نتایج جستجو برای: larg practices

تعداد نتایج: 181028  

2012
Wei-Chiao Chiu Jyh-ming Juang Shen-nan Chang Cho-kai Wu Chia-ti Tsai Chuen-den Tseng Yung-zu Tseng Ming-Jai Su Fu-tien Chiang

PURPOSE Studies to explore angiotensin II (Ang II) and its downstream signaling pathways via Rho guanine nucleotide exchange factors (RhoGEFs) and RhoA signaling are crucial to understanding the mechanisms of smooth muscle contraction leading to hypertension. This study aimed to investigate the Ang II-induced expression of RhoGEFs in vascular smooth muscle cells (VSMCs) of spontaneously hyperte...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2010
Matt D Medlin Dean P Staus Adi D Dubash Joan M Taylor Christopher P Mack

OBJECTIVE The goals of this study were to identify the signaling pathway by which sphingosine 1-phosphate (S1P) activates RhoA in smooth muscle cells (SMC) and to evaluate the contribution of this pathway to the regulation of SMC phenotype. METHODS AND RESULTS Using a combination of receptor-specific agonists and antagonists we identified S1P receptor 2 (S1PR2) as the major S1P receptor subty...

Journal: :Neuron 2002
Jakub M. Swiercz Rohini Kuner Jürgen Behrens Stefan Offermanns

Plexins are widely expressed transmembrane proteins that, in the nervous system, mediate repulsive signals of semaphorins. However, the molecular nature of plexin-mediated signal transduction remains poorly understood. Here, we demonstrate that plexin-B family members associate through their C termini with the Rho guanine nucleotide exchange factors PDZ-RhoGEF and LARG. Activation of plexin-B1 ...

Journal: :Journalism Practice 2021

Given prevailing questions about the definition of news in a contemporary US media environment, present study analyzes audience views on news, exploring through in-depth interviews how 65 (larg...

2013
Yunfan Yang Lei Sun Tala Jinmin Gao Dengwen Li Jun Zhou Min Liu

Rho family guanosine triphosphatases (GTPases), such as RhoA, Cdc42, and Rac1, play a fundamental role in various cellular processes. The activation of Rho proteins is catalyzed by guanine nucleotide-exchange factors (GEFs), which promote the exchange of GDP for GTP. The precise mechanisms regulating the activation of Rho proteins are not fully understood. Herein, we demonstrate that RhoA activ...

Journal: :Molecular pharmacology 2006
Zhekang Ying Liming Jin Trenis Palmer R Clinton Webb

In vascular smooth muscle, stimulation of heterotrimeric G protein-coupled receptors (GPCRs) by various contractile agonists activates intracellular signaling molecules to result in an increase in cytosolic Ca2+ and the subsequent phosphorylation of myosin light chain (MLC) by Ca2+/calmodulin-dependent MLC kinase. In addition, a portion of agonist-induced contraction is partially mediated by th...

Journal: :Methods in molecular biology 2012
Xun Shang Yi Zheng

Rho GTPases have been implicated in diverse cellular functions and are potential therapeutic targets in inflammation, cancer, and neurologic diseases. Virtual screening of compounds that fit into surface grooves of RhoA known to be critical for guanine nucleotide exchange factor (GEF) interaction produced chemical candidates with minimized docking energy. Subsequent screening for inhibitory act...

Journal: :Molecular pharmacology 2004
Susumu Nakamura Barry Kreutz Shihori Tanabe Nobuchika Suzuki Tohru Kozasa

Heterotrimeric G proteins of the G12 family regulate the Rho GTPase through RhoGEFs that contain an amino-terminal regulator of G protein signaling (RGS) domain (RGS-RhoGEFs). Direct regulation of the activity of RGS-RhoGEFs p115 or leukemia-associated RhoGEF (LARG) by Galpha13 has previously been demonstrated. However, the precise biochemical mechanism by which Galpha13 stimulates the RhoGEF a...

Journal: :Genes & development 2007
Thomas M Kitzing Arul S Sahadevan Dominique T Brandt Helga Knieling Sebastian Hannemann Oliver T Fackler Jörg Grosshans Robert Grosse

The RhoA-effector Dia1 controls actin-dependent processes such as cytokinesis, SRF transcriptional activity, and cell motility. Dia1 polymerizes actin through its formin homology (FH) 2 domain. Here we show that Dia1 acts upstream of RhoA independently of its effects on actin assembly. Dia1 binds to the leukemia-associated Rho-GEF (LARG) through RhoA-dependent release of Dia1 autoinhibition. Th...

2013
Benjamin J Ritchie William C Smolski Ellyn R Montgomery Elizabeth S Fisher Tina Y Choi Calla M Olson Lori A Foster Thomas E Meigs

BACKGROUND Heterotrimeric guanine nucleotide binding proteins of the G12/13 subfamily, which includes the α-subunits Gα12 and Gα13, stimulate the monomeric G protein RhoA through interaction with a distinct subset of Rho-specific guanine nucleotide exchange factors (RhoGEFs). The structural features that mediate interaction between Gα13 and RhoGEFs have been examined in crystallographic studies...

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