• Korean Journal of Mathematics
• /
• v.13 no.1
• /
• pp.1-11
• /
• 2005

The purpose of the present paper is to introduce a new concept of the E($^*{\kappa}$)-connection ${\Gamma}^{\nu}_{{\lambda}{\mu}}$, which is both Einstein and ($^*{\kappa}$)-connection, and to obtain a necessary and sufficient condition for the existence of the unique E($^*{\kappa}$)-connection in $n-^*g$-UFT. Next, under this condition, we shall obtain a surveyable tensorial representation of the unique E($^*{\kappa}$)-connection in $n-^*g$-UFT.

• Korean Journal of Mathematics
• /
• v.12 no.1
• /
• pp.23-32
• /
• 2004

Let (B, $m_B$, ${\kappa}$) be a maximal commutative ${\kappa}$-subalgebra of a matrix algebra $M_n(\kappa)$. We will construct a maximal commutative ${\kappa}$-subalgebra (R, $m$, ${\kappa}$) of $M_n+3(\kappa)$ from the algebra B such that the algebra R has dimension greater than the dimension of B by 3. Moreover, we will show a $C_i$-construction doesn't imply a $C^3_2$-construction for $i=1,2$.

• Tuberculosis and Respiratory Diseases
• /
• v.50 no.1
• /
• pp.52-66
• /
• 2001

Background : NF-${\kappa}B$ is the most important transcriptional factor in IL-8 gene expression. Triptolide is a new compound that recently has been shown to inhibit NF-${\kappa}B$ activation. The purpose of this study is to investigate how triptolide inhibits NF-${\kappa}B$-dependent IL-8 gene transcription in lung epithelial cells and to pilot the potential for the clinical application of triptolide in inflammatory lung diseases. Methods : A549 cells were used and triptolide was provided from Pharmagenesis Company (Palo Alto, CA). In order to examine NF-${\kappa}B$-dependent IL-8 transcriptional activity, we established stable A549 IL-8-NF-${\kappa}B$-luc. cells and performed luciferase assays. IL-8 gene expression was measured by RT-PCR and ELISA. A Western blot was done for the study of $I{\kappa}B{\alpha}$ degradation and an electromobility shift assay was done to analyze NF-${\kappa}B$ DNA binding. p65 specific transactivation was analyzed by a cotransfection study using a Gal4-p65 fusion protein expression system. To investigate the involvement of transcriptional coactivators, we perfomed a transfection study with CBP and SRC-1 expression vectors. Results : We observed that triptolide significantly suppresses NF-${\kappa}B$-dependent IL-8 transcriptional activity induced by IL-$1{\beta}$ and PMA. RT-PCR showed that triptolide represses both IL-$1{\beta}$ and PMA-induced IL-8 mRNA expression and ELISA confirmed this triptolide-mediated IL-8 suppression at the protein level. However, triptolide did not affect $I{\kappa}B{\alpha}$ degradation and NF-$_{\kappa}B$ DNA binding. In a p65-specific transactivation study, triptolide significantly suppressed Gal4-p65T Al and Gal4-p65T A2 activity suggesting that triptolide inhibits NF-${\kappa}B$ activation by inhibiting p65 transactivation. However, this triptolide-mediated inhibition of p65 transactivation was not rescued by the overexpression of CBP or SRC-1, thereby excluding the role of transcriptional coactivators. Conclusions : Triptolide is a new compound that inhibits NF-${\kappa}B$-dependent IL-8 transcriptional activation by inhibiting p65 transactivation, but not by an $I{\kappa}B{\alpha}$-dependent mechanism. This suggests that triptolide may have a therapeutic potential for inflammatory lung diseases.

• Journal of the Korean Mathematical Society
• /
• v.53 no.2
• /
• pp.315-329
• /
• 2016

In the setting of continuous logic, we study atomless probability spaces and atomless random variable structures. We characterize ${\kappa}$-saturated atomless probability spaces and ${\kappa}$-saturated atomless random variable structures for every infinite cardinal ${\kappa}$. Moreover, ${\kappa}$-saturated and strongly ${\kappa}$-homogeneous atomless probability spaces and ${\kappa}$-saturated and strongly ${\kappa}$-homogeneous atomless random variable structures are characterized for every infinite cardinal ${\kappa}$. For atomless probability spaces, we prove that ${\aleph}_1$-saturation is equivalent to Hoover-Keisler saturation. For atomless random variable structures whose underlying probability spaces are Hoover-Keisler saturated, we prove several equivalent conditions.

• YAKHAK HOEJI
• /
• v.54 no.3
• /
• pp.200-204
• /
• 2010

Nuclear factor-${\kappa}B$ (NF-${\kappa}B$) plays critical roles in physiological and pathological processes such as immune function, cellular growth, homeostasis, apoptosis, and inflammation. As part of our ongoing efforts to develop novel NF-${\kappa}B$ inhibitory agents, we reported that KL-1156 (6-hydroxy-7-methoxychroman-2-carboxylic acid phenylamide) exhibited potent inhibitory activity of NF-${\kappa}B$. For further structure-activity relationship, a series of 7-aryloxy-chroman-2-carboxylamide derivatives were synthesized to explore their inhibitory activities of NF-${\kappa}B$.

