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        Inhibition of caspase-1-dependent apoptosis suppresses peste des petits ruminants virus replication

        Lingxia Li,Shengqing Li,Shengyi Han,Pengfei Li,Guoyu Du,Jinyan Wu,Xiaoan Cao,Youjun Shang 대한수의학회 2023 Journal of Veterinary Science Vol.24 No.5

        Background: Peste des petits ruminants (PPR), caused by the PPR virus (PPRV), is an acute and fatal contagious disease that mainly infects goats, sheep, and other artiodactyls. Peripheral blood mononuclear cells (PBMCs) are considered the primary innate immune cells. Objectives: PBMCs derived from goats were infected with PPRV and analyzed to detect the relationship between PPRV replication and apoptosis or the inflammatory response. Methods: Quantitative real-time polymerase chain reaction was used to identify PPRV replication and cytokines expression. Flow cytometry was conducted to detect apoptosis and the differentiation of CD4+ and CD8+ T cells after PPRV infection. Results: PPRV stimulated the differentiation of CD4+ and CD8+ T cells. In addition, PPRV induced apoptosis in goat PBMCs. Furthermore, apoptosis and the inflammatory response induced by PPRV could be suppressed by Z-VAD-FMK and Z-YVAD-FMK, respectively. Moreover, the virus titer of PPRV was attenuated by inhibiting caspase-1-dependent apoptosis and inflammation. Conclusions: This study showed that apoptosis and the inflammatory response play an essential role in PPR viral replication in vitro, providing a new mechanism related to the cell host response.

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        Selective harmonic active tuning control method for hybrid active power filters

        Luo, Zhaoxu,Liu, Yang,Li, Shengqing,Luo, Qin The Korean Institute of Power Electronics 2021 JOURNAL OF POWER ELECTRONICS Vol.21 No.6

        This paper proposes a selective harmonic active tuning control method for hybrid active power filters (HAPFs). A HAPF is composed of a voltage source inverter (VSI) and an LC filter. With this method, the VSI in the HAPF is controlled as a virtual capacitance that varies with the dominant harmonic frequencies. Thus, the LC filter can be forced to be tuning at these frequencies, which significantly improves the harmonic filtering characteristic of the LC filter. Meanwhile, to enhance the filtering performance in the case of a small power grid impedance or to damp the resonances between an LC filter and the grid impedance, the harmonics in the grid source current are detected and proportionally fed back to the controller, which brings about an effect equivalent to adding a series harmonic resistance on the grid source side. The proposed control method has the advantages of a simple control structure and easy implementation. Simulation and experimental results confirm the effectiveness and feasibility of the proposed method.

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        Aloe-emodin suppresses prostate cancer by targeting the mTOR complex 2.

        Liu, Kangdong,Park, Chanmi,Li, Shengqing,Lee, Ki Won,Liu, Haidan,He, Long,Soung, Nak Kyun,Ahn, Jong Seog,Bode, Ann M,Dong, Ziming,Kim, Bo Yeon,Dong, Zigang IRL Press] ; Oxford University Press 2012 Carcinogenesis Vol.33 No.7

        <P>Phosphatidylinositol 3-kinase (PI3-K) amplification and phosphatase and tensin homolog (PTEN) deletion-caused Akt activation contribute to the development of prostate cancer. Mammalian target of rapamycin complex 2 (mTORC2) is a kinase complex comprised of mTOR, Rictor, mSin1, mLST8/G관L and PRR5 and functions in the phosphorylation of Akt at Ser473. Herein, we report that mTORC2 plays an important role in PC3 androgen refractory prostate cell proliferation and anchorage-independent growth. Aloe-emodin, a natural compound found in aloe, inhibited both proliferation and anchorage-independent growth of PC3 cells. Protein content analysis suggested that activation of the downstream substrates of mTORC2, Akt and PKC관, was inhibited by aloe-emodin treatment. Pull-down assay and in vitro kinase assay results indicated that aloe-emodin could bind with mTORC2 in cells and inhibit its kinase activity. Aloe-emodin also exhibited tumor suppression effects in vivo in an athymic nude mouse model. Collectively, our data suggest that mTORC2 plays an important role in prostate cancer development and aloe-emodin suppresses prostate cancer progression by targeting mTORC2.</P>

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