نتایج جستجو برای: p38 map kinase inhibitors

تعداد نتایج: 577103  

2017
Jonas Cicenas Egle Zalyte Arnas Rimkus Dalius Dapkus Remigijus Noreika Sigitas Urbonavicius

Mitogen-activated protein kinases (MAP kinases) are a family of kinases that regulates a range of biological processes implicated in the response to growth factors like latelet-derived growth factor (PDGF), epidermal growth factor (EGF), vascular endothelial growth factor (VEGF), and stress, such as ultraviolet irradiation, heat shock, and osmotic shock. The MAP kinase family consists of four m...

Journal: :Blood 1999
M Goebeler K Kilian R Gillitzer M Kunz T Yoshimura E B Bröcker U R Rapp S Ludwig

Monocyte chemoattractant protein-1 (MCP-1), a member of the C-C subfamily of chemokines, is important for the local recruitment of leukocytes to sites of inflammatory challenge. Here, we investigated endothelial signaling pathways involving members of the mitogen-activated protein (MAP) kinase superfamily and studied their role for MCP-1 expression in endothelium. We show that tumor necrosis fa...

Journal: :American journal of physiology. Endocrinology and metabolism 1999
Hidenori Kawamura Takanobu Otsuka Hiroyuki Matsuno Masayuki Niwa Nobuo Matsui Kanefusa Kato Toshihiko Uematsu Osamu Kozawa

We previously reported that endothelin-1 (ET-1) activates p42/p44 mitogen-activated protein (MAP) kinase in osteoblast-like MC3T3-E1 cells and consequently induces synthesis of interleukin-6. In the present study, we investigated the effect of ET-1 on the induction of heat shock protein 27 (HSP 27) in MC3T3-E1 cells. ET-1 time and dose dependently stimulated HSP 27 accumulation. ET-1 induced an...

2013
Rintaro Okoshi Chung-Li Shu Sayoko Ihara Yasuhisa Fukui

Heregulin (HRG) β1 signaling promotes scattering of MCF7 cells by inducing breakdown of adherens and tight junctions. Here, we show that stimulation with HRG-β1 causes the F-actin backbone of junctions to destabilize prior to the loss of adherent proteins and scattering of the cells. The adherent proteins dissociate and translocate from cell-cell junctions to the cytosol. Moreover, using inhibi...

Journal: :Current Biology 1998
Rachel Ben-Levy Steven Hooper Rebecca Wilson Hugh F. Paterson Christopher J. Marshall

BACKGROUND Mitogen-activated protein (MAP) kinases (or extracellular signal regulated kinases; Erks) and stress-activated protein (SAP) kinases mediate cellular responses to a wide variety of signals. In the Erk MAP kinase pathway, activation of MAP kinases takes place in the cytoplasm and the activated enzyme moves to the nucleus. This translocation to the nucleus is essential to MAP kinase si...

2002
Min Huang Yanhong Wang Matthew Collins Jing Jin Gu Beverly S. Mitchell Lee M. Graves Mary Ellen

Journal: :Biology 2023

Although microglia exist as a minor glial cell type in the normal state of brain, they increase number response to various disorders and insults. However, it remains unclear whether proliferate affected area, mechanism proliferation has long attracted attention researchers. We analyzed microglial mitosis using facial nerve transection model which blood–brain barrier is left unimpaired when nerv...

Journal: :Pharmacology Biochemistry and Behavior 2011
Thacyana T. Carvalho Tamires Flauzino Eliane S. Otaguiri Ana P. Batistela Ana C. Zarpelon Thiago M. Cunha Sérgio H. Ferreira Fernando Q. Cunha Waldiceu A. Verri

Granulocyte-colony stimulating factor (G-CSF) is a current pharmacological approach to increase peripheral neutrophil counts after anti-tumor therapies. Pain is most relevant side effect of G-CSF in healthy volunteers and cancer patients. Therefore, the mechanisms of G-CSF-induced hyperalgesia were investigated focusing on the role of spinal mitogen-activated protein (MAP) kinases ERK (extracel...

2006
Antonija Jurak Begonja Jörg Geiger Natalia Rukoyatkina Steffen Rauchfuss Stepan Gambaryan Ulrich Walter

p38 MAP kinase in human platelets is activated by platelet agonists including thrombin, thromboxane A2 (TxA2), ADP, and others. However, both upstream mechanisms of p38 MAP kinase activation, and their downstream sequelae, are presently controversial and essentially unclear. Certain studies report sequential activation of cGMP-dependent protein kinase (PKG) and p38/ERK pathways by platelet agon...

Journal: :The Journal of pharmacology and experimental therapeutics 2003
Min Huang Yanhong Wang Susan B Cogut Beverly S Mitchell Lee M Graves

Recently we reported that the pyridinylimidazole class of p38 mitogen-activated protein (MAP) kinase inhibitors potently inhibited the facilitated transport of nucleosides and nucleoside analogs in K562 cells. These compounds competed with the binding of nitrobenzylthioinosine (NBMPR) to K562 cells, consistent with inhibition of the NBMPR-sensitive equilibrative transporter (ENT1). In this stud...

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