<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ramovs V</submitter><funding>Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW)</funding><pagination>1279-1288</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9213820</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(6)</volume><pubmed_abstract>Human induced pluripotent stem cell (hiPSC)-derived hair-bearing skin organoids offer exciting new possibilities for modeling diseases like epidermolysis bullosa (EB). These inherited diseases affect 1 in 30,000 people worldwide and result from perturbed expression and/or structure of components of the epidermal-dermal junction (EDJ). To establish whether hiPSC-derived skin organoids might be able to capture salient features of EB, it is thus important to characterize their EDJ. Here, we report successful generation of hair-bearing skin organoids from two hiPSC lines that exhibited fully stratified interfollicular epidermis. Using immunofluorescence and electron microscopy, we showed that basal keratinocytes in organoids adhere to laminin-332 and type IV collagen-rich basement membrane via</pubmed_abstract><journal>Stem cell reports</journal><pubmed_title>Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids.</pubmed_title><pmcid>PMC9213820</pmcid><funding_grant_id>reNEW LUMC</funding_grant_id><pubmed_authors>Janssen H</pubmed_authors><pubmed_authors>Raymond K</pubmed_authors><pubmed_authors>Freund C</pubmed_authors><pubmed_authors>Ramovs V</pubmed_authors><pubmed_authors>Rachidi W</pubmed_authors><pubmed_authors>Chuva de Sousa Lopes SM</pubmed_authors><pubmed_authors>Gidrol X</pubmed_authors><pubmed_authors>Mummery CL</pubmed_authors><pubmed_authors>Fuentes I</pubmed_authors><pubmed_authors>Pitaval A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids.</name><description>Human induced pluripotent stem cell (hiPSC)-derived hair-bearing skin organoids offer exciting new possibilities for modeling diseases like epidermolysis bullosa (EB). These inherited diseases affect 1 in 30,000 people worldwide and result from perturbed expression and/or structure of components of the epidermal-dermal junction (EDJ). To establish whether hiPSC-derived skin organoids might be able to capture salient features of EB, it is thus important to characterize their EDJ. Here, we report successful generation of hair-bearing skin organoids from two hiPSC lines that exhibited fully stratified interfollicular epidermis. Using immunofluorescence and electron microscopy, we showed that basal keratinocytes in organoids adhere to laminin-332 and type IV collagen-rich basement membrane via</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2026-05-27T20:29:00.834Z</modification><creation>2025-02-19T02:43:46.766Z</creation></dates><accession>S-EPMC9213820</accession><cross_references><pubmed>35561682</pubmed><doi>10.1016/j.stemcr.2022.04.008</doi></cross_references></HashMap>