Please use this identifier to cite or link to this item:
https://doi.org/10.1111/jcmm.13589
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dc.title | Postnatal periodontal ligament as a novel adult stem cell source for regenerative corneal cell therapy | |
dc.contributor.author | Yam, G.H.-F | |
dc.contributor.author | Teo, E.P.-W | |
dc.contributor.author | Setiawan, M | |
dc.contributor.author | Lovatt, M.J | |
dc.contributor.author | Yusoff, N.Z.B.M | |
dc.contributor.author | Fuest, M | |
dc.contributor.author | Goh, B.-T | |
dc.contributor.author | Mehta, J.S | |
dc.date.accessioned | 2020-09-09T10:06:20Z | |
dc.date.available | 2020-09-09T10:06:20Z | |
dc.date.issued | 2018 | |
dc.identifier.citation | Yam, G.H.-F, Teo, E.P.-W, Setiawan, M, Lovatt, M.J, Yusoff, N.Z.B.M, Fuest, M, Goh, B.-T, Mehta, J.S (2018). Postnatal periodontal ligament as a novel adult stem cell source for regenerative corneal cell therapy. Journal of Cellular and Molecular Medicine 22 (6) : 3119-3132. ScholarBank@NUS Repository. https://doi.org/10.1111/jcmm.13589 | |
dc.identifier.issn | 1582-1838 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/175381 | |
dc.description.abstract | Corneal opacities are a leading cause of global blindness. They are conventionally treated by the transplantation of donor corneal tissue, which is, restricted by a worldwide donor material shortage and allograft rejection. Autologous adult stem cells with a potential to differentiate into corneal stromal keratocytes (CSKs) could offer a suitable choice of cells for regenerative cell therapy. Postnatal periodontal ligament (PDL) contains a population of adult stem cells, which has a similar embryological origin as CSK, that is cranial neural crest. We harvested PDL cells from young adult teeth extracted because of non-functional or orthodontic reason and differentiated them towards CSK phenotype using a two-step protocol with spheroid formation followed by growth factor and cytokine induction in a stromal environment (human amnion stroma and porcine corneal stroma). Our results showed that the PDL-differentiated CSK-like cells expressed CSK markers (CD34, ALDH3A1, keratocan, lumican, CHST6, B3GNT7 and Col8A2) and had minimal expression of genes related to fibrosis and other lineages (vasculogenesis, adipogenesis, myogenesis, epitheliogenesis, neurogenesis and hematogenesis). Introduction of PDL spheroids into the stroma of porcine corneas resulted in extensive migration of cells inside the host stroma after 14-day organ culture. Their quiescent nature and uniform cell distribution resembled to that of mature CSKs inside the native stroma. Our results demonstrated the potential translation of PDL cells for regenerative corneal cell therapy for corneal opacities. © 2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. | |
dc.source | Unpaywall 20200831 | |
dc.subject | 5' nucleotidase | |
dc.subject | activated leukocyte cell adhesion molecule | |
dc.subject | aldehyde dehydrogenase | |
dc.subject | aldehyde dehydrogenase isoenzyme 3 a1 | |
dc.subject | angiopoietin 1 | |
dc.subject | carbohydrate sulfotransferase 6 | |
dc.subject | CD14 antigen | |
dc.subject | CD34 antigen | |
dc.subject | collagen type 8 | |
dc.subject | cycline | |
dc.subject | endoglin | |
dc.subject | Hermes antigen | |
dc.subject | keratocan | |
dc.subject | lumican | |
dc.subject | n acetylglucosaminyltransferase | |
dc.subject | nestin | |
dc.subject | phalloidin | |
dc.subject | platelet endothelial cell adhesion molecule 1 | |
dc.subject | receptor type tyrosine protein phosphatase C | |
dc.subject | sulfurtransferase | |
dc.subject | Thy 1 membrane glycoprotein | |
dc.subject | transcription factor FKHR | |
dc.subject | transcription factor GATA 4 | |
dc.subject | transcription factor Sox10 | |
dc.subject | transcription factor Sox2 | |
dc.subject | unclassified drug | |
dc.subject | adolescent | |
dc.subject | adult | |
dc.subject | adult stem cell | |
dc.subject | Article | |
dc.subject | cell differentiation | |
dc.subject | cell migration | |
dc.subject | cell proliferation | |
dc.subject | cell regeneration | |
dc.subject | cellular distribution | |
dc.subject | confocal microscopy | |
dc.subject | controlled study | |
dc.subject | cornea opacity | |
dc.subject | cornea stroma cell | |
dc.subject | extracellular matrix | |
dc.subject | female | |
dc.subject | fibroblast | |
dc.subject | flow cytometry | |
dc.subject | gene expression | |
dc.subject | genetic association | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | human tissue | |
dc.subject | immunohistochemistry | |
dc.subject | male | |
dc.subject | neural crest cell | |
dc.subject | periodontal ligament | |
dc.subject | phenotype | |
dc.subject | postnatal growth | |
dc.subject | priority journal | |
dc.subject | real time polymerase chain reaction | |
dc.subject | regenerative medicine | |
dc.subject | RNA extraction | |
dc.subject | upregulation | |
dc.subject | adult stem cell | |
dc.subject | animal | |
dc.subject | cell lineage | |
dc.subject | cell motion | |
dc.subject | cornea | |
dc.subject | cornea cell | |
dc.subject | cornea disease | |
dc.subject | cytology | |
dc.subject | genetics | |
dc.subject | growth, development and aging | |
dc.subject | neural crest | |
dc.subject | pathology | |
dc.subject | periodontal ligament | |
dc.subject | pig | |
dc.subject | transplantation | |
dc.subject | Adult Stem Cells | |
dc.subject | Animals | |
dc.subject | Cell Differentiation | |
dc.subject | Cell Lineage | |
dc.subject | Cell Movement | |
dc.subject | Cornea | |
dc.subject | Corneal Diseases | |
dc.subject | Corneal Keratocytes | |
dc.subject | Humans | |
dc.subject | Neural Crest | |
dc.subject | Periodontal Ligament | |
dc.subject | Regenerative Medicine | |
dc.subject | Swine | |
dc.type | Article | |
dc.contributor.department | DUKE-NUS MEDICAL SCHOOL | |
dc.description.doi | 10.1111/jcmm.13589 | |
dc.description.sourcetitle | Journal of Cellular and Molecular Medicine | |
dc.description.volume | 22 | |
dc.description.issue | 6 | |
dc.description.page | 3119-3132 | |
dc.published.state | Published | |
Appears in Collections: | Staff Publications Elements |
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