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Retinal Ganglion Cell Loss Is Accompanied by Antibody Depositions and Increased Levels of Microglia after Immunization with Retinal Antigens

BACKGROUND: Antibodies against retinal and optic nerve antigens are detectable in glaucoma patients. Recent studies using a model of experimental autoimmune glaucoma demonstrated that immunization with certain ocular antigens causes an immun-mediated retinal ganglion cell loss in rats. METHODOLOGY/P...

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Autores principales: Joachim, Stephanie C., Gramlich, Oliver W., Laspas, Panagiotis, Schmid, Heiko, Beck, Sabine, von Pein, Harald D., Dick, H. Burkhard, Pfeiffer, Norbert, Grus, Franz H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406064/
https://www.ncbi.nlm.nih.gov/pubmed/22848388
http://dx.doi.org/10.1371/journal.pone.0040616
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author Joachim, Stephanie C.
Gramlich, Oliver W.
Laspas, Panagiotis
Schmid, Heiko
Beck, Sabine
von Pein, Harald D.
Dick, H. Burkhard
Pfeiffer, Norbert
Grus, Franz H.
author_facet Joachim, Stephanie C.
Gramlich, Oliver W.
Laspas, Panagiotis
Schmid, Heiko
Beck, Sabine
von Pein, Harald D.
Dick, H. Burkhard
Pfeiffer, Norbert
Grus, Franz H.
author_sort Joachim, Stephanie C.
collection PubMed
description BACKGROUND: Antibodies against retinal and optic nerve antigens are detectable in glaucoma patients. Recent studies using a model of experimental autoimmune glaucoma demonstrated that immunization with certain ocular antigens causes an immun-mediated retinal ganglion cell loss in rats. METHODOLOGY/PRINCIPAL FINDINGS: Rats immunized with a retinal ganglion cell layer homogenate (RGA) had a reduced retinal ganglion cell density on retinal flatmounts (p = 0.007) and a lower number of Brn3(+)retinal ganglion cells (p = 0.0001) after six weeks. The autoreactive antibody development against retina and optic nerve was examined throughout the study. The levels of autoreactive antibodies continuously increased up to 6 weeks (retina: p = 0.004; optic nerve: p = 0.000003). Additionally, antibody deposits were detected in the retina (p = 0.02). After 6 weeks a reactive gliosis (GFAP density: RGA: 174.7±41.9; CO: 137.6±36.8, p = 0.0006; %GFAP(+) area: RGA: 8.5±3.4; CO: 5.9±3.6, p = 0.006) as well as elevated level of Iba1(+) microglia cells (p = 0.003) was observed in retinas of RGA animals. CONCLUSIONS/SIGNIFICANCE: Our findings suggest that these antibodies play a substantial role in mechanisms leading to retinal ganglion cell death. This seems to lead to glia cell activation as well as the invasion of microglia, which might be associated with debris clearance.
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spelling pubmed-34060642012-07-30 Retinal Ganglion Cell Loss Is Accompanied by Antibody Depositions and Increased Levels of Microglia after Immunization with Retinal Antigens Joachim, Stephanie C. Gramlich, Oliver W. Laspas, Panagiotis Schmid, Heiko Beck, Sabine von Pein, Harald D. Dick, H. Burkhard Pfeiffer, Norbert Grus, Franz H. PLoS One Research Article BACKGROUND: Antibodies against retinal and optic nerve antigens are detectable in glaucoma patients. Recent studies using a model of experimental autoimmune glaucoma demonstrated that immunization with certain ocular antigens causes an immun-mediated retinal ganglion cell loss in rats. METHODOLOGY/PRINCIPAL FINDINGS: Rats immunized with a retinal ganglion cell layer homogenate (RGA) had a reduced retinal ganglion cell density on retinal flatmounts (p = 0.007) and a lower number of Brn3(+)retinal ganglion cells (p = 0.0001) after six weeks. The autoreactive antibody development against retina and optic nerve was examined throughout the study. The levels of autoreactive antibodies continuously increased up to 6 weeks (retina: p = 0.004; optic nerve: p = 0.000003). Additionally, antibody deposits were detected in the retina (p = 0.02). After 6 weeks a reactive gliosis (GFAP density: RGA: 174.7±41.9; CO: 137.6±36.8, p = 0.0006; %GFAP(+) area: RGA: 8.5±3.4; CO: 5.9±3.6, p = 0.006) as well as elevated level of Iba1(+) microglia cells (p = 0.003) was observed in retinas of RGA animals. CONCLUSIONS/SIGNIFICANCE: Our findings suggest that these antibodies play a substantial role in mechanisms leading to retinal ganglion cell death. This seems to lead to glia cell activation as well as the invasion of microglia, which might be associated with debris clearance. Public Library of Science 2012-07-26 /pmc/articles/PMC3406064/ /pubmed/22848388 http://dx.doi.org/10.1371/journal.pone.0040616 Text en © 2012 Joachim et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Joachim, Stephanie C.
Gramlich, Oliver W.
Laspas, Panagiotis
Schmid, Heiko
Beck, Sabine
von Pein, Harald D.
Dick, H. Burkhard
Pfeiffer, Norbert
Grus, Franz H.
Retinal Ganglion Cell Loss Is Accompanied by Antibody Depositions and Increased Levels of Microglia after Immunization with Retinal Antigens
title Retinal Ganglion Cell Loss Is Accompanied by Antibody Depositions and Increased Levels of Microglia after Immunization with Retinal Antigens
title_full Retinal Ganglion Cell Loss Is Accompanied by Antibody Depositions and Increased Levels of Microglia after Immunization with Retinal Antigens
title_fullStr Retinal Ganglion Cell Loss Is Accompanied by Antibody Depositions and Increased Levels of Microglia after Immunization with Retinal Antigens
title_full_unstemmed Retinal Ganglion Cell Loss Is Accompanied by Antibody Depositions and Increased Levels of Microglia after Immunization with Retinal Antigens
title_short Retinal Ganglion Cell Loss Is Accompanied by Antibody Depositions and Increased Levels of Microglia after Immunization with Retinal Antigens
title_sort retinal ganglion cell loss is accompanied by antibody depositions and increased levels of microglia after immunization with retinal antigens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406064/
https://www.ncbi.nlm.nih.gov/pubmed/22848388
http://dx.doi.org/10.1371/journal.pone.0040616
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