• The Korean Journal of Physiology and Pharmacology
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• 제2권4호
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• pp.411-417
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• 1998

The role of phospholipase ($A_2\;PLA_2$) in tumor cell growth was investigated using SK-N-MC human neuroblastoma cells. 4-Bromophenacyl bromide (BPB) and mepacrine (Mep), known $PLA_2$ inhibitors, suppressed growth of the tumor cells in a dose-dependent manner without a significant cytotoxicity. Melittin (Mel), a $PLA_2$ activator, enhanced the cell growth in a concentration-dependent fashion. The growth-enhancing effects of Mel were significantly reversed by the co-treatment with $PLA_2$ inhibitors. In addition, Mel induced intracellular $Ca^{2+}$ release from internal stores like as did serum, a known intracellular $Ca^{2+}$ agonist in the tumor cells. Intracellular $Ca^{2+}$ release induced by these agonists was significantly blocked by $PLA_2$ inhibitors at growth-inhibitory concentrations. Arachidonic acid (AA), a product of the $PLA_2-catalyzed$ reaction, induced cell growth enhancement and intracellular $Ca^{2+}$ release. These effects of AA were significantly blocked by BAPTA/AM, an intracellular $Ca^{2+}$ chelator. Taken together, these results suggest that the modulation of $PLA_2$ activity may be one of the regulatory mechanisms of cell growth in human neuroblastoma cells. Intracellular $Ca^{2+}$ may act as a key mediator in the $PLA_2-induced$ growth regulation.

• Membrane and Water Treatment
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• 제6권3호
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• pp.225-235
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• 2015

During low-pressure membrane treatments of cyanobacterial cells, including microfiltration (MF) and ultrafiltration (UF), there have reportedly been releases of intracellular compounds including cyanotoxins and compounds with an earthy-musty odor into the water, probably owing to cyanobacterial cell breakage retained on the membrane. However, to our knowledge, no information was reported regarding the effect of growth phase of cyanobacterial cells on the release of the intracellular compounds. In the present study, we used a geosmin-producing cyanobacterium, Anabaena smithii, to investigate the effect of the growth phase of the cyanobacterium on the release of intracellular geosmin during laboratory-scale MF experiments with the cells in either the logarithmic growth or stationary phase. Separate detection of damaged and intact cells revealed that the extent of cell breakage on the MF membrane was almost the same for logarithmic growth and stationary phase cells. However, whereas the geosmin concentration in the MF permeate increased after 3 h of filtration with cells in the logarithmic growth phase, it did not increase during filtration with cells in the stationary phase: the trend in the geosmin concentration in the MF permeate with time was much different between the logarithmic growth and stationary phases. Adsorption of geosmin to algogenic organic matter (AOM) retained on the MF membrane and/or pore blocking with the AOM were greater when the cells were in the stationary phase versus the logarithmic growth phase, the result being a decrease in the apparent release of intracellular geosmin from the stationary phase cells. In actual drinking water treatment plants employing membrane processes, more attention should be paid to the cyanobacterial cells in logarithmic growth phase than in stationary phase from a viewpoint of preventing the leakage of intracellular earthy-musty odor compounds to finished water.

• Bulletin of the Korean Chemical Society
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• 제32권2호
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• pp.524-530
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• 2011

In the present study, we demonstrate that SRM LC-MS/MS method developed by Luo et al. (ref. 10) can be successfully applied to the quantitative analysis of intracellular metabolites in E. coli that are collected at the exponential and stationary growth phases. A focus is given on measuring the changes in the concentrations of intracellular metabolites in batch cultures, which were induced during both the dynamically changing exponential and stationary growth phases. The following intracellular metabolites are quantified in the exponential and stationary phases of E. coli growth, using the SRM mode of a triple quadrupole mass spectrometer: glucose-1-phosphate, fructose-1,6-bisphosphate, phosphoenolpyruvate, pyruvate, acetyl-coenzyme A, 6-phosphogluconate, ribulose-5-phosphate, xylulose-5-phosphate, erythrose-4-phosphate. The determined intracellular metabolite concentration profiles are shown to be in a good agreement with the growth profiles of E. coli, which clearly indicates that SRM LC-MS/MS can be successfully used for following the metabolite changes induced at different growth stages.

