• Title/Summary/Keyword: PLD

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Phospholipases Dl and D2 Regulate Different Phases of Exocytosis in Mast Cells

  • Lee, Jun-Ho;Chang, Sung-Ho;Kim, Young-Mi;Her, Her Erk;Choi, Wahn-Soo
    • Proceedings of the PSK Conference
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    • 2003.10b
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    • pp.135.1-135.1
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    • 2003
  • The rat mast cell line RBL-2H3 contains both phospholipase D (PLD)1 and PLD2. Previous studies with this cell line indicated that expressed PLD1 and PLD2 are both strongly activated by stimulants of secretion. We now show by use of PLDs tagged with enhanced green fluorescent protein that PLD1, which is largely associated with secretory granules, redistributes to the plasma membrane in stimulated cells by processes reminiscent of exocytosis and fusion of granules with the plasma membrane. (omitted)

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Loss of phospholipase D2 impairs VEGF-induced angiogenesis

  • Lee, Chang Sup;Ghim, Jaewang;Song, Parkyong;Suh, Pann-Ghill;Ryu, Sung Ho
    • BMB Reports
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    • v.49 no.3
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    • pp.191-196
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    • 2016
  • Vascular endothelial growth factor (VEGF) is a key mediator of angiogenesis and critical for normal embryonic development and repair of pathophysiological conditions in adults. Although phospholipase D (PLD) activity has been implicated in angiogenic processes, its role in VEGF signaling during angiogenesis in mammals is unclear. Here, we found that silencing of PLD2 by siRNA blocked VEGF-mediated signaling in immortalized human umbilical vein endothelial cells (iHUVECs). Also, VEGF-induced endothelial cell survival, proliferation, migration, and tube formation were inhibited by PLD2 silencing. Furthermore, while Pld2-knockout mice exhibited normal development, loss of PLD2 inhibited VEGF-mediated ex vivo angiogenesis. These findings suggest that PLD2 functions as a key mediator in the VEGF-mediated angiogenic functions of endothelial cells.

Stimulation of Phospholipase D in HepG2 Cells After Transfection Using Cationic Liposomes

  • Lee, Sang Yoon;Lee, Yan;Choi, Joon Sig;Park, Jong Sang;Choi, Myung-Un
    • Bulletin of the Korean Chemical Society
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    • v.34 no.3
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    • pp.931-935
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    • 2013
  • Lipid events in liposome-mediated transfection (lipofection) are largely unknown. Here we studied whether phospholipase D (PLD), an important enzyme responsible for phospholipid breakdown, was affected during lipofection of HepG2 cells with a luciferase plasmid. Synthetic cholesterol (Chol) derivatives, including $3{\beta}$[L-ornithinamide-carbamoyl]Chol, [polyamidoamine-carbamoyl]Chol and $3{\beta}$[N-(N',N'-dimethylaminoethane)-carbamoyl]Chol, and a cationic lipid, N-[1-(2,3-dioleyloxy)propyl]-N,N,N-trimethylammonium chloride were mixed with a helper lipid dioleoylphosphatidylethanolamine to form respective cationic liposomes. All cationic liposomes were found to stimulate PLD. Although orders of magnitude effects of the cationic liposomes on PLD stimulation did not consistently match those on cytotoxicity and luciferase expression, a causal relationship between PLD activation and cytotoxic effect was remarkable. PLD stimulation by the cationic liposomes was likely due to their amphiphilic characters, leading to membrane perturbation, as supported by similar results obtained with other membrane-perturbing chemicals such as oleate, melittin, and digitonin. Our results suggest that lipofection induces cellular lipid changes such as a PLD-driven phospholipid turnover.

Electromagnetic properties of HTS coated conductors fabricated by PLD and MOD (PLD 및 MOD법으로 제조된 2세대 HTS 선재의 전자기 특성)

  • Oh, Sang-Soo;Hwang, Sun-Yuk;Song, Kyu-Jeong;Kang, Suk-Il;Ha, Dong-Woo;Ko, Rock-Kil;Park, Chan
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 2004.11a
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    • pp.65-68
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    • 2004
  • A lot of R&D efforts are being concentrated on the development of high performance HTS coated conductors(CC). Unlike the HTS Bi-2223 tape, a variety of processes have been tried to fabricate CC tapes. PLD and MOD are believed to be very effective methods, and high critical currents of long length CC tape have been reported. In this study, we prepared two kinds of YBCO CCs to evaluate electromagnetic property. One is YBCO tape deposited on IBAD template by PLD and the other is AMSC's MOD CC tape Critical current (Ic) in magnetic fields, its angular dependency, and n-value were measured and analyzed. Magnetic field property of Ic was appeared to be different due the fabrication process. MOD tape showed higher in-field property, n-value of both PLD and MOD tapes exponentially decreased with magnetic field. MOD tape showed higher n-value in whole magnetic fields.

