• Title/Summary/Keyword: TAT 1

Search Result 183, Processing Time 0.023 seconds

Tat-Fused Recombinant Human SAG Prevents Dopaminergic Neurodegeneration in a MPTP-Induced Parkinson's Disease Model

  • Sohn, Eun Jeong;Shin, Min Jea;Kim, Dae Won;Ahn, Eun Hee;Jo, Hyo Sang;Kim, Duk-Soo;Cho, Sung-Woo;Han, Kyu Hyung;Park, Jinseu;Eum, Won Sik;Hwang, Hyun Sook;Choi, Soo Young
    • Molecules and Cells
    • /
    • v.37 no.3
    • /
    • pp.226-233
    • /
    • 2014
  • Excessive reactive oxygen species (ROS) generated from abnormal cellular process lead to various human diseases such as inflammation, ischemia, and Parkinson's disease (PD). Sensitive to apoptosis gene (SAG), a RING-FINGER protein, has anti-apoptotic activity and anti-oxidant activity. In this study, we investigate whether Tat-SAG, fused with a Tat domain, could protect SH-SY5Y neuroblastoma cells against 1-methyl-4-phenylpyridinium ($MPP^+$) and dopaminergic (DA) neurons in the substantia nigra (SN) against 1-methyl-4-phenyl-1,2,3,6-tetra-hydropyridine (MPTP) toxicity. Western blot and immunohistochemical analysis showed that, unlike SAG, Tat-SAG transduced efficiently into SH-SY5Y cells and into the brain, respectively. Tat-SAG remarkably suppressed ROS generation, DNA damage, and the progression of apoptosis, caused by $MPP^+$ in SH-SY5Y cells. Also, immunohistochemical data using a tyrosine hydroxylase antibody and cresyl violet staining demonstrated that Tat-SAG obviously protected DA neurons in the SN against MPTP toxicity in a PD mouse model. Tat-SAG-treated mice showed significant enhanced motor activities, compared to SAG- or Tat-treated mice. Therefore, our results suggest that Tat-SAG has potential as a therapeutic agent against ROS-related diseases such as PD.

The Primary Study on Chiljung of Inherent Basic Emotion (내재된 기본 감정으로서의 칠정(七情)에 관한 초보적 연구)

  • Jung, Jong-Hyo;Choi, Geum-Ae;Kim, Kyung-Su;Kim, Kyeong-Ok
    • Journal of Oriental Neuropsychiatry
    • /
    • v.20 no.1
    • /
    • pp.107-118
    • /
    • 2009
  • Objectives : One's mind turned over by environment and personal relationship is Emotion. Emotion is composed by several basic feelings. This basic feeling is called Chiljung in Oriental Medicine. This study is confirmed difference of Chiljung by Constitution. Methods : 80 persons of Oriental medicine university students were tested by Qustionnaire for the Sasang Constitution Classification II(QSCCII) and Thematic Apperception Test(TAT). Constitution is distinguished by QSCCII. 11 pieces picture of TAT were showed one minute and then had person to discribe one's feelings. Two data were analyzed by statistical analysis. Results : Result is as follows, tested TAT about expression of inherent basic emotion. 1. It has relations with cognitive thought process 2. Expression of Chiljung has some relations with constitution and personal trait. Conclusion : Chiljung of inherent basic emotion is cognitive and has difference between constitutions by TAT.

  • PDF

Tat-Thioredoxin-like protein 1 attenuates ischemic brain injury by regulation of MAPKs and apoptosis signaling

