A three-layer over-the-cell multi-channel routing method for a new cell model

1995 ◽  
Author(s):  
Masahiro Tsuchiya ◽  
Tetsushi Koide ◽  
Shin'ichi Wakabayashi ◽  
Noriyosh Yoshida
Keyword(s):  
Cell Model ◽  
Channel Routing ◽  
Routing Method

scholarly journals On the restrictive channel thickness estimation

2007 ◽  
Vol 20 (3) ◽  
pp. 499-506
Author(s):  
Iskandar Karapetyan
Keyword(s):  
Positive Integer ◽  
Heuristic Algorithms ◽  
Clique Number ◽  
Directed Path ◽  
Channel Routing ◽  
Routing Problem ◽  
Thickness Estimation ◽  
Channel Thickness ◽  
Np Complete ◽  
Routing Method

Channel routing is an important phase of physical design of LSI and VLSI chips. The channel routing method was first proposed by Akihiro Hashimoto and James Stevens [1]. The method was extensively studied by many authors and applied to different technologies. At present there are known many effective heuristic algorithms for channel routing. A. LaPaugh [2] proved that the restrictive routing problem is NP-complete. In this paper we prove that for every positive integer k there is a restrictive channel C for which ?(C)>? (HG)+L(VG)+k, where ? (C) is the thickness of the channel, ?(HG) is clique number of the horizontal constraints graph HG and L(VG) is the length of the longest directed path in the vertical constraints graph VG.

Endogenous hydrogen sulfide sulfhydrates IKKβ at cysteine 179 to control pulmonary artery endothelial cell inflammation

2019 ◽  
Vol 133 (20) ◽  
pp. 2045-2059 ◽  
Author(s):  
Da Zhang ◽  
Xiuli Wang ◽  
Siyao Chen ◽  
Selena Chen ◽  
Wen Yu ◽  
...  
Keyword(s):  
Hydrogen Sulfide ◽  
Endothelial Cell ◽  
Pulmonary Artery ◽  
Cell Model ◽  
Site Directed Mutagenesis ◽  
Critical Event ◽  
Hypertensive Rats ◽  
Pulmonary Artery Endothelial Cell

Abstract Background: Pulmonary artery endothelial cell (PAEC) inflammation is a critical event in the development of pulmonary arterial hypertension (PAH). However, the pathogenesis of PAEC inflammation remains unclear. Methods: Purified recombinant human inhibitor of κB kinase subunit β (IKKβ) protein, human PAECs and monocrotaline-induced pulmonary hypertensive rats were employed in the study. Site-directed mutagenesis, gene knockdown or overexpression were conducted to manipulate the expression or activity of a target protein. Results: We showed that hydrogen sulfide (H2S) inhibited IKKβ activation in the cell model of human PAEC inflammation induced by monocrotaline pyrrole-stimulation or knockdown of cystathionine γ-lyase (CSE), an H2S generating enzyme. Mechanistically, H2S was proved to inhibit IKKβ activity directly via sulfhydrating IKKβ at cysteinyl residue 179 (C179) in purified recombinant IKKβ protein in vitro, whereas thiol reductant dithiothreitol (DTT) reversed H2S-induced IKKβ inactivation. Furthermore, to demonstrate the significance of IKKβ sulfhydration by H2S in the development of PAEC inflammation, we mutated C179 to serine (C179S) in IKKβ. In purified IKKβ protein, C179S mutation of IKKβ abolished H2S-induced IKKβ sulfhydration and the subsequent IKKβ inactivation. In human PAECs, C179S mutation of IKKβ blocked H2S-inhibited IKKβ activation and PAEC inflammatory response. In pulmonary hypertensive rats, C179S mutation of IKKβ abolished the inhibitory effect of H2S on IKKβ activation and pulmonary vascular inflammation and remodeling. Conclusion: Collectively, our in vivo and in vitro findings demonstrated, for the first time, that endogenous H2S directly inactivated IKKβ via sulfhydrating IKKβ at Cys179 to inhibit nuclear factor-κB (NF-κB) pathway activation and thereby control PAEC inflammation in PAH.

Discretionary channel routing

1988 ◽  
Vol 135 (2) ◽  
pp. 45
Author(s):  
H.W. Leong ◽  
C.L. Liu
Keyword(s):  
Channel Routing
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