• Journal of Microbiology and Biotechnology
• /
• v.19 no.6
• /
• pp.556-559
• /
• 2009

Compounds extracted from Platycodon grandiflorum were evaluated for an activation effect on nuclear factor-kappa B (NF-${\kappa}B$). In its active state, NF-${\kappa}B$ turns on the expression of genes related to cell proliferation or death. NF-${\kappa}B$ activators promote growth of neuron cells and can be used to control neurodegenerative diseases. The biological activity of P. grandiflorum extracts toward NF-${\kappa}B$ had not yet been studied. Although the biological activity of several compounds extracted from P. grandiflorum was evaluated, only three exhibited any significant activation effect on NF-${\kappa}B$.

• 한국전산유체공학회:학술대회논문집
• /
• 2003.08a
• /
• pp.158-163
• /
• 2003

This paper assesses the two-equation turbulence models available in a commercial code, FLUENT, for heat transfer in a turbulent heated pipe flow. In case of flow under $Re_D=10,000$, Standard $\kappa-\epsilon$ and Realizable $\kappa-\epsilon$ models overpredict the Nusselt number about $20\%$ compared with the experimental correlation, and RNG $\kappa-\epsilon$ model overpredicts about $30\%$ when the two-layer zonal method is employed. When wall function method is adopted, all $\kappa-\epsilon$ models show better predictions. Standard $\kappa-\omega$ and SST $\kappa-\omega$ models have the dependency on the first grid point ($0.3). As Reynolds number becomes high, the predictions of all $\kappa-\epsilon$ and $\kappa-\omega$ models are in a good agreement with the experimental correlation.

• Journal of Pharmaceutical Investigation
• /
• v.23 no.4
• /
• pp.213-216
• /
• 1993

${\kappa}-Carrageenan$, an anionic polysaccharide, was employed in tablet formulations and its function as a drug release sustaining agent was investigated. Tablets composed of ${\kappa}-carrageenan$ and hydroxypropyl methylcellulose were fabricated by using direct compression method. Lactose and sodium alginate were utilized as controls for ${\kappa}-carrageenan$. Drug release experiments performed at pHs 1.2 and 7.4 revealed that ${\kappa}-carrageenan$ retains pH-dependent sustained release effects due to its anionic characteristics. Also, the ionic interaction between ${\kappa}-carrageenan$ and drugs exerted significant affects on drug release kinetics. ${\kappa}-Carrageenan$ was found out to be a useful additive for sustained release tablet formulations.

• Molecules and Cells
• /
• v.37 no.3
• /
• pp.189-195
• /
• 2014

The NF-${\kappa}B$ pathway transcriptionally controls a large set of target genes that play important roles in cell survival, inflammation, and immune responses. While many studies showed anti-tumorigenic and pro-survival role of NF-${\kappa}B$ in cancer cells, recent findings postulate that NF-${\kappa}B$ participates in a senescence-associated cytokine response, thereby suggesting a tumor restraining role of NF-${\kappa}B$. In this review, we discuss implications of the NF-${\kappa}B$ signaling pathway in cancer. Particularly, we emphasize the connection of NF-${\kappa}B$ with cellular senescence as a response to chemotherapy, and furthermore, present examples how distinct oncogenic network contexts surrounding NF-${\kappa}B$ produce fundamentally different treatment outcomes in aggressive B-cell lymphomas as an example.

• Korean Journal of Microbiology
• /
• v.54 no.3
• /
• pp.208-213
• /
• 2018

Activation of nuclear factor kappa B ($NF{\kappa}B$) leads to the inflammatory process. During this $NF{\kappa}B$-dependent inflammation process, inducible nitric oxide synthase (iNOS) are expressed in the inflammatory cells. Our previous data indicated that a specific septapeptide (GVAWWMY) from the soybean extract fermented by Bacillus licheniformis B1 inhibited iNOS mRNA expression and NO production in cultured macrophage cells. Our further experiments revealed that treatment of same septapeptide resulted in inhibition of LPS-induced $NF{\kappa}B$ activation by reversing degradation of $I{\kappa}B{\alpha}$, an inhibitory protein for $NF{\kappa}B$. The molecular docking indicated that the septapeptide binds to $I{\kappa}B$ kinase ${\beta}$ ($IKK{\beta}$), and thus it can inhibit phosphorylation of $I{\kappa}B{\alpha}$. Supporting this, the binding site for the septapeptide has the highest affinity (-8.7 kcal/mol) and the site was located at the kinase domain (KD) of $IKK{\beta}$, which can significantly affect the kinase activity of $IKK{\beta}$.