Microcarrier Culture for Efficient Expansion and Osteogenic Differentiation of Human Fetal Mesenchymal Stem Cells
Identifieur interne : 000308 ( Main/Exploration ); précédent : 000307; suivant : 000309Microcarrier Culture for Efficient Expansion and Osteogenic Differentiation of Human Fetal Mesenchymal Stem Cells
Auteurs : Tony Kwang-Poh Goh ; Zhi-Yong Zhang ; Allen Kuan-Liang Chen ; Shaul Reuveny ; Mahesh Choolani ; Jerry Kok Yen Chan ; Steve Kah-Weng OhSource :
- BioResearch Open Access [ 2164-7844 ] ; 2013.
Abstract
Stirred microcarrier (MC) culture has been suggested as the method of choice for supplying large volumes of mesenchymal stem cells (MSCs) for bone tissue engineering. In this study, we show that in addition to the improvement in cell expansion capacity, MSCs propagated and harvested from MC culture also demonstrate higher osteogenic potency when differentiated
Url:
DOI: 10.1089/biores.2013.0001
PubMed: 23593561
PubMed Central: 3620494
Affiliations:
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Microcarrier Culture for Efficient Expansion and Osteogenic Differentiation of Human Fetal Mesenchymal Stem Cells</title>
<author><name sortKey="Goh, Tony Kwang Poh" sort="Goh, Tony Kwang Poh" uniqKey="Goh T" first="Tony Kwang-Poh" last="Goh">Tony Kwang-Poh Goh</name>
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<author><name sortKey="Zhang, Zhi Yong" sort="Zhang, Zhi Yong" uniqKey="Zhang Z" first="Zhi-Yong" last="Zhang">Zhi-Yong Zhang</name>
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<author><name sortKey="Chen, Allen Kuan Liang" sort="Chen, Allen Kuan Liang" uniqKey="Chen A" first="Allen Kuan-Liang" last="Chen">Allen Kuan-Liang Chen</name>
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<author><name sortKey="Reuveny, Shaul" sort="Reuveny, Shaul" uniqKey="Reuveny S" first="Shaul" last="Reuveny">Shaul Reuveny</name>
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<author><name sortKey="Choolani, Mahesh" sort="Choolani, Mahesh" uniqKey="Choolani M" first="Mahesh" last="Choolani">Mahesh Choolani</name>
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<author><name sortKey="Chan, Jerry Kok Yen" sort="Chan, Jerry Kok Yen" uniqKey="Chan J" first="Jerry Kok Yen" last="Chan">Jerry Kok Yen Chan</name>
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<author><name sortKey="Oh, Steve Kah Weng" sort="Oh, Steve Kah Weng" uniqKey="Oh S" first="Steve Kah-Weng" last="Oh">Steve Kah-Weng Oh</name>
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<series><title level="j">BioResearch Open Access</title>
<idno type="ISSN">2164-7844</idno>
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<front><div type="abstract" xml:lang="en"><title>Abstract</title>
<p>Stirred microcarrier (MC) culture has been suggested as the method of choice for supplying large volumes of mesenchymal stem cells (MSCs) for bone tissue engineering. In this study, we show that in addition to the improvement in cell expansion capacity, MSCs propagated and harvested from MC culture also demonstrate higher osteogenic potency when differentiated <italic>in vivo</italic>
or <italic>in vitro</italic>
in three-dimensional (3D) scaffold cultures as compared with traditional monolayer (MNL) cultures. Cytodex 3 microcarrier-expanded human fetal MSC (hfMSC) cultures (MC-hfMSCs) achieved 12- to 16-fold expansion efficiency (6×10<sup>5</sup>
–8×10<sup>5</sup>
cells/mL) compared to 4- to 6-fold (1.2×10<sup>5</sup>
–1.8×10<sup>5</sup>
cells/mL) achieved by traditional MNL-expanded hfMSC culture (MNL-hfMSCs; <italic>p</italic>
<0.05). Both MC-hfMSCs and MNL-hfMSCs maintained similar colony-forming capacity, doubling times, and immunophenotype postexpansion. However, when differentiated under <italic>in vitro</italic>
two-dimensional (2D) osteogenic conditions, MC-hfMSCs exhibited a 45-fold reduction in alkaline phosphatase level and a 37.5% decrease in calcium deposition compared with MNL-hfMSCs (<italic>p</italic>
<0.05). Surprisingly, when MC-hfMSCs and MNL-hfMSCs were seeded on 3D macroporous scaffold culture or subcutaneously implanted into nonobese diabetic/severe combined immunodeficient mice, MC-hfMSCs deposited 63.5% (<italic>p</italic>
<0.05) more calcium and formed 47.2% (<italic>p</italic>
<0.05) more bone volume, respectively. These results suggest that the mode of hfMSC growth in the expansion phase affects the osteogenic potential of hfMSCs differently in various differentiation platforms. In conclusion, MC cultures are advantageous over MNL cultures in bone tissue engineering because MC-hfMSCs have improved cell expansion capacity and exhibit higher osteogenic potential than MNL-hfMSCs when seeded <italic>in vitro</italic>
into 3D scaffolds or implanted <italic>in vivo</italic>
.</p>
</div>
</front>
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<tree><noCountry><name sortKey="Chan, Jerry Kok Yen" sort="Chan, Jerry Kok Yen" uniqKey="Chan J" first="Jerry Kok Yen" last="Chan">Jerry Kok Yen Chan</name>
<name sortKey="Chen, Allen Kuan Liang" sort="Chen, Allen Kuan Liang" uniqKey="Chen A" first="Allen Kuan-Liang" last="Chen">Allen Kuan-Liang Chen</name>
<name sortKey="Choolani, Mahesh" sort="Choolani, Mahesh" uniqKey="Choolani M" first="Mahesh" last="Choolani">Mahesh Choolani</name>
<name sortKey="Goh, Tony Kwang Poh" sort="Goh, Tony Kwang Poh" uniqKey="Goh T" first="Tony Kwang-Poh" last="Goh">Tony Kwang-Poh Goh</name>
<name sortKey="Oh, Steve Kah Weng" sort="Oh, Steve Kah Weng" uniqKey="Oh S" first="Steve Kah-Weng" last="Oh">Steve Kah-Weng Oh</name>
<name sortKey="Reuveny, Shaul" sort="Reuveny, Shaul" uniqKey="Reuveny S" first="Shaul" last="Reuveny">Shaul Reuveny</name>
<name sortKey="Zhang, Zhi Yong" sort="Zhang, Zhi Yong" uniqKey="Zhang Z" first="Zhi-Yong" last="Zhang">Zhi-Yong Zhang</name>
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