Msx2 plays a critical role in lens epithelium cell cycle control
AIM: To investigate the effects of Msx2 on lens epithelium cell cycle, and evaluate the changes of the proliferation, apoptosis of lens epithelium cells. ·METHODS: Mice lens epithelium cells were cultured and transfected with pEGFP -Msx2 and control. Msx2 - deficient mice (Msx2 -/- ) lens tissue wer...
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Published in | International journal of ophthalmology Vol. 6; no. 3; pp. 276 - 279 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
China
International Journal of Ophthalmology Press
2013
Press of International Journal of Ophthalmology (IJO PRESS) |
Subjects | |
Online Access | Get full text |
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Summary: | AIM: To investigate the effects of Msx2 on lens epithelium cell cycle, and evaluate the changes of the proliferation, apoptosis of lens epithelium cells. ·METHODS: Mice lens epithelium cells were cultured and transfected with pEGFP -Msx2 and control. Msx2 - deficient mice (Msx2 -/- ) lens tissue were isolated. Lens tissue and transfected cells were prepared for mRNA extraction using Trizol reagent. CyclinD1 and Prox1 expression were evaluated by real -time RT -PCR. BrdU incorporation and apoptosis rate were investigated by immunofluorescence and flow cytometry analysis. ·RESULTS: After transfected with pEGFP-Msx2, lens epithelium cells failed to incorporate BrdU and anti - phospho-histone-3 immunofluorescence failed to detect cell nuclei which GFP were positive. Msx2 over expression resulted in increasing apoptosis rate in lens epithelium cells. CyclinD1 and Prox1 expression increased significantly in Msx2 knockout mice by real - time RT -PCR quantization and CyclinD1 expression decreased significantly in Msx2 overexpressed cell. · CONCLUSION: Msx2 has the effect of inhibiting proliferation and differentiation, triggering apoptosis on mice lens epithelium cells. |
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Bibliography: | Jiang-Yue Zhao 1 , Feng-Feng Zhuang 2 , Hong-Yan Wang 3 , Di Wu 1 , Jin-Song Zhang 11 Eye Hospital of China Medical University; Department of Ophthalmology, the 4 th Affiliated Hospital of China Medical University; Provincial Key Laboratory of Lens Research, Shenyang 110005, Liaoning Province, China 2 Department of Ophthalmology and Doheny Eye Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA 3 Department of General Surgery, People’s Hospital of Liaoning Province, Shenyang 110005, Liaoning Province, China ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2222-3959 2227-4898 |
DOI: | 10.3980/j.issn.2222-3959.2013.03.04 |