• Journal of Veterinary Science
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• 제21권6호
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• pp.88.1-88.13
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• 2020

Background: Listeria monocytogenes is a gram-positive bacterium that causes listeriosis mainly in immunocompromised hosts. It can also cause foodborne outbreaks and has the ability to adapt to various environments. Peptide uptake in gram-positive bacteria is enabled by oligopeptide permeases (Opp) in a process that depends on ATP hydrolysis by OppD and F. Previously a putative protein Lmo2193 was predicted to be OppD, but little is known about the role of OppD in major processes of L. monocytogenes, such as growth, virulence, and biofilm formation. Objectives: To determine whether the virulence traits of L. monocytogenes are related to OppD. Methods: In this study, Lmo2193 gene deletion and complementation strains of L. monocytogenes were generated and compared with a wild-type strain for the following: adhesiveness, invasion ability, intracellular survival, proliferation, 50% lethal dose (LD₅₀) to mice, and the amount bacteria in the mouse liver, spleen, and brain. Results: The results showed that virulence of the deletion strain was 1.34 and 0.5 orders of magnitude higher than that of the wild-type and complementation strains, respectively. The function of Lmo2193 was predicted and verified as OppD from the ATPase superfamily. Deletion of lmo2193 affected the normal growth of L. monocytogenes, reduced its virulence in cells and mice, and affected its ability to form biofilms. Conclusions: Deletion of the oligopeptide transporter Lmo2193 decreases the virulence of L. monocytogenes. These effects may be related to OppD's function, which provides a new perspective on the regulation of oligopeptide transporters in L. monocytogenes.

• BMB Reports
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• 제55권10호
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• pp.506-511
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• 2022

Advanced hepatocellular carcinoma (HCC) is among the most challenging cancers to overcome, and there is a need for better therapeutic strategies. Among the different cancer drugs that have been used in clinics, sorafenib is considered the standard first-line drug for advanced HCC. Here, to identify a chemical compound displaying a synergistic effect with sorafenib in HCC, we screened a focused chemical library and found that MG149, a histone acetyltransferase inhibitor targeting the MYST family, exhibited the most synergistic anticancer effect with sorafenib on HCC cells. The combination of sorafenib and MG149 exerted a synergistic anti-proliferation effect on HCC cells by inducing apoptotic cell death. We revealed that cotreatment with sorafenib and MG149 aggravated endoplasmic reticulum (ER) stress to promote the death of HCC cells rather than adaptive cell survival. In addition, combined treatment with sorafenib and MG149 significantly increased the intracellular levels of unfolded proteins and reactive oxygen species, which upregulated ER stress. Collectively, these results suggest that MG149 has the potential to improve the efficacy of sorafenib in advanced HCC via the upregulation of cytotoxic ER stress.

• Biomolecules & Therapeutics
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• 제31권5호
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• pp.484-495
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• 2023

Idiopathic pulmonary fibrosis (IPF) can be defined as a progressive chronic pulmonary disease showing scarring in the lung parenchyma, thereby resulting in increase in mortality and decrease in the quality of life. The pathophysiologic mechanism of fibrosis in IPF is still unclear. Repetitive microinjuries to alveolar epithelium with genetical predisposition and an abnormal restorative reaction accompanied by excessive deposition of collagens are involved in the pathogenesis. Although the two FDA-approved drugs, pirfenidone and nintedanib, are under use for retarding the decline in lung function of patients suffered from IPF, they are not able to improve the survival rate or quality of life. Therefore, a novel therapeutic agent acting on the major steps of the pathogenesis of disease and/or, at least, managing the clinical symptoms of IPF should be developed for the effective regulation of this incurable disease. In the present review, we tried to find a potential of managing the clinical symptoms of IPF by natural products derived from medicinal plants used for controlling the pulmonary inflammatory diseases in traditional Asian medicine. A multitude of natural products have been reported to exert an antifibrotic effect in vitro and in vivo through acting on the epithelial-mesenchymal transition pathway, transforming growth factor (TGF)- β-induced intracellular signaling, and the deposition of extracellular matrix. However, clinical antifibrotic efficacy of these natural products on IPF have not been elucidated yet. Thus, those effects should be proven by further examinations including the randomized clinical trials, in order to develop the ideal and optimal candidate for the therapeutics of IPF.

