Non-invasive characterization of the adipogenic differentiation of human bone marrow-derived mesenchymal stromal cells by HS-SPME/GC-MS

Dong Kyu Lee, Tacghee Yi, Kyung Eun Park, Hyun Joo Lee, Yun Kyoung Cho, Seul Ji Lee, Jeongmi Lee, Jeong Hill Park, Mi Young Lee, Sun U. Song, Sung Won Kwon

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

A non-invasive method to characterize human mesenchymal stromal cells during adipogenic differentiation was developed for the first time. Seven fatty acid methyl esters (FAMEs), including methyl laurate, methyl myristate, methyl palmitate, methyl linoleate, methyl oleate, methyl elaidate and methyl stearate, were used for characterizing adipogenic differentiation using headspace solid-phase microextraction (HS-SPME) which is a very simple and non-invasive method for the extraction of volatile compounds. Glassware was used for culturing mesenchymal stromal cells rather than the common plasticware to minimize contamination by volatile impurities. The optimal SPME fiber was selected by comparing diverse fibers containing two pure liquid polymers (PDMS and PA) and two porous solids (PDMS/DVB and CAR/PDMS). Using optimized procedures, we discovered that seven FAMEs were only detected in adipogenic differentiated mesenchymal stromal cells and not in the mesenchymal stromal cells before differentiation. These data could support the quality control of clinical mesenchymal stromal cell culture in the pharmaceutical industry in addition to the development of many clinical applications using mesenchymal stromal cells.

Original languageEnglish (US)
Article number6550
JournalScientific Reports
Volume4
DOIs
StatePublished - 2014

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Solid Phase Microextraction
Mesenchymal Stromal Cells
Bone Marrow
Esters
Fatty Acids
Stearates
Myristic Acid
Drug Industry
Quality Control
Cell Differentiation
Polymers
Cell Culture Techniques

ASJC Scopus subject areas

  • General

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Non-invasive characterization of the adipogenic differentiation of human bone marrow-derived mesenchymal stromal cells by HS-SPME/GC-MS. / Lee, Dong Kyu; Yi, Tacghee; Park, Kyung Eun; Lee, Hyun Joo; Cho, Yun Kyoung; Lee, Seul Ji; Lee, Jeongmi; Park, Jeong Hill; Lee, Mi Young; Song, Sun U.; Kwon, Sung Won.

In: Scientific Reports, Vol. 4, 6550, 2014.

Research output: Contribution to journalArticle

Lee, DK, Yi, T, Park, KE, Lee, HJ, Cho, YK, Lee, SJ, Lee, J, Park, JH, Lee, MY, Song, SU & Kwon, SW 2014, 'Non-invasive characterization of the adipogenic differentiation of human bone marrow-derived mesenchymal stromal cells by HS-SPME/GC-MS', Scientific Reports, vol. 4, 6550. https://doi.org/10.1038/srep06550
Lee, Dong Kyu ; Yi, Tacghee ; Park, Kyung Eun ; Lee, Hyun Joo ; Cho, Yun Kyoung ; Lee, Seul Ji ; Lee, Jeongmi ; Park, Jeong Hill ; Lee, Mi Young ; Song, Sun U. ; Kwon, Sung Won. / Non-invasive characterization of the adipogenic differentiation of human bone marrow-derived mesenchymal stromal cells by HS-SPME/GC-MS. In: Scientific Reports. 2014 ; Vol. 4.
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abstract = "A non-invasive method to characterize human mesenchymal stromal cells during adipogenic differentiation was developed for the first time. Seven fatty acid methyl esters (FAMEs), including methyl laurate, methyl myristate, methyl palmitate, methyl linoleate, methyl oleate, methyl elaidate and methyl stearate, were used for characterizing adipogenic differentiation using headspace solid-phase microextraction (HS-SPME) which is a very simple and non-invasive method for the extraction of volatile compounds. Glassware was used for culturing mesenchymal stromal cells rather than the common plasticware to minimize contamination by volatile impurities. The optimal SPME fiber was selected by comparing diverse fibers containing two pure liquid polymers (PDMS and PA) and two porous solids (PDMS/DVB and CAR/PDMS). Using optimized procedures, we discovered that seven FAMEs were only detected in adipogenic differentiated mesenchymal stromal cells and not in the mesenchymal stromal cells before differentiation. These data could support the quality control of clinical mesenchymal stromal cell culture in the pharmaceutical industry in addition to the development of many clinical applications using mesenchymal stromal cells.",
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AU - Cho, Yun Kyoung

AU - Lee, Seul Ji

AU - Lee, Jeongmi

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AU - Song, Sun U.

AU - Kwon, Sung Won

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