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[Human lens epithelial cells culture in vitro]
1Zhongshan Ophthalmic Center, Sun Yat-sen University of Medical Sciences, Guangzhou 510060, China.
Purpose:
To provide a simple and rapid procedure to culture human len epithelial cells in vitro.
Methods:
Specimens of capsule lentils were isolated from lens by microscissors. They were cut into small segments and then directly implanted into basks(culture bottles). The tissue pieces were cultured in a incubation at 37 degrees C with PR1640 until attached cells reached confluence. The len epithelium were passaged by tropism.
Results:
Len epithelial cells usually appeared after 4 days in incubation. The cells growed rapidly in a way of attachments.
Conclusion:
Len epithelial cells were easily cultured with our method. The procedure is simple, rapid and highly successful.