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Vol. 219, No. 3, 2005   

Free Abstract     Article (Fulltext)     Article (PDF 323 KB)     

Original Paper

Comparison of the Proliferation and Differentiation Ability between Adult Rat Retinal Stem Cells and Cerebral Cortex-Derived Neural Stem Cells
I-Hsien Liua, Shih-Jen Chena, Hung-Hai Kud, Chung-Lan Kaoc, Fu-Ting Tsaia, Wen-Ming Hsua, Chih-Wen Loa, Yao-Haur Kuoe, Cheng-Deng Kuob, Chen-hsen Leeb, Shih-Hwa Chioua, b,e

Departments of
aOphthalmology,
bMedical Research and Education and
cPhysical Medicine and Rehabilitation, Taipei Veterans General Hospital and National Yang-Ming University,
dInstitute of Anatomy and Cell Biology, National Yang-Ming University, and
eNational Research Institute of Chinese Medicine, Taipei, Taiwan, ROC

Address of Corresponding Author

Ophthalmologica 2005;219:171-176 (DOI: 10.1159/000085250)


 goto top of page Key Words

  • Retinal stem cells
  • Cerebral-cortex-derived neural stem cells
  • Photoreceptors
  • Transforming growth factor beta type III

 goto top of page Abstract

Recent studies have demonstrated that retinal stem cells (RSCs) and stem cells of the central nervous system both exhibited the abilities of self-renewal, proliferation and differentiation into multilineage. In the present study, we compared the proliferation and differentiation abilities between RSCs and cerebral corticex-derived neural stem cells (CNSCs) of adult rats. Stem cells isolated from pigmented ciliary margins of eyes and cerebral cortical tissues of adult rats were cultured in 96-well plates that contained serum-free medium with epidermal growth factor (EGF) and basic fibroblast growth factor (bFGF). In contrast to RSCs, which stopped proliferating after the 8th week, the total cell count of neurospheres in CNSCs increased twofold at the 5th week and more than fourfold at the 10th week after in vitro culture. In contrast, RSCs stopped proliferating after 8 weeks of culture. After adding 2% fetal calf serum and withdrawing EGF and bFGF from the culture medium, the percentages of nestin-positive cells(20.6 ± 2.7%), microtubule-associated-protein-2-positive neurons (33.2 ± 3.9%) and glial-fibrillary-acidic-protein-positive glial cells(51.3 ± 6.2%) in the differentiated CNSCs were significantly higher than those in the differentiated RSCs (10.2 ± 1.9, 22.3 ± 1.3 and 44.6 ± 5.1%, respectively; p < 0.05). We also found that the combination of transforming growth factor beta type III with retinoic acid played an important role in the induction of CNSCs to differentiate into opsin-positive cells. Our data demonstrated that CNSCs displayed a higher ability of proliferation and retinal lineage. This report also offers an alternative protocol of cell reproduction for producing retinal cells.

Copyright © 2005 S. Karger AG, Basel


 goto top of page Author Contacts

Shih-Hwa Chiou, MD, PhD
Department of Ophthalmology, Taipei Veterans General Hospital
No. 201, Section 2, Shih-Pai Road
Taipei 11217, Taiwan (ROC)
Tel. +886 2 28757325, Fax +886 2 28720959, E-Mail shchiou@vghtpe.gov.tw


 goto top of page Article Information

Received: March 11, 2004
Accepted after revision: June 24, 2004
Number of Print Pages : 6
Number of Figures : 3, Number of Tables : 1, Number of References : 18

 
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