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ABSTRACT: Background and aim
Insufficient post-ischemic neovascularization is an initial key step in the pathogenesis of Oxygen-Induced Retinopathy (OIR). During neovascularization, pro-angiogenic cells (PACs) are mobilized from the bone marrow and integrate into ischemic tissues to promote angiogenesis. However, the modulation of PAC paracrine activity during OIR and the specific mechanisms involved remain to be explored. Because Tyrosine-protein phosphatase non-receptor type 9 (PTPN9) is reported to be a negative regulator of stem cell differentiation and angiogenesis signaling, we investigated its effect on PAC activity in the context of OIR.Methods and results
In a rat model of OIR, higher levels of PTPN9 in the retina and in bone marrow derived PACs are associated with retinal a
SUBMITTER: Desjarlais M
PROVIDER: S-EPMC8194284 | biostudies-literature | 2021
REPOSITORIES: biostudies-literature