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Development of OLED manufacturing process using PLD method (PLD법에 의한 OLED 제작 공정 개발)

  • Kim, Chang-Kyo;Noh, Il-Ho;Jang, Suk-Won;Hong, Chin-Soo;Yang, Sung-Jun
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 2004.11a
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    • pp.598-602
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    • 2004
  • Organic light entitling diode panel was fabricated using pulsed laser deposition (PLD) method Nd-YAG laser with Q-Switched and 355 nm pulse was used for the PLD. While TPD(N,N'-Di-[naphthaleny]-N, N'-diphenyl-benzidine) was used as a HTL(Hole transport layer), $Alq_3$(8-Hydroxyquinoline, Aluminum Salt) was used as EML/ETL(Emitting Layer/Electron Transport Layer) Organic pellet was fabricated and employed for the PLD method. The absorbances of the organic films were investigated and the measured absorbance values of TPD and $Alq_3$ films was 362 nm and 399 nm, respectively. The turn-on voltage of the OLED panel was 7.5 V and its luminance was $90\;cd/m^2$

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Research Trend of Oxide Magnetic Films with Atomically Controlled Pulsed Laser Deposition (원자층 제어 PLD를 이용한 산화물 자성 박막 연구의 동향)

  • Kim, Bong-Ju;Kim, Bog-G.
    • Journal of the Korean Magnetics Society
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    • v.22 no.4
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    • pp.147-156
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    • 2012
  • Recently, there have been considerable interests in various thin film growth techniques with atomically controllable thickness. Among them, atomically controlled pulsed laser deposition (PLD) technique is quite popular. We have developed advanced thin film growth technique using PLD and Reflection high energy electron diffraction (RHEED). Using the technique, the growth of oxide thin films with the precisely controllable thickness has been demonstrated. In addition, our technique can be applied to high quality thin film growth with minimal defect and bulk chemical composition. In this paper, our recent progresses as well as the current research trend on oxide thin films will be summarized.

The Effects of Single Component of Ginsenosides on the Mechanism of Mediator Release in the Allergic Hypersensitivity (인삼 사포닌 단일물질이 알러지 과민반응의 매개체 유리기전에 미치는 영향)

  • Ro, Jai-Youl;Kim, Kyung-Hwan
    • The Korean Journal of Pharmacology
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    • v.30 no.2
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    • pp.243-254
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    • 1994
  • Inflammatory diseases, allergic and asthmatic disorders are caused by the mediator release from the activation of the phospholipase C (PLC), phospholipase D (PLD), methyltransferase or adenylate cyclase etc. during IgG or IgE cross-linking of high affinity receptors on mast cells or basophil surface. One important enzyme activated after IgG or IgE receptor cross-linking is PLD, the enzyme which converts phosphatidylcholine (PC) to phosphatidic acid (PA). Under the hypothesis that these may be some differences in mediator release according to the difference in PLD activity, we attempted to confirm the ginseng saponin effects on the PLD activity. We examined the PLD activity during the passively sensitized mast cell activation in the presence of single component of ginsenosides $(Rc,\;Rg_1,\;Rg_2,\;Rg_3)$. We also measured the amount of mediators (histamine and leukotrienes) released by stimulating with ovalbumin (OA) or calcium ionophore (CaI), Guinea Pig lung mast cells were purified using enzyme digestion, count current elutriation, and discontinuous Percoll density gradient. In purified mast cells prelabeled with $[^3H]$ arachidonic acid or $[^3H]$ palmitic acid, PLD activity was assessed more directly by the production of labeled PEt by PLD-mediated transphosphatidylation in the presence of ethanol. Histanine release was determined by Spectrophotofluorometry, and leukotrienes by radioimmunoassay. The PLD activity during the passively sensitized mast cell activation is increased up to $3{\sim}5times$. The PLD activity during the passively sensitized mast cell activation in the presence of all ginsenosides is decreased up to $4{\sim}11$ times. $Rg_l\;and\;Rg_2$ ginsenoside pretreatment decreased histamine and leukotrienes by 50% in the OA-induced or by 40% in the Cal-induced mast cell after passively sensitization. Rc pretreatment poorly decreased histamine but leukotrienes decreased by 70% in the OA-induced or by 35% in the Cal-induced mast cell. $Rg_3$ ginsenoside pretreatment increased histamine release without challenging OA or Cal but leukotrienes decreased. These observations indicate that single unit of ginsenosldes may be an important contributor to inhibit the release of histamine and leukotrienes in the guinea pig lung mast cells, that inhibits the PLD-mediated formation of DAG evoked by mast cell activation.

