ED 27. Separation, culture and identification of SD rat corpus cavernosal endothelial cells
Erectile Dysfunction

ED 27. Separation, culture and identification of SD rat corpus cavernosal endothelial cells

Bin Zhang1, Jun Chen1, Cheng-Liang Sun2, Zheng Chen1, Heng-Jun Xiao3, Tao Qi1, Xiao-Ming Li1

1Department of Infertility and Sexual Medicine, the Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China; 2Department of Urology, Renmin Hospital, Hubei University of Medicine, Hubei 442000, China; 3Department of Urology, the Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China


To investigate the methods of separation, culture and identification of Sprague Dawley (SD) rat corpus cavernosal vascular endothelial cells (CCECs). Cavernosal tissues were isolated from male SD rats. Enzymatic digestion was applied to separate CCECs. Purified cells were obtained using immunomagnetic beads and flow cytometric cell sorting, and sub-cultured in EMG-2 medium. The growth curve of CCECs was measured by MTT assay. The cells were identified by von Willebrand factor (vWF) using immunofluorescence, and the positive percentage of vWF expression was detected by flow cytometry. The monomorphic cobblestone-like cells were observed by microscopy. High purification was obtained using immunomagnetic beads. After 2 days of incubation, cells entered the logarithmic growth phase, and reached a plateau on the fifth day. The von Willebrand factor expression in cytoplasm was positive. The purity of cells was 95.8%, which was tested by flow cytometry. SD rat CCECs can be separated and cultured successfully by the method of enzymatic digestion, immunomagnetic beads and flow cytometric cell sorting.

Key words

Rats; cavernosal tissues; endothelial cells; primary cell culture; immunomagnetic beads

DOI: 10.3978/j.issn.2223-4683.2012.s091

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