• KSBB Journal
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• 제13권5호
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• pp.585-592
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• 1998

The effect of intracellular Ca2+ level on the hybridoma cell growth and monoclonal antibody(MAb) production was examined. For the manipulation of intracellular Ca2+ concentration, the cells were treated with A23187, ryanodine, and thapsigargin at about 1x106 cells/mL. The treated cells were recultivated by using the Iscove's Modified Dulbecco's Medium(MDM) containing 1.49mM CaCl2. The ryanodine-treated cells showed better cell growth, MAb concentration, and specific MAb productivity than others. In comparison with control, the maximum cell concentration, MAb concentration, and specific MAb productivity were increased by 40.6%, 48.1% and 83.3%, respectively. Confocal microscopic images of Fura-2/AM loaded cells indicate that the increase in intracellular Ca2+ level can enhance the MAb productivity by allowing the calcium influx into the endoplasmic reticulumn.

• 식물조직배양학회지
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• 제22권4호
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• pp.183-187
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• 1995

일일초 모상근배양에서 세포내 인산농도와 Catharanthine 생산과의 관계를 규명하였다. 모상근의 생장은 생장배지의 인산농도에 비례하여 증가하였다. Catharanthine 함량은 인산을 첨가하지 않은 배지에서 모상근을 배양하였을 때 최대값을 나타내었고 배지내의 인산농도를 증가함에 따라 비례적으로 감소하였다. 그리고 세포내의 인산농도에 비례하여 모상근의 생장은 증가하나 catharanthine의 함량은 감소하였다. Catharanthine 함량은 g 건조세포당 인산농도가 100mole 이하일 때에 현저하게 증가하였다. 이상의 결과로 세포내 인산농도는 모상근의 생장과 이차대사산물의 조절에 중요하게 관여함을 시사한다.

• Biotechnology and Bioprocess Engineering:BBE
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• 제5권1호
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• pp.44-47
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• 2000

Cell growth and DNA synthesis were studied from a cultured early- and late- pas- sage mouse aorta smooth muscle cell (MASMC) because the proliferation of vascular smooth muscle cell (VSMC) is a key factor in development of atherosclerosis. In this study, the cells were cultured in fetal bovine serum (FBS) and stimulated by growth factors such as thrombin and platelet-derived growth factor-BB (PDGF-BB). Compared to the number of early-passage MASMC (passage 3 to 9) the number of late-passage MASMC (passage 30 to 40) in a normal serum state was increased 2 fold at Day 1, 3 and 6 in culture, respectively. Incorporation of $[^3H]$ thymidine into DNA induced by serum, PDGF and thrombin in late-passage MASMC was greater than those in early-passage MASMC. We also examined whether intracellular zinc levels would be an aging factor or not. The intracellular zinc level in early- and late-passage MASMC was monitored by using the zinc probe dye N-(6-methoxy-8-quinolyl)-p-toluenesulfonamide. It is interested that late-passage MASMC increased the intracellular fluorescence level of zinc, more than the early passage MASMC did. The alterations of intracellular zinc level occur concurrently with changes in MASMC proliferation rate during aging. This data suggest that the age-associated changes in zinc concentrations may provide a new in vitro model for the study of smooth muscle cell differentiation.

• BMB Reports
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• 제32권2호
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• pp.173-180
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• 1999

The effects of agmatine on the enzymes responsible for the biosynthesis of polyamines, the resultant levels of polyamines, and their effect on the growth of DU145 human prostate tumor cells were investigated. When agmatine was added to the medium, ornithine decarboxylase (ODC, EC 4.1.1.17) activity was substantially reduced, but S-adenosylmethionine decarboxylase (SAMDC, EC 4.1.1.50) activity increased markedly. These changes in ODC and SAMDC activities were the result of an induction of ODC-antizyme and a decreased turnover rate of SAMDC in the presence of agmatine. Accordingly, there was a decrease in the intracellular levels of putrescine and spermidine but an increase in the intracellular level of spermine. Cell growth was markedly inhibited by agmatine treatment and this inhibition was not recovered by the addition of putrescine or spermidine. Our results suggest that agmatine alters the intracellular amounts of polyamine in the cells, closely related to the inhibition of cell growth.

