Detection and purification of cultured rat retinal Müller cell by flow cytometer
10.3760/cma.j.issn.2095-0160.2011.02.006
- VernacularTitle:利用流式细胞仪分选纯化大鼠视网膜Müller细胞
- Author:
Min, GONG
;
Bo-lin, XIE
;
Shu-qing, LI
;
Fan, LI
- Publication Type:Journal Article
- Keywords:
Müller cell;
Cell culture;
Flow cytometer
- From:
Chinese Journal of Experimental Ophthalmology
2011;29(2):121-124
- CountryChina
- Language:Chinese
-
Abstract:
Background Establising the culture model of Müller cells for obtaining the highly putified target cells is essential for the study about the physiology and pathology of retinal Müller cells. The exsiting purifing method for culturing Müller cells is dissatisfactory. Objective This study was to establish a method to obtain high purifing Müller cells. Methods The retina from 5 clean newborn SD rats were isolated and digested by 0. 01% trypsin and cultured in DMEM containing 10% fetal bovine serum. The cellular suspension was then prepared,and the target cells were screened using flow cytometry based on the size and the quantity of cells. Cultured and passaged cells were identified by transmission electron microscope and light microscope. Immunocytochemistry was used to detecte the expression of GFAP in cultured cells for the determination of type and purity of the cells. Results The cells showed the similar shape to retinal Müller cells after primarily culture with the large volume, and some small other types of cells could been seen. The growth of cells was quickly 3 weeks later. The fibroblasts were removed using sticking-wall by steps,and neurons were eliminated following passage. Aboundent of cellular organs were seen under the transmission electron microscope. The positive response rate of the cells for CFAP was 100%. Conclution Flow cytometry offer a rapid and feasible approach for purifying Muller cell and it builds the foundation for further study about Müller cells.
