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dc.contributor.authorSuteera Narakornsaken_US
dc.contributor.authorSirinda Aungsuchawanen_US
dc.contributor.authorPeraphan Pothacharoenen_US
dc.contributor.authorChaniporn Puanintaen_US
dc.contributor.authorRunchana Markmeeen_US
dc.contributor.authorWaleephan Tancharoenen_US
dc.contributor.authorTanongsak Laowanitwattanaen_US
dc.contributor.authorNaree Poovachiranonen_US
dc.contributor.authorChawapon Thaojamnongen_US
dc.date.accessioned2018-11-29T07:34:20Z-
dc.date.available2018-11-29T07:34:20Z-
dc.date.issued2018-01-01en_US
dc.identifier.issn16180372en_US
dc.identifier.issn00651281en_US
dc.identifier.other2-s2.0-85055911810en_US
dc.identifier.other10.1016/j.acthis.2018.10.009en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85055911810&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/62592-
dc.description.abstract© 2018 Elsevier GmbH Mesenchymal stem cells (MSCs), which possess remarkable capabilities, are found in amniotic fluid (AF). The findings of several studies have shown the potential benefits of these cells in applications of regenerative medicine. In clinical applications, an over-period of time is required in a preparation process that makes cell collection become more necessary. Herein, the aim of this study was to preserve and characterize the cell's properties after cell cryopreservation into an appropriate cryogenic medium. The results illustrated that the highest hAF-MSCs viability was found when the cells were conserved in a solution of 5% DMSO + 10% FBS in AF. However, no statistical differences were identified in a chromosomal aberration of the post-thawed cells when compared to the non-frozen cells. These cells could also maintain their MSC features through the ability to express cell prolific quality, illustrating the typical MSC markers and immune privilege properties of CD44, CD73, CD90 and HLA-ABC. Additionally, post-thawed cells were able to differentiate into chondrogenic lineage by exhibiting chondrogenic related genes (SOX9, AGC, COL2A1) and proteins (transcription factor SOX9 protein (SOX9), cartilage oligomeric matrix protein (COMP) and aggrecan core protein (AGC)), as well as to present sGAGs accumulation. Interestingly, the use of a transmission electron microscope (TEM) uncovered the enrichment of the rough endoplasmic reticulum (rER) that coincided with euchromatin and the prominent nucleolus in the chondrogenic-induced cells that are normally found in the cells of natural cartilage. All in all, this study manifested that AF can be a major consideration and applied for use as a co-mixture of cryogenic medium.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleAmniotic fluid: Source of valuable mesenchymal stem cells and alternatively used as cryopreserved solutionen_US
dc.typeJournalen_US
article.title.sourcetitleActa Histochemicaen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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