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<dc:creator>Galindo, Sara</dc:creator>
<dc:creator>López Paniagua, Marina</dc:creator>
<dc:creator>De La Mata Sampedro, Ana</dc:creator>
<dc:creator>Herreras Cantalapiedra, José María</dc:creator>
<dc:creator>García Vázquez, Carmen</dc:creator>
<dc:creator>Marceñido, Beatriz</dc:creator>
<dc:creator>Rey, Esther</dc:creator>
<dc:creator>Higuera Barón, Celia</dc:creator>
<dc:creator>Calonge, Margarita</dc:creator>
<dc:creator>Nieto Miguel, Teresa</dc:creator>
<dc:date>2026</dc:date>
<dc:description>Producción Científica</dc:description>
<dc:description>Ocular limbal stem cell deficiency (LSCD) occurs because of corneal epithelial stem cell destruction or&#xd;
dysfunction at the limbal niche. LSCD can cause corneal blindness, and the current therapy based on limbal stem&#xd;
cell transplantation is continuously improving. The aim of this work was to compare the safety and efficacy of&#xd;
human mesenchymal stem cells (hMSCs) derived from bone marrow (hBM-MSCs) and adipose tissue (hAT-MSCs)&#xd;
when transplanted to a rabbit model of LSCD. Both hMSC types expressed the corneal and limbal epithelial cell&#xd;
markers CK3, CK12, ZO-1, and ABCG2 under standard culture conditions. A few hBM-MSCs expressed CK7 and E-&#xd;
cadherin, while hAT-MSCs expressed more CK7 but no E-cadherin. The hMSCs were seeded onto amniotic&#xd;
membranes and transplanted onto the ocular surface of a LSCD rabbit model. Both hMSC types were well&#xd;
tolerated without immunosuppression and were primarily located in the superior limbal stroma eight weeks post-&#xd;
transplantation. The hBM-MSC–treated group showed less superficial neovascularization, while the hAT-&#xd;
MSC–treated group showed less conjunctival invasion and fewer corneal stromal blood vessels. Compared to the&#xd;
untreated LSCD group, both hMSC-treated groups had less corneal opacity, less corneal and limbal stromal&#xd;
inflammation, and more corneal epithelial layers that partially recovered the corneal and limbal epithelial&#xd;
markers CK3, CK15, and p63. Overall, transplantation of hBM-MSCs and hAT-MSCs in a rabbit LSCD model&#xd;
reduced the development of corneal opacity, neovascularization, inflammation, and partially restored corneal&#xd;
and limbal tissue structure and epithelial cell phenotypes. Therefore, both types of hMSCs could become valid&#xd;
alternatives for LSCD treatment.</dc:description>
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<dc:identifier>https://uvadoc.uva.es/handle/10324/80765</dc:identifier>
<dc:language>eng</dc:language>
<dc:publisher>Elsevier</dc:publisher>
<dc:subject>3201.09 Oftalmología</dc:subject>
<dc:title>Bone marrow-versus adipose tissue-derived mesenchymal stem cells for corneal failure in an experimental model of limbal stem cell deficiency</dc:title>
<dc:type>info:eu-repo/semantics/article</dc:type>
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