Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/16959
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dc.contributor.authorMARTENS, Wendy-
dc.contributor.authorSANEN, Kathleen-
dc.contributor.authorGeorgiou, Melanie-
dc.contributor.authorSTRUYS, Tom-
dc.contributor.authorBRONCKAERS, Annelies-
dc.contributor.authorAMELOOT, Marcel-
dc.contributor.authorPhillips, James-
dc.contributor.authorLAMBRICHTS, Ivo-
dc.date.accessioned2014-07-14T09:32:21Z-
dc.date.available2014-07-14T09:32:21Z-
dc.date.issued2014-
dc.identifier.citationFASEB JOURNAL, 28 (4), p. 1634-1643-
dc.identifier.issn0892-6638-
dc.identifier.urihttp://hdl.handle.net/1942/16959-
dc.description.abstractIn the present study, we evaluated the differentiation potential of human dental pulp stem cells (hDPSCs) toward Schwann cells, together with their functional capacity with regard to myelination and support of neurite outgrowth in vitro. Successful Schwann cell differentiation was confirmed at the morphological and ultrastructural level by transmission electron microscopy. Furthermore, compared to undifferentiated hDPSCs, immunocytochemistry and ELISA tests revealed increased glial marker expression and neurotrophic factor secretion of differentiated hDPSCs (d-hDPSCs), which promoted survival and neurite outgrowth in 2-dimensional dorsal root ganglia cultures. In addition, neurites were myelinated by d-hDPSCs in a 3-dimensional collagen type I hydrogel neural tissue construct. This engineered construct contained aligned columns of d-hDPSCs that supported and guided neurite outgrowth. Taken together, these findings provide the first evidence that hDPSCs are able to undergo Schwann cell differentiation and support neural outgrowth in vitro, proposing them to be good candidates for cell-based therapies as treatment for peripheral nerve injury.-
dc.description.sponsorshipHasselt University (grant number 05G02BOF); Research Foundation Flanders [Fonds Wetenschappelijk Onderzoek (FWO)] (grant number K200713N); Interreg Euregio Meuse-Rhine IV-A consortium BioMIMedics; FWO (grant number GO29112FWO); Boehringer Ingelheim Fonds-
dc.language.isoen-
dc.rights© The Author(s).-
dc.subject.otherneural regeneration; nerve repair; glial cell; myelination; cellular hydrogel-
dc.titleHuman dental pulp stem cells can differentiate into Schwann cells and promote and guide neurite outgrowth in an aligned tissue-engineered collagen construct in vitro-
dc.typeJournal Contribution-
dc.identifier.epage1643-
dc.identifier.issue4-
dc.identifier.spage1634-
dc.identifier.volume28-
local.bibliographicCitation.jcatA1-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1096/fj.13-243980-
dc.identifier.isi000335344300012-
item.validationecoom 2015-
item.fulltextWith Fulltext-
item.accessRightsRestricted Access-
item.fullcitationMARTENS, Wendy; SANEN, Kathleen; Georgiou, Melanie; STRUYS, Tom; BRONCKAERS, Annelies; AMELOOT, Marcel; Phillips, James & LAMBRICHTS, Ivo (2014) Human dental pulp stem cells can differentiate into Schwann cells and promote and guide neurite outgrowth in an aligned tissue-engineered collagen construct in vitro. In: FASEB JOURNAL, 28 (4), p. 1634-1643.-
item.contributorMARTENS, Wendy-
item.contributorSANEN, Kathleen-
item.contributorGeorgiou, Melanie-
item.contributorSTRUYS, Tom-
item.contributorBRONCKAERS, Annelies-
item.contributorAMELOOT, Marcel-
item.contributorPhillips, James-
item.contributorLAMBRICHTS, Ivo-
crisitem.journal.issn0892-6638-
crisitem.journal.eissn1530-6860-
Appears in Collections:Research publications
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