Please use this identifier to cite or link to this item: https://doi.org/10.1111/jcmm.13589
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dc.titlePostnatal periodontal ligament as a novel adult stem cell source for regenerative corneal cell therapy
dc.contributor.authorYam, G.H.-F
dc.contributor.authorTeo, E.P.-W
dc.contributor.authorSetiawan, M
dc.contributor.authorLovatt, M.J
dc.contributor.authorYusoff, N.Z.B.M
dc.contributor.authorFuest, M
dc.contributor.authorGoh, B.-T
dc.contributor.authorMehta, J.S
dc.date.accessioned2020-09-09T10:06:20Z
dc.date.available2020-09-09T10:06:20Z
dc.date.issued2018
dc.identifier.citationYam, 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.issn1582-1838
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/175381
dc.description.abstractCorneal 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.sourceUnpaywall 20200831
dc.subject5' nucleotidase
dc.subjectactivated leukocyte cell adhesion molecule
dc.subjectaldehyde dehydrogenase
dc.subjectaldehyde dehydrogenase isoenzyme 3 a1
dc.subjectangiopoietin 1
dc.subjectcarbohydrate sulfotransferase 6
dc.subjectCD14 antigen
dc.subjectCD34 antigen
dc.subjectcollagen type 8
dc.subjectcycline
dc.subjectendoglin
dc.subjectHermes antigen
dc.subjectkeratocan
dc.subjectlumican
dc.subjectn acetylglucosaminyltransferase
dc.subjectnestin
dc.subjectphalloidin
dc.subjectplatelet endothelial cell adhesion molecule 1
dc.subjectreceptor type tyrosine protein phosphatase C
dc.subjectsulfurtransferase
dc.subjectThy 1 membrane glycoprotein
dc.subjecttranscription factor FKHR
dc.subjecttranscription factor GATA 4
dc.subjecttranscription factor Sox10
dc.subjecttranscription factor Sox2
dc.subjectunclassified drug
dc.subjectadolescent
dc.subjectadult
dc.subjectadult stem cell
dc.subjectArticle
dc.subjectcell differentiation
dc.subjectcell migration
dc.subjectcell proliferation
dc.subjectcell regeneration
dc.subjectcellular distribution
dc.subjectconfocal microscopy
dc.subjectcontrolled study
dc.subjectcornea opacity
dc.subjectcornea stroma cell
dc.subjectextracellular matrix
dc.subjectfemale
dc.subjectfibroblast
dc.subjectflow cytometry
dc.subjectgene expression
dc.subjectgenetic association
dc.subjecthuman
dc.subjecthuman cell
dc.subjecthuman tissue
dc.subjectimmunohistochemistry
dc.subjectmale
dc.subjectneural crest cell
dc.subjectperiodontal ligament
dc.subjectphenotype
dc.subjectpostnatal growth
dc.subjectpriority journal
dc.subjectreal time polymerase chain reaction
dc.subjectregenerative medicine
dc.subjectRNA extraction
dc.subjectupregulation
dc.subjectadult stem cell
dc.subjectanimal
dc.subjectcell lineage
dc.subjectcell motion
dc.subjectcornea
dc.subjectcornea cell
dc.subjectcornea disease
dc.subjectcytology
dc.subjectgenetics
dc.subjectgrowth, development and aging
dc.subjectneural crest
dc.subjectpathology
dc.subjectperiodontal ligament
dc.subjectpig
dc.subjecttransplantation
dc.subjectAdult Stem Cells
dc.subjectAnimals
dc.subjectCell Differentiation
dc.subjectCell Lineage
dc.subjectCell Movement
dc.subjectCornea
dc.subjectCorneal Diseases
dc.subjectCorneal Keratocytes
dc.subjectHumans
dc.subjectNeural Crest
dc.subjectPeriodontal Ligament
dc.subjectRegenerative Medicine
dc.subjectSwine
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1111/jcmm.13589
dc.description.sourcetitleJournal of Cellular and Molecular Medicine
dc.description.volume22
dc.description.issue6
dc.description.page3119-3132
dc.published.statePublished
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