisis, branchial arch defects, abnormal ratation, and limb bud hypoplasia, among others. There were no adverse effects on embryonic growth and development at concentrations of 25 and 50 ${\mu}$g /mL of culture medium. The results indicated that the dysmorphogenic effect of PHT on cultured embryos is due to a direct interference with embryonic development.

• Molecules and Cells
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• 제24권1호
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• pp.9-15
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• 2007

To investigate the effects of chitosan on the redifferentiation of dedifferentiated chondrocytes, we used chondrocytes obtained from a micromass culture system. Micromass cultures of chick wing bud mesenchymal cells yielded differentiated chondrocytes, but these dedifferentiated during serial monolayer subculture. When the dedifferentiated chondrocytes were cultured on chitosan membranes they regained the phenotype of differentiated chondrocytes. Expression of protein kinase $C{\alpha}$ ($PKC{\alpha}$) increased during chondrogenesis, decreased during dedifferentiation, and increased again during redifferentiation. Treatment of the cultures with phorbol 12-myristate 13-acetate (PMA) inhibited redifferentiation and down-regulated $PKC{\alpha}$. In addition, the expression of p38 mitogen-activated protein (MAP) kinase increased during redifferentiation, and its inhibition suppressed redifferentiation. These findings establish a culture system for producing chondrocytes, point to a new role of chitosan in the redifferentiation of dedifferentiated chondrocytes, and show that $PKC{\alpha}$ and p38 MAP kinase activities are required for chondrocyte redifferentiation in this model system.

• 식물조직배양학회지
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• 제25권5호
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• pp.305-308
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• 1998

키위의 엽육조직과 엽병조직을 치상하여 캘러스 및 부정아형성에 미치는 생장조절제의 효과를 조사한 결과 기관분 화성 캘러스형성은 2,4-D와 kinetin을 조합한 배지에서보다 NAA와 BA를 조합한 배지에서 양호하였고, 부정아 형성은 NAA와 BA를 조합한 배지에서만 형성되었으며 엽병조직보다 엽육조직을 배양하였을 때 반응이 양호하였다. 유도된 캘러스와 부정아로부터 신초의 형성은 MS기본배지에 0.1mg/L NAA와 2.0mg/L zeatin을 첨가한 배지에 계대배양하였을 때가 가장 효과적이었다. 신초의 발근은 1.0 mg/L IBA용액에 1시간 신초를 침지한 후 0.5 mg/L IAA와 0.1mg/L BA를 첨가한 배지에 배양하면 IBA용액에 침지처리 하지 않은 것보다 더 효과적이었으며 정상식물체로 발달하였다.

• 원예과학기술지
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• 제32권5호
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• pp.694-701
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• 2014

Allium hookeri L. (Alliaceae family) is an important ethnomedicinal plant native to the Himalayan region of Asia. The aim of this research was to establish a high-frequency plant regeneration system for in vitro propagation of A. hookeri. Among the tissue types examined, receptacle explants derived from immature flower buds showed the highest regeneration rate of shoots ($93.33{\pm}4.63%$), roots ($76.67{\pm}7.85%$), and calli ($80.00{\pm}7.43%$) when cultured on Gamborg B5 (B5) medium containing $10{\mu}M$ 6-benzylaminopurine (BA) + $1{\mu}M$ naphthalene acetic acid (NAA), $0.5{\mu}M$ BA + $5{\mu}M$ NAA, and $1{\mu}M$ BA + $10{\mu}M$ NAA, respectively. Shoot multiplication was superior when cultured in liquid rather than on solid medium and relatively high concentrations of BA, ranging from 5 to $10{\mu}M$. Efficient bulblet formation following root induction from shoot clumps was achieved with culture in liquid B5 medium containing 7% (w/v) sucrose. Regenerated bulblets were successfully acclimatized to ex vitro conditions with a greater than 95% survival rate. By this method, a maximum of 62 plantlets per receptacle could be propagated within 9 weeks of initial culture. The in vitro propagation system established in this study will promote A. hookeri biotechnology, including large-scale production of healthy and aseptic clones, preserving parental genotypes with desirable traits, and genetic manipulation to enhance medicinal value.