• Journal of Microbiology and Biotechnology
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• 제33권9호
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• pp.1130-1140
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• 2023

Among the AAA+ proteases in bacteria, FtsH is a membrane-bound ATP-dependent metalloprotease, which is known to degrade many membrane proteins as well as some cytoplasmic proteins. In the intracellular pathogen Salmonella enterica serovar Typhimurium, FtsH is responsible for the proteolysis of several proteins including MgtC virulence factor and MgtA/MgtB Mg²⁺ transporters, the transcription of which is controlled by the PhoP/PhoQ two-component regulatory system. Given that PhoP response regulator itself is a cytoplasmic protein and also degraded by the cytoplasmic ClpAP protease, it seems unlikely that FtsH affects PhoP protein levels. Here we report an unexpected role of the FtsH protease protecting PhoP proteolysis from cytoplasmic ClpAP protease. In FtsH-depleted condition, PhoP protein levels decrease by ClpAP proteolysis, lowering protein levels of PhoP-controlled genes. This suggests that FtsH is required for normal activation of PhoP transcription factor. FtsH does not degrade PhoP protein but directly binds to PhoP, thus sequestering PhoP from ClpAP-mediated proteolysis. FtsH's protective effect on PhoP can be overcome by providing excess ClpP. Because PhoP is required for Salmonella's survival inside macrophages and mouse virulence, these data implicate that FtsH's sequestration of PhoP from ClpAP-mediated proteolysis is a mechanism ensuring the amount of PhoP protein during Salmonella infection.

• 한국가금학회지
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• 제50권4호
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• pp.213-229
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• 2023

본 연구는 한국 토종닭을 대상으로 부리 다듬기 여부와 교배조합이 생산능력 및 스트레스 반응 정도에 미치는 영향을 살펴 보고자 한 것이다. 시험은 6개의 토종닭 교배조합 248수를 대상으로 부리 다듬기를 실시한 그룹과 하지 않은 그룹으로 나누고, 이들의 생존율, 체중, 산란율, 난질, 깃털 손상도, HSP-70 유전자 발현량, H/L ratio 및 세포 내 DNA 손상률을 조사하여 비교 분석하였다. 분석 결과, 부리 다듬기를 한 그룹이 하지 않은 그룹보다 생존율 및 산란지수는 유의하게 높았고, 깃털 손상도 및 DNA 손상률은 유의하게 낮았다(P<0.05). 반면 육성기 이후 체중, 일계산란율, 난질, HSP-70 유전자 발현율 및 H/L ratio는 부리 다듬기 여부에 따른 차이가 없는 것으로 나타났다. 한편, 교배조합 간에는 생존율, 체중, 깃털 손상도, 난질 및 DNA 손상률에 유의한 차이를 보이고(P<0.05), 산란율, HSP-70 유전자 발현율 및 H/L ratio의 차이는 없는 것으로 나타났다. 생존율, 깃털 손상도 및 DNA 손상률은 부리 다듬기와 교배조합 간의 상호작용이 있는 것으로 나타났다. 이상의 분석 결과로부터 토종닭의 부리 다듬기가 생산능력에 긍정적인 영향을 미치고, 스트레스 반응 정도에 있어서 육성기 이후부터는 부리 다듬기가 스트레스 요인으로 작용하지 않거나, 오히려 스트레스감소 요인으로 작용하는 것으로 판단된다. 또한 토종닭 교배조합 간에 생산능력 및 스트레스 반응 정도의 차이는 있으나 조합별 부리 다듬기가 이들에 미치는 영향은 거의 비슷한 것으로 보인다.