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PLD implementation of the N-D digital filter with VHDL (VHDL을 이용한 다차원 디지털 필터의 PLD 구현)

  • Jeong, Jae-Gil
    • The Journal of Engineering Research
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    • v.6 no.1
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    • pp.111-124
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    • 2004
  • The advanced semiconductor technology and electronic design automation(EDA) tools make it possible to implement the system on the programmable logic devices. The electronic design method is also changing from schematic capture to hardware description language. In this paper, I present the architecture of multi-dimensional digital filter which can be efficiently implemented on PLDs. This is based on the former research results which are called algorithm decomposition technique. Algorithm decomposition technique is used to obtain the computational primitive from the state space equations of the multi-dimensional digital filtering algorithm. The obtained computational primitive is designed with VHDL. This can be used to implement the filtering system as a component. The designed filtering system is implemented on the PLD. Therefore, the filter can be upgradable on system. It is greatly reduced the time-to-market time of the system that is based on the multi-dimensional filter.

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A Potential Efficacy of Rebamipide as Anti-gastric Cancer Drug (위암치료제로서 rebamipide의 잠재적 효능)

  • Min, Do Sik
    • Journal of Life Science
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    • v.26 no.10
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    • pp.1214-1217
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    • 2016
  • Rebamipide is a mucosal-protective antiulcer drug, but its mechanism of action in gastric cancer remains elusive. CagA, a major virulence factor of Helicobacter pylori (H. pylori), is associated with the risk of gastric cancer. CagA protein is injected into gastric epithelial cells and deregulates a variety of cellular signaling molecules. CagA from H. pylori induces phospholipase D1 (PLD1) expression through NFκB activation in gastric epithelial cells, followed by invasion and proliferation of gastric epithelial cancer cells. Infection with cagA-positive H. pylori and expression of CagA enhances the binding of NFκB to the PLD1 promoter. Rebamipide abolishes H. pylori cagA-induced PLD1 expression via inhibition of binding of NFκB to the PLD1 promoter and also inhibits PLD activity. Moreover, rebamipide abolishes H. pylori CagA-induced β-catenin and the expression of a target cancer stem cell (CSC) marker gene via upregulation of miRNA-320a and -4496, followed by attenuation of self-renewal capacity of H. pylori CagA-infected gastric CSCs. In addition, rebamipide increases the chemosensitivity of CagA-expressed gastric CSCs and suppresses gastric carcinogenesis. Thus, it is speculated that rebamipide might show a potent efficacy as chemotherapeutic drug against gastric cancer cells. In this review, we summarizes recent results regarding the novel insights for the efficacy of rebamipide in gastric cancer cells.

Epigallocatechin Gallate Activates Phospholipase D in Glioma Cells (교세포에서 Epigallocatechin Gallate에 의한 포스포리파제 D의 활성화)

  • Kim, Shi-Yeon;Kim, Joonmo;Min, Do-Sik
    • Journal of Life Science
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    • v.13 no.6
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    • pp.924-932
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    • 2003
  • Epigallocatechin-3 Gallate (EGCG), a major constituent of green tea, has attracted increasing interest because of its many reported health benefits. Here we demonstrate for the first time that EGCG stimulates phospholipase D (PLD) activity in U87 human astroglioma cells. EGCG-induced PLD activation was abolished by the phospholipase C (PLC) inhibitor and a lipase inactive PLC-\gama1$ mutant, and was dependent on intracellular $Ca^{ 2+}$, and possibly involved $Ca^{ 2+}$ calmodulin-dependent protein kinase II (CaM kinase II). Interestingly, EGCG induced translocation of PLC-\gama1$ from the cytosol to the membrane and PLC-\gama1$interaction with PLD1. Taken together, these results demonstrate for the first time that in human astroglioma cells, EGCG regulates PLD activity via a signaling pathway involving a PLC-\gama1$ (inositol 1,4,5-trisphosphate-$Ca^{ 2+}$)-CaM kinase II-PLD pathway.