{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"submitter":["An L"],"funding":["NIAMS NIH HHS"],"pubmed_abstract":["Vitiligo is an autoimmune skin disease caused by cutaneous melanocyte loss. Although phototherapy and T cell suppression therapy have been widely used to induce epidermal repigmentation, full pigmentation recovery is rarely achieved due to our poor understanding of the cellular and molecular mechanisms governing this process. Here, we identify unique melanocyte stem cell (McSC) epidermal migration rates between male and female mice, which is due to sexually dimorphic cutaneous inflammatory responses generated by ultra-violet B exposure. Using genetically engineered mouse models, and unbiased bulk and single-cell mRNA sequencing approaches, we determine that manipulating the inflammatory response through cyclooxygenase and its downstream prostaglandin product regulates McSC proliferation an"],"journal":["bioRxiv : the preprint server for biology"],"pagination":["2023.05.22.541644"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10245926"],"repository":["biostudies-literature"],"pubmed_title":["Sexual dimorphism in melanocyte stem cell behavior reveals combinational therapeutic strategies for cutaneous repigmentation."],"pmcid":["PMC10245926"],"funding_grant_id":["R01 AR075755"],"pubmed_authors":["Kim D","Nishimura N","Donahue L","Chi-Yong E","White AC","An L","Mejooli MA"],"additional_accession":[]},"is_claimable":false,"name":"Sexual dimorphism in melanocyte stem cell behavior reveals combinational therapeutic strategies for cutaneous repigmentation.","description":"Vitiligo is an autoimmune skin disease caused by cutaneous melanocyte loss. Although phototherapy and T cell suppression therapy have been widely used to induce epidermal repigmentation, full pigmentation recovery is rarely achieved due to our poor understanding of the cellular and molecular mechanisms governing this process. Here, we identify unique melanocyte stem cell (McSC) epidermal migration rates between male and female mice, which is due to sexually dimorphic cutaneous inflammatory responses generated by ultra-violet B exposure. Using genetically engineered mouse models, and unbiased bulk and single-cell mRNA sequencing approaches, we determine that manipulating the inflammatory response through cyclooxygenase and its downstream prostaglandin product regulates McSC proliferation an","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 May","modification":"2026-04-08T13:18:36.322Z","creation":"2025-02-19T03:19:26.502Z"},"accession":"S-EPMC10245926","cross_references":{"pubmed":["37293072"],"doi":["10.1101/2023.05.22.541644"]}}