• Title/Summary/Keyword: strongly ${\kappa}$-sequential

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STRONG VERSIONS OF κ-FRÉCHET AND κ-NET SPACES

  • CHO, MYUNG HYUN;KIM, JUNHUI;MOON, MI AE
    • Honam Mathematical Journal
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    • v.37 no.4
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    • pp.549-557
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    • 2015
  • We introduce strongly ${\kappa}$-$Fr{\acute{e}}chet$ and strongly ${\kappa}$-sequential spaces which are stronger than ${\kappa}$-$Fr{\acute{e}}chet$ and ${\kappa}$-net spaces respectively. For convenience, we use the terminology "${\kappa}$-sequential" instead of "${\kappa}$-net space", introduced by R.E. Hodel in [5]. And we study some properties and topological operations on such spaces. We also define strictly ${\kappa}$-$Fr{\acute{e}}chet$ and strictly ${\kappa}$-sequential spaces which are more stronger than strongly ${\kappa}$-$Fr{\acute{e}}chet$ and strongly ${\kappa}$-sequential spaces respectively.

ROLE OF NF${\kappa}B$ IN TOLL-LIKE RECEPTOR 9-MEDIATED MATRIX METALLOPROTEINASE-9 EXPRESSION (Toll-like receptor 9-매개에 의한 matrix metalloproteinase-9 발현에서 NF${\kappa}B$의 역할)

  • Lee, Sang-Hoon;Chin, Byung-Rho;Baek, Suk-Hwan
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • v.33 no.6
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    • pp.636-642
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    • 2007
  • Background: CpG DNA plays an important role in immune cell function. This study examined whether the temporal control of toll-like receptor (TLR)9 by CpG DNA can regulate the expression of matrix metalloproteinase-9(MMP-9). Methods and materials: Macrophages were cultured in the presence of 10% FBS. For the various MMP genes analysis, RT-PCR and real-time PCR were performed. In addition, zymography assay performed for the MMP activity. The phosphorylation assay did for the ERK1/2 and NF${\kappa}B$ activation, and luciferase promoter assay was for the NF${\kappa}B$ activity. Results: CpG DNA induced the mRNA expression of MMP-2, MMP-9, and MMP-13, but not of MMP-7, MMP-8, and MMP-12, in a time-dependent manner. Especially, the mRNA expression of MMP-9 was strongly induced by CpG DNA using real-time RT-PCR. The TLR9 inhibitor, chloroquine, suppressed CpG DNA-induced MMP-9 expression and its activity. Moreover, CpG DNA induced the phosphorylation of ERK and the inhibition of ERK by U0126 suppressed CpG DNA-induced MMP-9 expression and its activity. CpG DNA stimulated $I{\kappa}B-{\alpha}$ degradation and luciferase activity. In addition, pretreatment of SN-50, the inhibitor of NF${\kappa}B$, strongly blocked the CpG DNA-induced MMP-9 expression and activity. Conclusion: These observations suggest that CpG DNA may play important roles in the activation of macrophages by regulating the production of MMP-9 via the sequential TLR9-ERK-NF${\kappa}B$ signaling pathway.

Numerical Simulation of Developing Turbulent Flow in a Circular Pipe of 180° Bend (원형 단면을 갖는 180° 굽은 곡관내 발달하는 난류유동에 관한 수치해석)

  • Myong Hyon-Kook
    • Transactions of the Korean Society of Mechanical Engineers B
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    • v.30 no.10 s.253
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    • pp.966-972
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    • 2006
  • A numerical simulation is performed fur developing turbulent flow in a strongly curved 180 deg pipe and its downstream tangent by a new solution code(PowerCFD) which adopts an unstructured cell-centered method. The governing equations are discretized as the full elliptic from of the equations of motion. Three typical two-equation turbulence models of low-Reynolds-number form are used to approximate the turbulent stress field. Solutions fur both streamwise and circumferential velocity components are compared with the experimental data by Azzola et at.(1986). The ${\kappa}-{\omega}$ model by Wilcox(1988) is found to give better prediction performance than the other two. Predicted secondary velocities and streamwise velocity component contours at sequential longitudinal stations are also presented in order to enable a detailed description of the complete flow. It is also found that, in the bend both mean streamwise and secondary velocities never achieve a fully-developed state and the code is capable of producing very well the complex nature of steady flow in a strongly curved pipe.