Abstract
• Aim: To establish a culture method of Long Evans neonate rat retinal microglia cells(RMGs) in vitro. • Methods: Mixed glial cells of Long Evans rats (postnatal <3d) were cultured for 10-12 days, then RMGs were purified by shaking in 37°C swing bed and identified by specific microglia marker IB-4 and CD11b, and cell surface of RMGs were observed by Scanning EM. • Results: Purity of RMGs were 94.5% and 95.8% by cell immunochemistry identification of IB-4 and CD11b, cell surface showed spinous processes of RMGs, contrasting the smooth surfaces of macrophages. • Conclusion: Based on these data, a method is presented that proposes to use the microglial cell to effectively deliver therapeutic compounds to retinal disease.
Original language | English |
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Pages (from-to) | 1039-1041 |
Number of pages | 3 |
Journal | International Journal of Ophthalmology |
Volume | 6 |
Issue number | 5 |
Publication status | Published - Oct 2006 |
Externally published | Yes |
Keywords
- Cell culture
- Long Evans rats
- Retinal microglial cell