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Retinal Explant of the Adult Mouse Retina as an Ex Vivo Model for Studying Retinal Neurovascular Diseases
Published on: December 9, 2022
Bone marrow-derived cells are differentially involved in pathological and physiological retinal angiogenesis in mice
He Zou1, Atsushi Otani, Akio Oishi
1Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto 606-8507, Japan.
Biochemical and Biophysical Research Communications
|December 17, 2009
Summary
Bone marrow cells are crucial for physiological retinal angiogenesis but not for pathological angiogenesis. This study clarifies their differential roles in retinal vessel formation and disease.
Area of Science:
- Ophthalmology
- Vascular Biology
- Cell Biology
Background:
- Bone marrow-derived cells are implicated in angiogenesis.
- Their specific roles in different types of angiogenesis, particularly in the retina, remain unclear.
Purpose of the Study:
- To investigate the involvement of bone marrow-derived cells in pathological and physiological retinal angiogenesis in mice.
- To determine if bone marrow-derived cells influence all forms of retinal angiogenesis.
Main Methods:
- Utilized the oxygen-induced retinopathy (OIR) model in newborn mice.
- Irradiated mice to deplete bone marrow-derived cells, with specific shielding protocols for different groups.
- Quantified pathological and physiological retinal angiogenesis on postnatal day 17.
Main Results:
- Irradiation led to leukocyte depletion but did not affect other cell types or body weight.
- Physiological angiogenesis was impaired in irradiated mice, evidenced by larger nonperfusion areas.
- Pathological angiogenesis, characterized by tuft-like structures, was unaffected or even enhanced in irradiated mice.
Conclusions:
- Bone marrow-derived cells play distinct roles in physiological versus pathological retinal angiogenesis.
- Functional bone marrow-derived cells are essential for physiological vessel formation but not for pathological angiogenesis.
- These findings offer insights into retinal angiogenic diseases and the contribution of bone marrow cells.