• 생명과학회지
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• 제27권8호
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• pp.945-950
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• 2017

유기용매 내성 Pseudomonas sp. BCNU 106은 독성 용매에 의해 일부 생장이 제한되므로 다양한 생존전략이 필요하다. 이러한 한계를 극복하기 위한 하나의 전략으로 외인성 트레할로오스를 사용하는 것이다. Cyclohexane 존재하에 세포내 트레할로스 함량은 12시간 배양했을 때 181.88 mM로 가장 높게 측정되었고, 세포외 트레할로스 함량은 12시간에서 16시간 사이에 급격하게 감소하였다. 또한 1%(v/v) cyclohexane, hexane, propylbenzene 및 m-xylene 존재하에 0.1 M 트레할로스가 첨가된 LB 배지에서 Pseudomonas sp. BCNU 106 균주의 생장은 트레할로스가 첨가되지 않은 대조군에 비해 각각 89.94, 89.72, 91.25 및 118.9 배 증가하였으며, cyclohexane 및 hexane 존재하에서 0.05 M 트레할로스를 첨가했을 때 4시간 동안 각각 80과 90% 이상의 높은 생존율을 보였다. 이는 배지에 첨가된 트레할로스가 세포 내로 이동하면서 cyclohexane, hexane, propylbenzene 및 m-xylene 스트레스에 대해 방어작용을 한 것으로 보인다. 따라서 성장배지에 트레할로스를 첨가함에 따라 Pseudomonas sp. BCNU 106의 유기용매 내성이 향상되어 생물전환 및 생물분해에 대한 잠재적인 생물촉매로 사용 가능할 것이다.

• Parasites, Hosts and Diseases
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• 제58권3호
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• pp.237-247
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• 2020

Dendritic cell is one of the first innate immune cell to encounter T. gondii after the parasite crosses the host intestinal epithelium. T. gondii requires intact DC as a carrier to infiltrate into host central nervous system (CNS) without being detected or eliminated by host defense system. The mechanism by which T. gondii avoids innate immune defense of host cell, especially in the dendritic cell is unknown. Therefore, we examined the role of host PI3K/AKT signaling pathway activation by T. gondii in dendritic cell. T. gondii infection or T. gondii excretory/secretory antigen (TgESA) treatment to the murine dendritic cell line DC2.4 induced AKT phosphorylation, and treatment of PI3K inhibitors effectively suppressed the T. gondii proliferation but had no effect on infection rate or invasion rate. Furthermore, it is found that T. gondii or TgESA can reduce H₂O₂-induced intracellular reactive oxygen species (ROS) as well as host endogenous ROS via PI3K/AKT pathway activation. While searching for the main source of the ROS, we found that NADPH oxidase 4 (NOX4) expression was controlled by T. gondii infection or TgESA treatment, which is in correlation with previous observation of the ROS reduction by identical treatments. These findings suggest that the manipulation of the host PI3K/AKT signaling pathway and NOX4 expression is an essential mechanism for the down-regulation of ROS, and therefore, for the survival and the proliferation of T. gondii.

• 한국약용작물학회지
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• 제10권3호
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• pp.206-211
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• 2002

박하와 배초향 정유의 보존료로서의 이용가능성을 타진하기 위해 그 성분조성을 GC-MSD 분석에 의해 실험한 결과 박하 정유의 주된 성분은 isomenthol로서 전체 정유성분 중 25.84%, menthol이 25.48%이었으며 배초향 정유에는 estragole이 79.83%, limonene이 0.12%함유되어 있었다. 2, 5, 10 mg 농도에서도. E. coli O157 : H7 ATCC 43895에 대한 박하 정유의 생육저해환은 $(9{\sim}14\;mm)$, 배초향 정유는 $(10{\sim}18\;mm)$, S. typhimurium ATCC 7988에 대해서는 박하 정유가 $(9{\sim}13\;mm)$, 배초향 정유가 $(13{\sim}20\;mm으로 나타나 두 정유성분 모두 농도 의존적으로 항균작용을 나타내었다. 생균수 측정 실험에서 박하 정유는 2 mg이하의 저농도에서 9시간까지 세균의 증식을 억제시켰으며 5 mg 이상의 농도에서는 9시간이후 E. coli O157 : H7 ATCC 43895와 S. typhimurium ATCC 7988을 모두 사멸시켰다. 배초향 정유는 2 mg이하의 농도에서 12시간까지 세균의 증식이 억제되었고 5 mg이상의 농도에서는 6시간이후 세균이 사멸되었다. E. coli O157 : H7 ATCC 43895에 대한 박하와 배초향 정유 성분의 항균작용을 전자현미경 촬영에 의해 확인한 결과 형태학적인 변화와 세포막과 세포벽의 분리 및 세포내용물 유실이 관찰되어 두 정유성분의 항균효과를 관찰할 수 있었다.

