Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.tice.2007.12.003
DC FieldValue
dc.titleAn autologous cell lysate extract from human embryonic stem cell (hESC) derived osteoblasts can enhance osteogenesis of hESC
dc.contributor.authorHeng, B.C.
dc.contributor.authorToh, W.S.
dc.contributor.authorPereira, B.P.
dc.contributor.authorTan, B.L.
dc.contributor.authorFu, X.
dc.contributor.authorLiu, H.
dc.contributor.authorLu, K.
dc.contributor.authorYeo, J.F.
dc.contributor.authorCao, T.
dc.date.accessioned2014-11-25T09:43:50Z
dc.date.available2014-11-25T09:43:50Z
dc.date.issued2008-06
dc.identifier.citationHeng, B.C., Toh, W.S., Pereira, B.P., Tan, B.L., Fu, X., Liu, H., Lu, K., Yeo, J.F., Cao, T. (2008-06). An autologous cell lysate extract from human embryonic stem cell (hESC) derived osteoblasts can enhance osteogenesis of hESC. Tissue and Cell 40 (3) : 219-228. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tice.2007.12.003
dc.identifier.issn00408166
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/108257
dc.description.abstractIt was recently demonstrated that osteogenesis of hESC was more efficient without the initial embryoid body formation step. This study sought to further improve this direct differentiation culture system, by developing an autologous osteogenic-inducing culture supplement extracted from hESC-derived osteogenic cells themselves. A whole cell lysate was prepared from hESC-derived osteogenic cells, simply by exposure to deionized water followed by free-thawing and subsequent filtration. The product was used to coat the surface of cell culture dishes together with gelatin, prior to culture of hESC under osteogenic-inducing conditions. The results showed that the autologous cell lysate extract promoted the aggregation and clustering of cells to form nodule-like structures. Immunohistochemical staining on day 9 demonstrated that these cellular aggregates strongly expressed STRO-1, while on day 14 the nodule-like structures stained positively for both osteocalcin and osteonectin (SPARC). By contrast, the negative control (gelatin coating alone) showed much less prominent cellular aggregation and clustering, and was stained much less intensely for these markers. Additionally, Von Kossa staining on day 14 was also more intense in the presence of the autologous cell lysate extract. Hence, this product can be used to further enhance the osteogenesis of hESC. This would save costs from the use of highly-expensive cytokines, growth factors and matrix components, as well as avoid pathogenic transmission from animal and human products. © 2007 Elsevier Ltd. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.tice.2007.12.003
dc.sourceScopus
dc.subjectAutologous
dc.subjectBone
dc.subjectEmbryonic stem cells
dc.subjectHuman
dc.subjectLysate
dc.subjectOsteogenesis
dc.typeArticle
dc.contributor.departmentORTHOPAEDIC SURGERY
dc.description.doi10.1016/j.tice.2007.12.003
dc.description.sourcetitleTissue and Cell
dc.description.volume40
dc.description.issue3
dc.description.page219-228
dc.description.codenTICEB
dc.identifier.isiut000256179400007
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.