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10.3389/fphys.2016.00387 http://scihub22266oqcxt.onion/10.3389/fphys.2016.00387 C5006658!5006658!27630579     free     free     free       Front+Physiol 2016 ; 7 (ä): ä Nephropedia Template TP {{tp|p=27630579|t=2016. Essential Role of Lyn in Fibrosis |pdf=|usr=}}{{27630579}} gab.com Text Essential Role of Lyn in Fibrosis JO: Front Physiol http://www.kidney.de/pget.php?&tw=1&pmid=27630579 #FOAvip Fibrotic disorders involve replacement of normal parenchyma with myofibroblasts, which deposit connective tissue, leading to obliteration of the function of the underlying organ. The treatment options are inadequate and reflect the fact that signaling targets in myofibroblasts are unknown. Here we identify the hyperactive Lyn signaling in myofibroblasts of patients with chronic pancreatitis-induced fibrosis. Lyn activation coexpress with markers of activated myofibroblasts, and is increased ~11-fold in chronic pancreatitis compared to normal tissue. Inhibition of Lyn with siRNA or INNO-406 leads to the substantial decrease of migration and proliferation of human chronic pancreatitis myofibroblasts in vitro, while leaving migration and proliferation of normal myofibroblasts only slightly affected. Furthermore, inhibition of Lyn prevents synthesis of procollagen and collagen in myofibroblasts in a mouse model of chronic pancreatitis-induced fibrosis. We conclude that Lyn, as a positive regulator of myofibroblast migration, proliferation, and collagen production, is a key target for preventing fibrosis. Twit Text FOAVip Essential Role of Lyn in Fibrosis ????Front Physiol http://www.kidney.de/pget.php?&tw=1&pmid=27630579 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27630579 #FOAvip English Wikipedia <ref>{{Cite pmid|27630579}}</ref> Essential Role of Lyn in Fibrosis #MMPMID27630579 Pham H; Birtolo C; Chheda C; Yang W; Rodriguez MD; Liu ST; Gugliotta G; Lewis MS; Cirulli V; Pandol SJ; Ptasznik A Front Physiol 2016[]; 7 (ä): ä PMID27630579show ga Fibrotic disorders involve replacement of normal parenchyma with myofibroblasts, which deposit connective tissue, leading to obliteration of the function of the underlying organ. The treatment options are inadequate and reflect the fact that signaling targets in myofibroblasts are unknown. Here we identify the hyperactive Lyn signaling in myofibroblasts of patients with chronic pancreatitis-induced fibrosis. Lyn activation coexpress with markers of activated myofibroblasts, and is increased ~11-fold in chronic pancreatitis compared to normal tissue. Inhibition of Lyn with siRNA or INNO-406 leads to the substantial decrease of migration and proliferation of human chronic pancreatitis myofibroblasts in vitro, while leaving migration and proliferation of normal myofibroblasts only slightly affected. Furthermore, inhibition of Lyn prevents synthesis of procollagen and collagen in myofibroblasts in a mouse model of chronic pancreatitis-induced fibrosis. We conclude that Lyn, as a positive regulator of myofibroblast migration, proliferation, and collagen production, is a key target for preventing fibrosis. äEssential Role of Lyn in Fibrosis (epmc).pdf DeepDyve Pubget Overpricing