  • Hyun Ju Cha;Won Sik Eum;Gi Soo Youn;Jung Hwan Park;Hyeon Ji Yeo;Eun Ji Yeo;Hyun Jung Kwon;Lee Re Lee;Na Yeon Kim;Su Yeon Kwon;Yong-Jun Cho;Sung-Woo Cho;Oh-Shin Kwon;Eun Jeong Sohn;Dae Won Kim;Duk-Soo Kim;Yu Ran Lee;Min Jea Shin;Soo Young Choi
    • BMB Reports
    • /
    • v.56 no.4
    • /
    • pp.234-239
    • /
    • 2023
  • Thioredoxin-like protein 1 (TXNL1), one of the thioredoxin superfamily known as redox-regulator, plays an essential in maintaining cell survival via various antioxidant and anti-apoptotic mechanisms. It is well known that relationship between ischemia and oxidative stress, however, the role of TXNL1 protein in ischemic damage has not been fully investigated. In the present study, we aimed to determine the protective role of TXNL1 against on ischemic injury in vitro and in vivo using cell permeable Tat-TXNL1 fusion protein. Transduced Tat-TXNL1 inhibited ROS production and cell death in H2O2-exposed hippocampal neuronal (HT-22) cells and modulated MAPKs and Akt activation, and pro-apoptotic protein expression levels in the cells. In an ischemia animal model, Tat-TXNL1 markedly decreased hippocampal neuronal cell death and the activation of astrocytes and microglia. These findings indicate that cell permeable Tat-TXNL1 protects against oxidative stress in vitro and in vivo ischemic animal model. Therefore, we suggest Tat-TXNL1 can be a potential therapeutic protein for ischemic injury.

Transduced Tat-Annexin protein suppresses inflammation-associated gene expression in lipopolysaccharide (LPS)-stimulated Raw 264.7 cells

  • Lee, Sun-Hwa;Kim, Dae-Won;Back, Su-Sun;Hwang, Hyun-Sook;Park, Eun-Young;Kang, Tae-Cheon;Kwon, Oh-Shin;Park, Jong-Hoon;Cho, Sung-Woo;Han, Kyu-Hyung;Park, Jin-Seu;Eum, Won-Sik;Choi, Soo-Young
    • BMB Reports
    • /
    • v.44 no.7
    • /
    • pp.484-489
    • /
    • 2011
  • Annexin-1 (ANX1) is an anti-inflammatory protein as well as an important modulator in inflammation. However, the precise action of ANX1 remains unclear. To elucidate the protective effects of ANX1 on lipopolysaccharide (LPS)-induced murine macrophage Raw 264.7 cells, we constructed a cell-permeable Tat-ANX1 protein. The transduced Tat-ANX1 protein markedly inhibited the expression of cyclooxygenase-2, production of prostaglandin $E_2$, and generation of pro-inflammatory cytokines in the cells. Furthermore, transduced Tat-ANX1 protein caused a significant reduction in the activation of nuclear factor-kappa B (NF-${\kappa}B$) and mitogen-activated protein kinase (MAPK). The results indicate that Tat-ANX1 inhibits the production of inflammatory response cytokines and enzymes by blocking NF-${\kappa}B$ and MAPK. Therefore, Tat-ANX1 protein may be useful as a therapeutic agent against various inflammatory diseases.

Liposome/Tat Complex for Facilitating Genistein Uptake into B16 Melanoma Cells

  • Park, Young-Mi;Kang, Myung-Joo;Moon, Ki-Young;Park, Sang-Han;Kang, Mean-Hyung;Choi, Young-Wook
    • Journal of Pharmaceutical Investigation
    • /
    • v.41 no.4
    • /
    • pp.205-210
    • /
    • 2011
  • Genistein (GT), a major isoflavone found in soybeans, has a potent antioxidant effect that protects the skin from UV-induced damages and malignant melanoma. In order to enhance the cellular uptake of GT, liposome/Tat complexes were prepared by an electrostatic interaction of anionic liposome (DMPC/DCP, 9:1 in molar ratio) with Tat peptide (0.02 to 0.08 mole), one of the well-known cell penetrating peptide (CPP). As the amount of Tat increased, the size increased but the zeta potential decreased. In vitro release study with dialysis membrane elicited GT release from liposomal preparations in a controlled manner. The addition of Tat increased GT release, especially for the initial period. In the cellular uptake study by incubating B16 melanoma cells with various liposomal preparations containing GT, B16 melanoma cells demonstrated a time-dependent increase of drug accumulation. Compared to the aqueous GT suspension, intracellular uptake was substantially enhanced by anionic liposomal formulation and further increased by the complex formulation. Therefore, liposome/ Tat complex might be a good candidate for facilitating intracellular drug delivery.

