2010
DOI: 10.1167/iovs.09-4029
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Corneal Reconstruction with Tissue-Engineered Cell Sheets Composed of Human Immature Dental Pulp Stem Cells

Abstract: Overall, these data showed that transplantation of a tissue-engineered hIDPSC sheet was successful for the reconstruction of corneal epithelium in an animal model of LSCD.

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Cited by 232 publications
(156 citation statements)
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“…Pulp stem cells are thus enriched on their ability to form colonies (Gronthos et al, 2000), their expression of cell surface molecules such as STRO-1 (Gronthos et al, 2000), or CD34 (Laino et al, 2006) or on their capacity of exclusion of a DNA binding dye (Iohara et al, 2006). Not surprisingly, the resulting different cell populations display various differentiation potentials, upon appropriate in vitro induction (for review see Huang, 2009) and are able to participate in bone (d 'Aquino et al, 2009;Seo et al, 2008), neuronal (Arthur et al, 2008 and corneal tissue formation in vivo (Table 3; Gomes et al, 2010). In an implanted tooth slice model, heterogeneous populations of DPSCs, SCAPs or SHEDs have already shown their capacity to participate in the formation of a pulp-like tissue with dentin secretion and apposition (Huang et al, 2010;Sakai et al, 2010).…”
Section: Cell Sourcesmentioning
confidence: 99%
“…Pulp stem cells are thus enriched on their ability to form colonies (Gronthos et al, 2000), their expression of cell surface molecules such as STRO-1 (Gronthos et al, 2000), or CD34 (Laino et al, 2006) or on their capacity of exclusion of a DNA binding dye (Iohara et al, 2006). Not surprisingly, the resulting different cell populations display various differentiation potentials, upon appropriate in vitro induction (for review see Huang, 2009) and are able to participate in bone (d 'Aquino et al, 2009;Seo et al, 2008), neuronal (Arthur et al, 2008 and corneal tissue formation in vivo (Table 3; Gomes et al, 2010). In an implanted tooth slice model, heterogeneous populations of DPSCs, SCAPs or SHEDs have already shown their capacity to participate in the formation of a pulp-like tissue with dentin secretion and apposition (Huang et al, 2010;Sakai et al, 2010).…”
Section: Cell Sourcesmentioning
confidence: 99%
“…The longterm results of cultured autologous oral mucosal epithelial transplants remain to 115 9 Controversies in Corneal Epithelial Stem Cell Biology be determined. Other autologous cells being suggested as possibilities for treating limbal stem cell defi ciency include mesenchymal stem cells isolated from bone marrow or cells from the skin (Blazejewska et al 2009 ) or dental pulp (Gomes et al 2010 ) .…”
Section: How Can Bilateral Limbal Stem Cell Defi Ciency Be Treated?mentioning
confidence: 99%
“…Pulp stem cells are thus enriched on their ability to form colonies (Gronthos et al, 2000), their expression of cell surface molecules such as STRO-1 (Gronthos et al, 2000), or CD34 (Laino et al, 2006) or on their capacity of exclusion of a DNA binding dye (Iohara et al, 2006). Not surprisingly, the resulting different cell populations display various differentiation potentials, upon appropriate in vitro induction (for review see Huang, 2009) and are able to participate in bone (d 'Aquino et al, 2009;Seo et al, 2008), neuronal (Arthur et al, 2008) and corneal tissue formation in vivo (Table 3; Gomes et al, 2010). In an implanted tooth slice model, heterogeneous populations of DPSCs, SCAPs or SHEDs have already shown their capacity to participate in the formation of a pulp-like tissue with dentin secretion and apposition Sakai et al, 2010).…”
Section: Cell Sourcesmentioning
confidence: 99%