• 미생물학회지
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• 제38권3호
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• pp.168-172
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• 2002

출아효모는 주변 환경 pH의 커다란 변화 속에서 적응할 수 있는 효과적인 체계를 지니고 있으며 SHC1 유전자는 알칼리 pH 조건에서 세포의 성장에 필요한 유전자 중에 하나임을 확인하였다. SHC1 유전자의 세포내 pH 조절 기작을 보다 구체적으로 알아보기 위하여 이 유전자가 소실된 돌연변이주를 제조하였다. 성장률의 차이가 나타나는 원인을 세포 내부의 pH 완충능력 결여에 의한 것으로 추측하고 pH 감수성 형광물질인 C.SNARE를 사용하여 외부 pH의 변화에 따른 세포 내부의 pH를 측정하였다. 알칼리 pH 완충효과는 소실 돌연변이의 경우는 야생종 대비 70% 수준을 보였다. 또한 pH 조절에 관여하는 효모세포 내부의 $Na^{+}$과 $K^{+}$의 농도를 원자흡광계를 사용하여 조사한 바, $K^{+}$ 이온의 경우에는 돌연변이주에 비하여 야생형 세포내에 더 많이 존재하는 것으로 나타났으나 $Na^{+}$ 이온의 경우는 별다른 차이점을 보이지 않았다. 이러한 결과는 $K^{+}$ 이온의 조절이 효모에서 세포내 pH조절 기작에 중요하며 SHC1 유전자는 이 $K^{+}$ 이온의 세포내 농도 유지에 관여하고 있다는 것을 제시해 주었다.

• Biomolecules & Therapeutics
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• 제16권1호
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• pp.21-27
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• 2008

Clotrimazole (CLT), a potent antifungal drug, is known to inhibit tumor cell proliferation. In the present study, we examined the role of intracellular $Ca^{2+}$ in CLT-induced cell cycle arrest of colon adenocarcinoma HT29 cells. CLT inhibited growth of HT29 cells in a concentration-dependent manner, which was associated with inhibition of cell cycle progression at the G(1)-S phase transition and an increase in the expression of cell cycle inhibitor proteins p27 and p53. CLT also suppressed the $Ca^{2+}$ overload by A23187, a calcium ionophore, suggesting its role in modulation of intracellular $Ca^{2+}$ concentration in HT29 cells. The simultaneous application of CLT and A23187 with addition of $CaCl_2$ (1mM) to the medium significantly reversed CLT-induced p27 and p53 protein level increase and growth suppression. Our results suggest that CLT induces cell cycle arrest of colon adenocarcinoma HT29 cells via induction of p27 and p53, which may, at least in part, be mediated by alteration of intracellular $Ca^{2+}$ level.

• 한국식품과학회지
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• 제28권1호
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• pp.122-126
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• 1996

Saccharomyces cerevisiae NS 2031의 유가식 배양에서 기질공급방법에 따라 효모 생육과 RNA 축적을 관찰하였다. Exponential feeding 형태에서 기질공급속도가 빠를 때 최종 배양 시간에서 균체량과 새포내 RNA 함량은 감소하는 경향을 나타내었으며, 배양시간이 경과함에 따라 균체내 RNA 함량은 전반적으로 감소하는 경향을 나타내었다. Exponential feeding 형태의 동일한 기질공급속도에서, 기질공급농도가 높을수록 최종 균체량은 감소하였으며, 균체수율(Yx/s)은 10%의 기질공급농도에서 0.47로 가장 높았다. 균체내 RNA 함량은 기질공급농도가 높을수록 증가하는 경향을 보였다. Parabolic feeding 형태에서는 기질공급속도가 빠를수록 균체량은 감소하였으나, 균체내 RNA 함량은 증가하여 exponential feeding 형태에서와 다른 경향을 나타내었다. 두가지 기질공급형태에서 균체생육에 가장 좋은 기질공급 program의 결과를 비교해 보면, 균체량, 균체수율, 세포내 RNA 함량을 높이려면 exponential feeding 형태가 parabolic feeding 형태보다 유리하였다. 또한, 유가식 배양에서 같은 instantaneous growth rate $({\mu}_{inst})$에서 균체내 RNA 함량을 비교하면, exponential feeding이 parabolic feeding보다 2%가량 높게 유지되어, 기질공급형태가 균체내 RNA 축적 생리에 큰 영향을 주고 있음을 알았다.