<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(1)</volume><submitter>Morgner B</submitter><funding>Universitätsklinikum Jena</funding><pubmed_abstract>Skin homeostasis is a complex regulated process relying on the crosstalk of keratinocytes, fibroblasts and immune cells. Imbalances of T-cell subsets and the cytokine environment can lead to inflammatory skin diseases such as psoriasis (Ps) and atopic dermatitis (AD). Modern tissue engineering provides several in vitro models mimicking Ps and AD phenotypes. However, these models are either limited in their pathological features, life span, sample availability, reproducibility, controlled handling or simplicity. Some models further lack intensive characterization as they solely focus on differentiation and proliferation aspects. This study introduces a self-assembly model in which the pathological T-cell-signalling of Ps and AD was simulated by subcutaneous Th1 and Th2 cytokine stimulation.</pubmed_abstract><journal>Scientific reports</journal><pagination>1807</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9889787</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Induction of psoriasis- and atopic dermatitis-like phenotypes in 3D skin equivalents with a fibroblast-derived matrix.</pubmed_title><pmcid>PMC9889787</pmcid><pubmed_authors>Tittelbach J</pubmed_authors><pubmed_authors>Wiegand C</pubmed_authors><pubmed_authors>Morgner B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Induction of psoriasis- and atopic dermatitis-like phenotypes in 3D skin equivalents with a fibroblast-derived matrix.</name><description>Skin homeostasis is a complex regulated process relying on the crosstalk of keratinocytes, fibroblasts and immune cells. Imbalances of T-cell subsets and the cytokine environment can lead to inflammatory skin diseases such as psoriasis (Ps) and atopic dermatitis (AD). Modern tissue engineering provides several in vitro models mimicking Ps and AD phenotypes. However, these models are either limited in their pathological features, life span, sample availability, reproducibility, controlled handling or simplicity. Some models further lack intensive characterization as they solely focus on differentiation and proliferation aspects. This study introduces a self-assembly model in which the pathological T-cell-signalling of Ps and AD was simulated by subcutaneous Th1 and Th2 cytokine stimulation.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-22T04:01:27.378Z</modification><creation>2025-04-05T20:51:18.301Z</creation></dates><accession>S-EPMC9889787</accession><cross_references><pubmed>36720910</pubmed><doi>10.1038/s41598-023-28822-7</doi></cross_references></HashMap>