Using organotypic cultures of the retina as a model for studying migratory activity of transplanted cells
- Authors: Semen ML1, Sergeev SA1, Saburina IN1, Kosheleva NV1, Semenova ML2, Sergeev SA2, Saburina IN3, Koscheleva NV4
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Affiliations:
- Lomonosov Moscow State University, Moscow
- Institute of General Pathology and Pathophysiology, Moscow
- Lomonosov Moscow State University, MoscowInstitute of General Pathology and Pathophysiology, Moscow
- Issue: Vol 5, No 2 (2010)
- Pages: 55-61
- Section: Articles
- URL: https://genescells.ru/2313-1829/article/view/121476
- DOI: https://doi.org/10.23868/gc121476
- ID: 121476
Cite item
Abstract
We used newborn rat neuroretina explantation culture (DMEM/F12 with 20ng/mlFGFandEGF, 7% FCS and antibiotics). After 10 days of cultivation retina pigment epithelium cells, MMSC and NSPC from the subventricular brain zone of C57BL/ B-TgCACTB-EGFP)/Osb/J GFP+ mice were transplanted into the cultured neuroretina/ explants. The immunohistochemical staining for [i-lll-tubulin and GFAP was carried out.
In our study significant differece in the survival capacity and migration ability of different cell types has been demonstrated, and morphological changes of transplanted cells were have been analyzed.
About the authors
M L Semen
S A Sergeev
I N Saburina
N V Kosheleva
M L Semenova
Lomonosov Moscow State University, MoscowLomonosov Moscow State University, Moscow
S A Sergeev
Lomonosov Moscow State University, MoscowLomonosov Moscow State University, Moscow
I N Saburina
Institute of General Pathology and Pathophysiology, MoscowInstitute of General Pathology and Pathophysiology, Moscow
N V Koscheleva
Lomonosov Moscow State University, MoscowInstitute of General Pathology and Pathophysiology, MoscowLomonosov Moscow State University, MoscowInstitute of General Pathology and Pathophysiology, Moscow
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