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10.1167/iovs.18-24133 http://scihub22266oqcxt.onion/10.1167/iovs.18-24133 C6040236!6040236!30025090     free     free     free Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Invest+Ophthalmol+Vis+Sci 2018 ; 59 (8): 3405-15 Nephropedia Template TP {{tp|p=30025090|t=2018. Retinal Basal Laminar Deposits in Complement fH/fP Mouse Model of Dense Deposit Disease |pdf=|usr=}}{{30025090}} gab.com Text Retinal Basal Laminar Deposits in Complement fH/fP Mouse Model of Dense Deposit Disease JO: Invest Ophthalmol Vis Sci http://www.kidney.de/pget.php?&tw=1&pmid=30025090 #FOAvip Purpose: Dense deposit disease (DDD) is caused by dysregulation of the alternative pathway of the complement cascade and characterized by electron-dense deposits in the kidney glomerular basement membrane (GBM) and drusen in Bruch's membrane (BrM). Complement factor H (fH) and factor properdin (fP) regulate complement activation; fH inhibits alternative pathway (AP) activation, whereas fP promotes it. We report pathologic changes in eyes of an fH and fP double-mutant mouse, which we previously showed have dense deposits in the GBM and early mortality from nephropathy. Methods: fHm/m, fP?/?, and fHm/m/fP?/? mice were generated on a C57BL/6?129J background. Fundus imaging at 8 weeks of age was followed by analysis via light and electron microscopy. Retinal function was assessed by electroretinography (ERG). Complement levels and localization were tested by immunohistochemistry and ELISA. Retinas of fHm/m/fP?/? mice treated with intraperitoneal injections of an anti-C5 antibody were compared to those of age- and genotype-matched mice injected with an isotype control antibody. Results: fHm/m/fP?/? mice suffered early-onset retinal hypopigmented spots detected using in vivo retinal photography, and histologic examination showed basal laminar deposits (BLamD), degeneration of the photoreceptors, and RPE vacuolization. ERG showed diminished retinal function. The anti-C5 antibody was retina-protective. Conclusions: This unique mouse represents a new model of complement-mediated rapid-onset DDD, and could be useful in exploring the pathologic changes associated with BLamD in age-related macular degeneration. Twit Text FOAVip Retinal Basal Laminar Deposits in Complement fH/fP Mouse Model of Dense Deposit Disease ????Invest Ophthalmol Vis Sci http://www.kidney.de/pget.php?&tw=1&pmid=30025090 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=30025090 #FOAvip English Wikipedia <ref>{{Cite pmid|30025090}}</ref> Retinal Basal Laminar Deposits in Complement fH/fP Mouse Model of Dense Deposit Disease #MMPMID30025090 Song D; Mohammed I; Bhuyan R; Miwa T; Williams AL; Gullipalli D; Sato S; Song Y; Dunaief JL; Song WC Invest Ophthalmol Vis Sci 2018[Jul]; 59 (8): 3405-15 PMID30025090show ga Purpose: Dense deposit disease (DDD) is caused by dysregulation of the alternative pathway of the complement cascade and characterized by electron-dense deposits in the kidney glomerular basement membrane (GBM) and drusen in Bruch's membrane (BrM). Complement factor H (fH) and factor properdin (fP) regulate complement activation; fH inhibits alternative pathway (AP) activation, whereas fP promotes it. We report pathologic changes in eyes of an fH and fP double-mutant mouse, which we previously showed have dense deposits in the GBM and early mortality from nephropathy. Methods: fHm/m, fP?/?, and fHm/m/fP?/? mice were generated on a C57BL/6?129J background. Fundus imaging at 8 weeks of age was followed by analysis via light and electron microscopy. Retinal function was assessed by electroretinography (ERG). Complement levels and localization were tested by immunohistochemistry and ELISA. Retinas of fHm/m/fP?/? mice treated with intraperitoneal injections of an anti-C5 antibody were compared to those of age- and genotype-matched mice injected with an isotype control antibody. Results: fHm/m/fP?/? mice suffered early-onset retinal hypopigmented spots detected using in vivo retinal photography, and histologic examination showed basal laminar deposits (BLamD), degeneration of the photoreceptors, and RPE vacuolization. ERG showed diminished retinal function. The anti-C5 antibody was retina-protective. Conclusions: This unique mouse represents a new model of complement-mediated rapid-onset DDD, and could be useful in exploring the pathologic changes associated with BLamD in age-related macular degeneration. äRetinal Basal Laminar Deposits in Complement fH/fP Mouse Model of Dens(epmc).pdf DeepDyve Pubget Overpricing