[HTML][HTML] Choroidal neovascularization enhanced by Chlamydia pneumoniae via Toll-like receptor 2 in the retinal pigment epithelium
T Fujimoto, KH Sonoda, K Hijioka… - … & visual science, 2010 - tvst.arvojournals.org
T Fujimoto, KH Sonoda, K Hijioka, K Sato, A Takeda, E Hasegawa, Y Oshima, T Ishibashi
Investigative ophthalmology & visual science, 2010•tvst.arvojournals.orgPurpose.: Choroidal neovascularization (CNV) is directly related to visual loss in persons
with age-related macular degeneration (AMD) and other macular disorders. Chlamydia
pneumoniae, a prokaryotic pathogen that causes chronic inflammation, is recognized as a
risk factor for cardiovascular diseases. In this study, the authors investigated the association
between C. pneumoniae infection and AMD using a laser-induced CNV model in mice.
Methods.: C57BL/6 mice, myeloid differentiation factor (MyD) 88 knockout (KO) mice, Toll …
with age-related macular degeneration (AMD) and other macular disorders. Chlamydia
pneumoniae, a prokaryotic pathogen that causes chronic inflammation, is recognized as a
risk factor for cardiovascular diseases. In this study, the authors investigated the association
between C. pneumoniae infection and AMD using a laser-induced CNV model in mice.
Methods.: C57BL/6 mice, myeloid differentiation factor (MyD) 88 knockout (KO) mice, Toll …
Abstract
Purpose.: Choroidal neovascularization (CNV) is directly related to visual loss in persons with age-related macular degeneration (AMD) and other macular disorders. Chlamydia pneumoniae, a prokaryotic pathogen that causes chronic inflammation, is recognized as a risk factor for cardiovascular diseases. In this study, the authors investigated the association between C. pneumoniae infection and AMD using a laser-induced CNV model in mice.
Methods.: C57BL/6 mice, myeloid differentiation factor (MyD) 88 knockout (KO) mice, Toll-like receptor (TLR) 2 KO mice, and TLR4 KO mice were used. Experimental CNV was induced by rupturing the Bruch's membrane by laser photocoagulation (PC). Seven days after PC, the eyes were enucleated and the areas of CNV were measured in choroidal flat mounts. Cytokine gene expression by quantitative real-time PCR in the primary cultured retinal pigment epithelium (RPE) cells was also examined.
Results.: Vitreous injection of the C. pneumoniae antigen increased the size of CNV. Although lipopolysaccharide stimulation can induce multiple cytokines, cultured mouse RPE cells from C57BL/6 mice expressed IL-6 and VEGF, but not TNF-α mRNA, in response to C. pneumoniae antigen. RPE cells from either MyD88 KO mice or TLR2 KO mice did not respond to the C. pneumoniae antigen. TLR2 KO mice did not augment the size increase of experimental CNV by C. pneumoniae antigen in vivo.
Conclusions.: C. pneumoniae can trigger inflammatory responses in the eye and promote experimental CNV in a TLR2-dependent manner. These data provide experimental evidence to imply persistent C. pneumoniae infection is a risk factor for AMD.
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