Monitoring differentiation of human embryonic stem cells using real-time PCR
(2005) In Stem Cells 23(10). p.1460-1467- Abstract
- There is a general lack of rapid, sensitive, and quantitative methods for the detection of differentiating human embryonic stem cells (hESCs). Using light microscopy and immunohistochemistry, we observed that morphological changes of differentiating hESCs precede any major alterations in the expression of several commonly used hESC markers (SSEA-3, SSEA-4, TRA-1-60, TRA-1-81, Oct-4, and Nanog). In an attempt to quantify the changes during stochastic differentiation of hESCs, we developed a robust and sensitive multimarker quantitative real-time polymerase chain reaction (QPCR) method. To maximize the sensitivity of the method, we measured the expression of up- and downregulated genes before and after differentiation of the hESCs. Out of... (More)
- There is a general lack of rapid, sensitive, and quantitative methods for the detection of differentiating human embryonic stem cells (hESCs). Using light microscopy and immunohistochemistry, we observed that morphological changes of differentiating hESCs precede any major alterations in the expression of several commonly used hESC markers (SSEA-3, SSEA-4, TRA-1-60, TRA-1-81, Oct-4, and Nanog). In an attempt to quantify the changes during stochastic differentiation of hESCs, we developed a robust and sensitive multimarker quantitative real-time polymerase chain reaction (QPCR) method. To maximize the sensitivity of the method, we measured the expression of up- and downregulated genes before and after differentiation of the hESCs. Out of the 12 genes assayed, we found it clearly sufficient to determine the relative differentiation state of the cells by calculating a collective expression index based on the mRNA levels of Oct-4, Nanog, Cripto, and (x-fetoprotein. We evaluated the method using different hESC lines maintained in either feeder-dependent or feeder-free culture conditions. The QPCR method is very flexible, and by appropriately selecting reporter genes, the method can be designed for various applications. The combination of QPCR with hESC-based technologies opens novel avenues for high-throughput analysis of hESCs in, for example, pharmacological and cytotoxicity screening. STEM CELLS 2005;23:1460-1467. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/211310
- author
- Noaksson, K ; Zoric, N ; Zeng, XM ; Rao, MS ; Hyllner, J ; Semb, Henrik LU ; Kubista, M and Sartipy, P
- organization
- publishing date
- 2005
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- real-time polymerase chain, human embryonic stem cell, differentiation, gene expression, reaction
- in
- Stem Cells
- volume
- 23
- issue
- 10
- pages
- 1460 - 1467
- publisher
- Oxford University Press
- external identifiers
-
- wos:000233708700005
- scopus:28444485641
- ISSN
- 1549-4918
- DOI
- 10.1634/stemcells.2005-0093
- language
- English
- LU publication?
- yes
- id
- 707dff2e-2978-4204-b798-40bbb621e236 (old id 211310)
- date added to LUP
- 2016-04-01 16:51:29
- date last changed
- 2023-01-05 03:09:55
@article{707dff2e-2978-4204-b798-40bbb621e236,
abstract = {{There is a general lack of rapid, sensitive, and quantitative methods for the detection of differentiating human embryonic stem cells (hESCs). Using light microscopy and immunohistochemistry, we observed that morphological changes of differentiating hESCs precede any major alterations in the expression of several commonly used hESC markers (SSEA-3, SSEA-4, TRA-1-60, TRA-1-81, Oct-4, and Nanog). In an attempt to quantify the changes during stochastic differentiation of hESCs, we developed a robust and sensitive multimarker quantitative real-time polymerase chain reaction (QPCR) method. To maximize the sensitivity of the method, we measured the expression of up- and downregulated genes before and after differentiation of the hESCs. Out of the 12 genes assayed, we found it clearly sufficient to determine the relative differentiation state of the cells by calculating a collective expression index based on the mRNA levels of Oct-4, Nanog, Cripto, and (x-fetoprotein. We evaluated the method using different hESC lines maintained in either feeder-dependent or feeder-free culture conditions. The QPCR method is very flexible, and by appropriately selecting reporter genes, the method can be designed for various applications. The combination of QPCR with hESC-based technologies opens novel avenues for high-throughput analysis of hESCs in, for example, pharmacological and cytotoxicity screening. STEM CELLS 2005;23:1460-1467.}},
author = {{Noaksson, K and Zoric, N and Zeng, XM and Rao, MS and Hyllner, J and Semb, Henrik and Kubista, M and Sartipy, P}},
issn = {{1549-4918}},
keywords = {{real-time polymerase chain; human embryonic stem cell; differentiation; gene expression; reaction}},
language = {{eng}},
number = {{10}},
pages = {{1460--1467}},
publisher = {{Oxford University Press}},
series = {{Stem Cells}},
title = {{Monitoring differentiation of human embryonic stem cells using real-time PCR}},
url = {{http://dx.doi.org/10.1634/stemcells.2005-0093}},
doi = {{10.1634/stemcells.2005-0093}},
volume = {{23}},
year = {{2005}},
}