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Choroidal Neovascularization Is Inhibited in Splenic-Denervated or Splenectomized Mice with a Concomitant Decrease in Intraocular Macrophage

PURPOSE: To determine the involvement of sympathetic activity in choroidal neovascularization (CNV) using laser-induced CNV in a mouse model. METHODS: We investigated changes in the proportions of intraocular lymphocytes, granulocytes, and three macrophage subtypes (Ly6C(hi), Ly6C(int), and Ly6C(lo)...

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Autores principales: Tan, Xue, Fujiu, Katsuhito, Manabe, Ichiro, Nishida, Junko, Yamagishi, Reiko, Terashima, Yuya, Matsushima, Kouji, Kaburaki, Toshikatsu, Nagai, Ryozo, Yanagi, Yasuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988653/
https://www.ncbi.nlm.nih.gov/pubmed/27532664
http://dx.doi.org/10.1371/journal.pone.0160985
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author Tan, Xue
Fujiu, Katsuhito
Manabe, Ichiro
Nishida, Junko
Yamagishi, Reiko
Terashima, Yuya
Matsushima, Kouji
Kaburaki, Toshikatsu
Nagai, Ryozo
Yanagi, Yasuo
author_facet Tan, Xue
Fujiu, Katsuhito
Manabe, Ichiro
Nishida, Junko
Yamagishi, Reiko
Terashima, Yuya
Matsushima, Kouji
Kaburaki, Toshikatsu
Nagai, Ryozo
Yanagi, Yasuo
author_sort Tan, Xue
collection PubMed
description PURPOSE: To determine the involvement of sympathetic activity in choroidal neovascularization (CNV) using laser-induced CNV in a mouse model. METHODS: We investigated changes in the proportions of intraocular lymphocytes, granulocytes, and three macrophage subtypes (Ly6C(hi), Ly6C(int), and Ly6C(lo)) after laser injury in mice using flow cytometry, and evaluated CNV lesion size in mice lacking inflammatory cells. Further, we evaluated the lesion size in mice administered the β3 receptor antagonist, splenic-denervated and splenectomized mice. We also assessed changes in the proportions of intraocular macrophages and peripheral blood monocytes in splenic-denervated and splenectomized mice. Lastly, lesion size was compared between splenic-denervated mice with or without adoptive transfer of macrophages following laser injury. After Ly5.1 mice spleen-derived Ly6C(hi) cells were transferred into Ly5.2 mice, the proportions of intraocular Ly5.1(+)Ly6C(hi) cells were compared. RESULTS: In WT mice, the proportion of CD4(+) T cells recruited into the eye increased progressively from day 3 to day 7 after laser injury, whereas, intraocular CD8(+) T cells did not change significantly. Proportions of B220(+) cells, granulocytes, and two subtypes of intraocular macrophages (Ly6C(hi) and Ly6C(lo)) peaked at day 3 following laser injury. In contrast, Ly6C(int/lo)CD64(+) subtype showed a significantly higher percentage at day 7 after laser injury. There were no differences in lesion size between CD4(–/–)or Rag2(–/–)mice and controls, whereas lesion size was significantly reduced in CCR2(−/−) mice and clodronate liposome-treated mice. CNV lesion area was significantly reduced in mice with β3 blocker treatment, splenic-denervated and splenectomized mice compared with controls. Intraocular Ly6C(hi) macrophages were also reduced by splenic denervation or splenectomy. Adoptive transfer of spleen-derived Ly6C(hi) cells increased the lesion size in splenic-denervated mice. Compared with controls, intraocular donor-derived Ly6C(hi) cells recruited into the eye were reduced in splenic-denervated and splenectomized mice. CONCLUSIONS: Although lymphocytes had little effect on CNV formation, Ly6C(hi) macrophages/monocytes exacerbated CNV in mice. Sympathetic activity might contribute to CNV via the recruitment of macrophages to the eye.
