Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText. Kick-your-searchterm to multiple Engines kick-your-query now !>

A dictionary by aggregated review articles of nephrology, medicine and the life sciences Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

10.1002/iid3.114 http://scihub22266oqcxt.onion/10.1002/iid3.114 C5004285!5004285!27621813     free     free     free Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Immun+Inflamm+Dis 2016 ; 4 (3): 300-14 Nephropedia Template TP {{tp|p=27621813|t=2016. Early infiltration of p40IL12+CCR7+CD11b+ cells is critical for fibrosis development |pdf=|usr=}}{{27621813}} gab.com Text Early infiltration of p40IL12+CCR7+CD11b+ cells is critical for fibrosis development JO: Immun Inflamm Dis http://www.kidney.de/pget.php?&tw=1&pmid=27621813 #FOAvip Introduction: Macrophages are heterogeneous and thus can be correlated with distinct tissue outcomes after injury. Conflicting data have indicated that the M2?related phenotype directly triggers fibrosis. Conversely, we hypothesize here that the inflammatory milieu provided by early infiltration of pro?inflammatory macrophages dictates tissue scarring after injury. Methods and Results: We first determined that tissue?localized macrophages exhibit a pro?inflammatory phenotype (p40IL12+CCR7+CD11b+) during the early phase of a chronic injury model, in contrast to a pro?resolving phenotype (Arg1+IL10+CD206+CD11b+) at a later stage. Then, we evaluated the effects of injecting macrophages differentiated in vitro in the presence of IFN??+?LPS or IL4?+?IL13 or non?differentiated macrophages (hereafter, M0) on promoting inflammation and progression of chronic injury in macrophage?depleted mice. In addition to enhancing the expression of pro?inflammatory cytokines, the injection of M (IFN??+?LPS), but not M (IL4?+?IL13) or M0, accentuated fibrosis while augmenting levels of anti?inflammatory molecules, increasing collagen deposition and impairing organ function. We observed a similar profile after injection of sorted CCR7+CD11b+ cells and a more pronounced effect of M (IFN??+?LPS) cells originated from Stat6?/? mice. The injection of M (IFN??+?LPS) cells was associated with the up?regulation of inflammation? and fibrosis?related proteins (Thbs1, Mmp7, Mmp8, and Mmp13). Conclusions: Our results suggest that pro?inflammatory macrophages promote microenvironmental changes that may lead to fibrogenesis by inducing an inflammatory milieu that alters a network of extracellular?related genes, culminating in tissue fibrosis. Twit Text FOAVip Early infiltration of p40IL12+CCR7+CD11b+ cells is critical for fibrosis development ????Immun Inflamm Dis http://www.kidney.de/pget.php?&tw=1&pmid=27621813 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27621813 #FOAvip English Wikipedia <ref>{{Cite pmid|27621813}}</ref> Early infiltration of p40IL12+CCR7+CD11b+ cells is critical for fibrosis development #MMPMID27621813 Braga TT; Correa?Costa M; Azevedo H; Silva RC; Cruz MC; Almeida MES; Hiyane MI; Moreira?Filho CA; Santos MF; Perez KR; Cuccovia IM; Camara NOS Immun Inflamm Dis 2016[Sep]; 4 (3): 300-14 PMID27621813show ga Introduction: Macrophages are heterogeneous and thus can be correlated with distinct tissue outcomes after injury. Conflicting data have indicated that the M2?related phenotype directly triggers fibrosis. Conversely, we hypothesize here that the inflammatory milieu provided by early infiltration of pro?inflammatory macrophages dictates tissue scarring after injury. Methods and Results: We first determined that tissue?localized macrophages exhibit a pro?inflammatory phenotype (p40IL12+CCR7+CD11b+) during the early phase of a chronic injury model, in contrast to a pro?resolving phenotype (Arg1+IL10+CD206+CD11b+) at a later stage. Then, we evaluated the effects of injecting macrophages differentiated in vitro in the presence of IFN??+?LPS or IL4?+?IL13 or non?differentiated macrophages (hereafter, M0) on promoting inflammation and progression of chronic injury in macrophage?depleted mice. In addition to enhancing the expression of pro?inflammatory cytokines, the injection of M (IFN??+?LPS), but not M (IL4?+?IL13) or M0, accentuated fibrosis while augmenting levels of anti?inflammatory molecules, increasing collagen deposition and impairing organ function. We observed a similar profile after injection of sorted CCR7+CD11b+ cells and a more pronounced effect of M (IFN??+?LPS) cells originated from Stat6?/? mice. The injection of M (IFN??+?LPS) cells was associated with the up?regulation of inflammation? and fibrosis?related proteins (Thbs1, Mmp7, Mmp8, and Mmp13). Conclusions: Our results suggest that pro?inflammatory macrophages promote microenvironmental changes that may lead to fibrogenesis by inducing an inflammatory milieu that alters a network of extracellular?related genes, culminating in tissue fibrosis. äEarly infiltration of p40IL12+CCR7+CD11b+ cells is critical for fibros(epmc).pdf DeepDyve Pubget Overpricing