• 식물조직배양학회지
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• 제26권2호
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• pp.133-136
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• 1999

미선나무의 기내번식을 위하여 MS배지에 세 가지 싸이토키닌 (zeatin, kinetin 및 BA)을 세 가지 농도로 처리하여 액아 배양을 실시하였다. 줄기유도는 BA가 가장 효과적이었고, 생장은 zeatin이 좋았다. Kinetin은 2.0 및 5.0 mg/L 처리에서 줄기발생 효과가 있었으나 그 효과는 zeatin, BA에 비해 저조했다. 500 lux정도의 약광 하에서 배양은 싸이토키닌 처리에 관계없이 줄기의 생장을 촉진하였다. 발근은 IBA가 첨가된 1/2 GD배지에서 주효했다. 발근된 개체는 인공배양토에서 100% 활착되었고, 정상 생장이 가능했다. 이상의 결과에서 미선나무의 기내 번식이 가능함을 보여 주었다.

• 식물조직배양학회지
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• 제24권5호
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• pp.285-289
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• 1997

꿩의비름(Sedum-erythrostichum Miq.)의 잎과 줄기의 절편을 몇 가지의 호르몬이 첨가된 MS 배지에 배양하였다. 배양 2주후 2.0 mg/L. 2,4-D와 1.0 mg/L BA를 혼합한 배지에서 잎의 절편으로부터 100%의 캘러스가 형성되었다. 이 캘러스를 2.0 mg/L 2,4-D와 1.0 mg/L BA를 혼합한 배지로 계대배양하였을때 캘러스의 생장이 왕성하였다. 또한 2.0 mg/L NAA와 1.0 mg/L BA를 혼합한 배지로 계대배양한 캘러스로부터 부정아의 분화가 왕성하였다. 생장호르몬이 없는 배지에서 분화된 신초는 1.0 mg/L IAA를 첨가한 배지에서 발근하여 완전한 식물체로 생장하였다.

• Animal cells and systems
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• 제4권4호
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• pp.361-366
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• 2000

In order to investigate the role of protein kinase C (PKC) in chondrogenic differentiation, we examined the localization of PKC isoforms in a limb bud micromass culture system. PKC$\alpha$ is specifically localized in the regions which would become cartilage nodules, while PKC$\lambda/l$ and $\zeta$ display widespread distribution in the whole culture. Distribution of PKC$\alpha$ change along with promotion or inhibition of chondrogenesis by lysophosphatidylcholine or phorbol 12-myristate 13-acetate. On the other hand, localization of PKC$\lambda/l$ or $\zeta$ a was not changed by the modulation of chondrogenesis. Peanut agglutinin binding protein which is associated with cell aggregation during chondrogenesis was present in the cell condensation regions and its expression in those regions was influenced by PKC activity. Expression of fibronectin and N-cadherin in the cell condensing area were also affected by modulation of PKC activity. These results suggest involvement of PKC$\alpha$ in the cell condensation, possibly through regulating expression of fibronectin and N-cadherin.

• Journal of Forest and Environmental Science
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• 제37권2호
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• pp.148-153
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• 2021

This study was carried out to establish in vitro propagation system influenced by plant growth regulators through organogenesis with three different seed sources (China, Mongolia and Russia) for conservation of genetic resources in Northeast Asia. The experiment compared two different carbon sources (commercial sugar, sucrose), which showed no significant differences in germination rate. Induced adventitious buds from leaf segments were found to be highly effective when supplemented with 1.0 mg/L BA, 1.0 mg/L Kinetin, and 5.0 mg/L IAA, in the case of Chinese origin 96.8%, Russian origin R-1: 95.6%, R-2: 85.6%, and Mongolian origin M-2: 77.8%. It was effective in BA and Kinetin with supplemented with IAA, respectively. Shooting development was also efficient in Woody Plant Media (WPM) supplemented with 1.0 mg/L BA, 1.0 mg/L Kinetin and 5.0 mg/L IAA.