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spelling pubmed-49886532016-08-29 Choroidal Neovascularization Is Inhibited in Splenic-Denervated or Splenectomized Mice with a Concomitant Decrease in Intraocular Macrophage Tan, Xue Fujiu, Katsuhito Manabe, Ichiro Nishida, Junko Yamagishi, Reiko Terashima, Yuya Matsushima, Kouji Kaburaki, Toshikatsu Nagai, Ryozo Yanagi, Yasuo PLoS One Research Article PURPOSE: To determine the involvement of sympathetic activity in choroidal neovascularization (CNV) using laser-induced CNV in a mouse model. METHODS: We investigated changes in the proportions of intraocular lymphocytes, granulocytes, and three macrophage subtypes (Ly6C(hi), Ly6C(int), and Ly6C(lo)) after laser injury in mice using flow cytometry, and evaluated CNV lesion size in mice lacking inflammatory cells. Further, we evaluated the lesion size in mice administered the β3 receptor antagonist, splenic-denervated and splenectomized mice. We also assessed changes in the proportions of intraocular macrophages and peripheral blood monocytes in splenic-denervated and splenectomized mice. Lastly, lesion size was compared between splenic-denervated mice with or without adoptive transfer of macrophages following laser injury. After Ly5.1 mice spleen-derived Ly6C(hi) cells were transferred into Ly5.2 mice, the proportions of intraocular Ly5.1(+)Ly6C(hi) cells were compared. RESULTS: In WT mice, the proportion of CD4(+) T cells recruited into the eye increased progressively from day 3 to day 7 after laser injury, whereas, intraocular CD8(+) T cells did not change significantly. Proportions of B220(+) cells, granulocytes, and two subtypes of intraocular macrophages (Ly6C(hi) and Ly6C(lo)) peaked at day 3 following laser injury. In contrast, Ly6C(int/lo)CD64(+) subtype showed a significantly higher percentage at day 7 after laser injury. There were no differences in lesion size between CD4(–/–)or Rag2(–/–)mice and controls, whereas lesion size was significantly reduced in CCR2(−/−) mice and clodronate liposome-treated mice. CNV lesion area was significantly reduced in mice with β3 blocker treatment, splenic-denervated and splenectomized mice compared with controls. Intraocular Ly6C(hi) macrophages were also reduced by splenic denervation or splenectomy. Adoptive transfer of spleen-derived Ly6C(hi) cells increased the lesion size in splenic-denervated mice. Compared with controls, intraocular donor-derived Ly6C(hi) cells recruited into the eye were reduced in splenic-denervated and splenectomized mice. CONCLUSIONS: Although lymphocytes had little effect on CNV formation, Ly6C(hi) macrophages/monocytes exacerbated CNV in mice. Sympathetic activity might contribute to CNV via the recruitment of macrophages to the eye. Public Library of Science 2016-08-17 /pmc/articles/PMC4988653/ /pubmed/27532664 http://dx.doi.org/10.1371/journal.pone.0160985 Text en © 2016 Tan 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Tan, Xue
Fujiu, Katsuhito
Manabe, Ichiro
Nishida, Junko
Yamagishi, Reiko
Terashima, Yuya
Matsushima, Kouji
Kaburaki, Toshikatsu
Nagai, Ryozo
Yanagi, Yasuo
Choroidal Neovascularization Is Inhibited in Splenic-Denervated or Splenectomized Mice with a Concomitant Decrease in Intraocular Macrophage
title Choroidal Neovascularization Is Inhibited in Splenic-Denervated or Splenectomized Mice with a Concomitant Decrease in Intraocular Macrophage
title_full Choroidal Neovascularization Is Inhibited in Splenic-Denervated or Splenectomized Mice with a Concomitant Decrease in Intraocular Macrophage
title_fullStr Choroidal Neovascularization Is Inhibited in Splenic-Denervated or Splenectomized Mice with a Concomitant Decrease in Intraocular Macrophage
title_full_unstemmed Choroidal Neovascularization Is Inhibited in Splenic-Denervated or Splenectomized Mice with a Concomitant Decrease in Intraocular Macrophage
title_short Choroidal Neovascularization Is Inhibited in Splenic-Denervated or Splenectomized Mice with a Concomitant Decrease in Intraocular Macrophage
title_sort choroidal neovascularization is inhibited in splenic-denervated or splenectomized mice with a concomitant decrease in intraocular macrophage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988653/
https://www.ncbi.nlm.nih.gov/pubmed/27532664
http://dx.doi.org/10.1371/journal.pone.0160985
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