Expression of OCT-4 in C-kit positive full term amniotic fluid cells by real-time PCR in extended culture / Nursuaidah Ramlan

The discovery of amniotic fluid stem (AFS) cells has initiated a new and very promising field in stem cell research. The unique characteristic of AFS cells can be seen from their differentiation potential where these cells are broadly multipotent to pluripotent, giving them a great potential in drug...

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Bibliographic Details
Main Author: Ramlan, Nursuaidah
Format: Thesis
Language:English
Published: 2014
Subjects:
Online Access:https://ir.uitm.edu.my/id/eprint/111011/1/111011.PDF
https://ir.uitm.edu.my/id/eprint/111011/
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Summary:The discovery of amniotic fluid stem (AFS) cells has initiated a new and very promising field in stem cell research. The unique characteristic of AFS cells can be seen from their differentiation potential where these cells are broadly multipotent to pluripotent, giving them a great potential in drug discovery. AFS cells that have been derived from full term pregnancy serves a better alternative compared to the midterm gestation as it is more accessible, less adverse effects and safer to the patients involved. Previous studies have reported that full-term AF c-kit positive cells are able to express the pluripotency marker, Oct-4. This study aims to investigate the stability of the full-term AF c-kit positive cells by examining the expression of Oct-4 in extended culture by qRT-PCR. The cells were first attached in a gelatin coated flask, with ES medium supplemented with LIF. Then, the RNA was extracted and synthesized into cDNA. The result demonstrated that the expression of Oct-4 in AF c-kit positive cells in passage 70 is weak. However, further troubleshooting needs to be carried out to validate the result. Based on the result, overall, the stability of the cells could be compromised in extended culture although further study needs to be carried out to validate the result. Therefore, low passage number is more recommended for studies using full-term AF c-kit positive cells.