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10.4161/auto.32170 http://scihub22266oqcxt.onion/10.4161/auto.32170 C4198371!4198371!25126735     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Autophagy 2014 ; 10 (10): 1866-7 Nephropedia Template TP {{tp|p=25126735|t=2014. A mitochondrial-associated link between an effector caspase and autophagic flux |pdf=|usr=}}{{25126735}} gab.com Text A mitochondrial-associated link between an effector caspase and autophagic flux JO: Autophagy http://www.kidney.de/pget.php?&tw=1&pmid=25126735 #FOAvip It has become evident that caspases function in nonapoptotic cellular processes in addition to the canonical role for caspases in apoptotic cell death. We recently demonstrated that the Drosophila effector caspase Dcp-1 localizes to the mitochondria and positively regulates starvation-induced autophagic flux during mid-oogenesis. Loss of Dcp-1 leads to elongation of the mitochondrial network, increased levels of the adenine nucleotide translocase sesB, increased ATP levels, and a reduction in autophagy. We found that sesB is a negative regulator of autophagic flux, and Dcp-1 interacts with sesB in a nonproteolytic manner to regulate its stability, uncovering a novel mechanism of mitochondrial associated, caspase-mediated regulation of autophagy in vivo. Twit Text FOAVip A mitochondrial-associated link between an effector caspase and autophagic flux ????Autophagy http://www.kidney.de/pget.php?&tw=1&pmid=25126735 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25126735 #FOAvip English Wikipedia <ref>{{Cite pmid|25126735}}</ref> A mitochondrial-associated link between an effector caspase and autophagic flux #MMPMID25126735 DeVorkin L; Gorski SM Autophagy 2014[Oct]; 10 (10): 1866-7 PMID25126735show ga It has become evident that caspases function in nonapoptotic cellular processes in addition to the canonical role for caspases in apoptotic cell death. We recently demonstrated that the Drosophila effector caspase Dcp-1 localizes to the mitochondria and positively regulates starvation-induced autophagic flux during mid-oogenesis. Loss of Dcp-1 leads to elongation of the mitochondrial network, increased levels of the adenine nucleotide translocase sesB, increased ATP levels, and a reduction in autophagy. We found that sesB is a negative regulator of autophagic flux, and Dcp-1 interacts with sesB in a nonproteolytic manner to regulate its stability, uncovering a novel mechanism of mitochondrial associated, caspase-mediated regulation of autophagy in vivo. äA mitochondrial-associated link between an effector caspase and autoph(epmc).pdf DeepDyve Pubget Overpricing