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Bone Marrow Transplantation Transfers Age-Related Susceptibility to Neovascular Remodeling in Murine Laser-Induced Choroidal Neovascularization
Author(s) -
Diego G. EspinosaHeidmann,
Goldis Malek,
Priyatham S. Mettu,
Alejandro Caicedo,
Peter Saloupis,
Sarah Gach,
Askia K. Dun,
Peng Hu,
Maria-Grazia Spiga,
Scott W. Cousins
Publication year - 2013
Publication title -
investigative ophthalmology and visual science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.935
H-Index - 218
eISSN - 1552-5783
pISSN - 0146-0404
DOI - 10.1167/iovs.13-12546
Subject(s) - bone marrow , pathology , choroidal neovascularization , neovascularization , mesenchymal stem cell , medicine , transplantation , fibrosis , cd31 , macular degeneration , immunohistochemistry , biology , angiogenesis , cancer research , ophthalmology
Neovascular remodeling (NVR), the progression of small capillaries into large-caliber arterioles with perivascular fibrosis, represents a major therapeutic challenge in neovascular age-related macular degeneration (AMD). Neovascular remodeling occurs after laser-induced choroidal neovascularization (CNV) in aged but not young mice. Additionally, bone marrow-derived cells, including macrophages, endothelial precursor cells, and mesenchymal precursor cells, contribute to CNV severity. In this study, we investigated the impact of aged bone marrow transplantation (BMT) on the degree of fibrosis, size, and vascular morphology of CNV lesions in a mouse model of laser-induced CNV.

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