Efficient Cultivation Conditions for Human Limbal Epithelial Cells.
10.3346/jkms.2008.23.5.864
- Author:
Mee Kum KIM
1
;
Jae Lim LEE
;
Joo Youn OH
;
Mi Sun SHIN
;
Kyeong Seon SHIN
;
Won Ryang WEE
;
Jin Hak LEE
;
Ki Sook PARK
;
Young Sook SON
Author Information
1. Department of Ophthalmology, Seoul National University College of Medicine, Seoul, Korea. wrwee@snu.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Amniotic Membrane;
Cornea;
Limbal Epithelial Cell;
CK12;
p63
- MeSH:
3T3 Cells;
Animals;
Cell Culture Techniques/*instrumentation/*methods;
Cells, Cultured;
Cytological Techniques;
DNA Primers/chemistry;
Epithelial Cells/*metabolism;
Humans;
Immunohistochemistry/methods;
Keratin-12/metabolism;
Mice;
Models, Biological;
Phosphoproteins/metabolism;
Reverse Transcriptase Polymerase Chain Reaction;
Stem Cells/cytology;
Trans-Activators/metabolism
- From:Journal of Korean Medical Science
2008;23(5):864-869
- CountryRepublic of Korea
- Language:English
-
Abstract:
To compare the stem niche in different culture conditions of limbal epithelial cells, the suspended human limbal epithelial cells (HLECs) were seeded on the 3T3-pretreated plates and the other suspended cells were plated on amniotic membranes (AMs) which were either cryo-preserved or freeze-dried. All were cultured for 10 to 12 days. Reverse transcription-polymerase chain reaction (RT-PCR) for ATP-binding casette, subfamily G, member 2 (ABCG2), p63, cytokeratin 12, and connexin 43 were performed in cultivated HLECs and their expression levels were compared. The mRNA expression of all markers examined showed no statistically significant differences between the cells on cryo-preserved and on freeze-dried AM. The expression of p63 and cytokeratin 12 in cultivated cells on AMs were significantly lower than those in 3T3-cocultured cells on RT-PCR and immunofluorescent staining. Cultivated HLECs on AMs showed reduced proliferation and differentiation while maintaining stem-property regardless of the preservative method of AM.
