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10.1038/jcbfm.2013.236 http://scihub22266oqcxt.onion/10.1038/jcbfm.2013.236 C3982080!3982080!24398937     free     free     free Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Cereb+Blood+Flow+Metab 2014 ; 34 (4): 621-9 Nephropedia Template TP {{tp|p=24398937|t=2014. Pyroptotic neuronal cell death mediated by the AIM2 inflammasome |pdf=|usr=}}{{24398937}} gab.com Text Pyroptotic neuronal cell death mediated by the AIM2 inflammasome JO: J Cereb Blood Flow Metab http://www.kidney.de/pget.php?&tw=1&pmid=24398937 #FOAvip The central nervous system (CNS) is an active participant in the innate immune response to infection and injury. In these studies, we show embryonic cortical neurons express a functional, deoxyribonucleic acid (DNA)-responsive, absent in melanoma 2 (AIM2) inflammasome that activates caspase-1. Neurons undergo pyroptosis, a proinflammatory cell death mechanism characterized by the following: (a) oligomerization of apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC); (b) caspase-1 dependency; (c) formation of discrete pores in the plasma membrane; and (d) release of the inflammatory cytokine interleukin-1? (IL-1?). Probenecid and Brilliant Blue FCF, inhibitors of the pannexin1 channel, prevent AIM2 inflammasome-mediated cell death, identifying pannexin1 as a cell death effector during pyroptosis and probenecid as a novel pyroptosis inhibitor. Furthermore, we show activation of the AIM2 inflammasome in neurons by cerebrospinal fluid (CSF) from traumatic brain injury (TBI) patients and oligomerization of ASC. These findings suggest neuronal pyroptosis is an important cell death mechanism during CNS infection and injury that may be attenuated by probenecid. Twit Text FOAVip Pyroptotic neuronal cell death mediated by the AIM2 inflammasome ????J Cereb Blood Flow Metab http://www.kidney.de/pget.php?&tw=1&pmid=24398937 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24398937 #FOAvip English Wikipedia <ref>{{Cite pmid|24398937}}</ref> Pyroptotic neuronal cell death mediated by the AIM2 inflammasome #MMPMID24398937 Adamczak SE; de Rivero Vaccari JP; Dale G; Brand FJ; Nonner D; Bullock M; Dahl GP; Dietrich WD; Keane RW J Cereb Blood Flow Metab 2014[Apr]; 34 (4): 621-9 PMID24398937show ga The central nervous system (CNS) is an active participant in the innate immune response to infection and injury. In these studies, we show embryonic cortical neurons express a functional, deoxyribonucleic acid (DNA)-responsive, absent in melanoma 2 (AIM2) inflammasome that activates caspase-1. Neurons undergo pyroptosis, a proinflammatory cell death mechanism characterized by the following: (a) oligomerization of apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC); (b) caspase-1 dependency; (c) formation of discrete pores in the plasma membrane; and (d) release of the inflammatory cytokine interleukin-1? (IL-1?). Probenecid and Brilliant Blue FCF, inhibitors of the pannexin1 channel, prevent AIM2 inflammasome-mediated cell death, identifying pannexin1 as a cell death effector during pyroptosis and probenecid as a novel pyroptosis inhibitor. Furthermore, we show activation of the AIM2 inflammasome in neurons by cerebrospinal fluid (CSF) from traumatic brain injury (TBI) patients and oligomerization of ASC. These findings suggest neuronal pyroptosis is an important cell death mechanism during CNS infection and injury that may be attenuated by probenecid. äPyroptotic neuronal cell death mediated by the AIM2 inflammasome (epmc).pdf DeepDyve Pubget Overpricing