Suppression of 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced skin inflammation in mice by transduced Tat-Annexin protein

  • Lee, Sun-Hwa;Kim, Dae-Won;Eom, Seon-Ae;Jun, Se-Young;Park, Mee-Young;Kim, Duk-Soo;Kwon, Hyung-Joo;Kwon, Hyeok-Yil;Han, Kyu-Hyung;Park, Jin-Seu;Hwang, Hyun-Sook;Eum, Won-Sik;Choi, Soo-Young
    • BMB Reports
    • /
    • v.45 no.6
    • /
    • pp.354-359
    • /
    • 2012
  • We examined that the protective effects of ANX1 on 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced skin inflammation in animal models using a Tat-ANX1 protein. Topical application of the Tat-ANX1 protein markedly inhibited TPA-induced ear edema and expression levels of cyclooxygenase-2 (COX-2) as well as pro-inflammatory cytokines such as interleukin-1 beta (IL-$1{\beta}$), IL-6, and tumor necrosis factor-alpha (TNF-${\alpha}$). Also, application of Tat-ANX1 protein significantly inhibited nuclear translocation of nuclear factor-kappa B (NF-${\kappa}B$) and phosphorylation of p38 and extracellular signal-regulated kinase (ERK) mitogen-activated protein kinase (MAPK) in TPA-treated mice ears. The results indicate that Tat-ANX1 protein inhibits the inflammatory response by blocking NF-${\kappa}B$ and MAPK activation in TPA-induced mice ears. Therefore, the Tat-ANX1 protein may be useful as a therapeutic agent against inflammatory skin diseases.

ON SIMILARITY INVARIANTS OF EP MATRICES

  • Rajian, C.;Chelvam, T. Tamizh
    • East Asian mathematical journal
    • /
    • v.23 no.2
    • /
    • pp.207-212
    • /
    • 2007
  • We describe the class of invertible matrices T such that $TAT^{-1}$ is EPr, for a given EPr matrix A of order n. Necessary and sufficient condition is determined for $TAT^{-1}$ to be EP for an arbitrary matrix A of order n.

  • PDF

Modified SOD for Cosmeceuticals

  • Kang, Nae-Gyu;Lim, Jun-Man;Chang, Min-Youl;Park, Sun-Gyoo;Cho, Wan-Goo;Kang, She-Hoon;Park, Soo-Young
    • Proceedings of the SCSK Conference
    • /
    • 2003.09a
    • /
    • pp.630-644
    • /
    • 2003
  • A human Cu, Zn-superoxide dismutase (Cu, Zn-SOD) was fused with a Tat PTD of HIV-1 to produce a novel anti-aging ingredient, Tat-SOD for cosmeceuticals. Test of stability and evaluation of transduction efficacy and enzymatic activity suggest Tat-SOD is an effective active ingredient for anti-aging treatment.

  • PDF

HIV-1 Tat-mediated protein transduction of human brain creatine kinase into PC12 cells

  • Jeong, Min-Seop;Kim, Dae-Won;Lee, Min-Jung;Lee, Yeom-Pyo;Kim, So-Young;Lee, Sun-Hwa;Jang, Sang-Ho;Lee, Kil-Soo;Park, Jin-Seu;Kang, Tae-Cheon;Cho, Sung-Woo;Kwon, Oh-Shin;Eum, Won-Sik;Choi, Soo-Young
    • BMB Reports
    • /
    • v.41 no.7
    • /
    • pp.537-541
    • /
    • 2008
  • Epilepsy is characterized by the presence of spontaneous episodes of abnormal neuronal discharges and its pathogenic mechanisms remain poorly understood. Recently, we found that the expression of creatine kinase (CK) was markedly decreased in an epilepsy animal model using proteomic analysis. A human CK gene was fused with a HIV-1 Tat peptide to generate an in-frame Tat-CK fusion protein. The purified Tat-CK fusion protein was efficiently transduced into PC12 cells in a time- and dose-dependent manner when added exogenously to culture media. Once inside the cells, the transduced Tat-CK fusion protein was stable for 48 h. Moreover, the Tat-CK fusion protein markedly increased endogenous CK activity levels within the cells. These results suggest that Tat-CK provides a strategy for the therapeutic delivery of proteins in various human diseases including the delivery of CK for potential epilepsy treatment.