• Asian Pacific Journal of Cancer Prevention
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• 제15권1호
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• pp.265-271
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• 2014

Interleukin-7 (IL-7) is a potent anti-apoptotic cytokine that enhances immune effector cell functions and is essential for lymphocyte survival. While it known to induce differentiation and proliferation in some haematological malignancies, including certain types of leukaemias and lymphomas, little is known about its role in solid tumours, including breast cancer. In the current study, we investigated whether IL-7 could enhance the in vivo antitumor activity of tumor-reactive $CD8^+$ T cells with induction of IFN-${\gamma}$ in a murine breast cancer model. Human IL-7 cDNA was constructed into the eukaryotic expression plasmid pcDNA3.1, and then the recombinational pcDNA3.1-IL-7 was intratumorally injected in the TM40D BALB/C mouse graft model. Serum and intracellular IFN-${\gamma}$ levels were measured by ELISA and flow cytometry, respectively. $CD8^+$ T cell-mediated cytotoxicity was analyzed using the MTT method. Our results showed that IL-7 administration significantly inhibited tumor growth from day 15 after direct intratumoral injection of pcDNA3.1-IL-7. The anti-tumor effect correlated with a marked increase in the level of IFN-${\gamma}$ and breast cancer cells-specific CTL cytotoxicity. In vitro cytotoxicity assays showed that IL-7-treatment could augment cytolytic activity of $CD8^+$ T cells from tumor bearing mice, while anti-IFN-${\gamma}$ blocked the function of $CD8^+$ T cells, suggesting that IFN-${\gamma}$ mediated the cytolytic activity of $CD8^+$ T cells. Furthermore, in vivo neutralization of $CD8^+$ T lymphocytes by CD8 antibodies reversed the antitumor benefit of IL-7. Thus, we demonstrated that IL-7 exerts anti-tumor activity mainly through activating $CD8^+$ T cells and stimulating them to secrete IFN-${\gamma}$ in a murine breast tumor model. Based on these results, our study points to a potential novel way to treat breast cancer and may have important implications for clinical immunotherapy.

• 동의신경정신과학회지
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• 제21권2호
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• pp.125-140
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• 2010

Objectives : The purpose of this study is to examine from various angles the protective effect of Gastrodia elata Blume (GEB) against nerve cell death induced by $\beta$-amyloid by using the cell line SH-SY5Y, which is commonly utilized for toxicity testing in nerve cells, and to find out its mechanism of action. Methods : To begin with, as a result of assessing the rate of cell survival by employing MTT reduction assay, the treatment with $\beta$-amyloid at different concentrations caused cytotoxicity, which was inhibited by preprocessing GEB extract. In addition, after $\beta$-amyloid was processed with the cell SH-SY5Y, apoptosis progressed, which was reduced effectively by processing GEB extract. Results : When cytotoxicity was caused by using hydrogen peroxide, a representative ROS, in order to examine the antioxidant effect of GEB, its protective effect was also observed. Apart from ROS, reactive nitrogen species (RNS) are also known to play a crucial role in nerve cell death. The treatment with the NO donor SNAP increased the production of nitric oxide and the expression of iNOS, which was also inhibited by GEB extract. Meanwhile, as an attempt to find out the mechanism of action explaining the antioxidant effect, the intracellular antioxidant enzyme expressions were measured by RT-PCR, which showed that GEB extract increased the expressions of heme oxygenase-1, GAPDH and $\gamma$-glutamate cysteine ligase. Lastly, GEB extract had a protective effect against impaired memory induced by scopolamine in animal models (in vivo). Conclusions : These findings indicate that GEB has a protective effect against the death of cranial nerve cells, suggesting possibilities for the prevention and treatment of AD.