{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T22:52:14Z","timestamp":1791931934474,"version":"4.3.4"},"reference-count":68,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2023,11,28]],"date-time":"2023-11-28T00:00:00Z","timestamp":1701129600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100017519","name":"Werner Otto Stiftung","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100017519","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Eur J Immunol"],"published-print":{"date-parts":[[2024,2]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>The initiation of tissue remodeling following damage is a critical step in preventing the development of immune\u2010mediated diseases. Several factors contribute to mucosal healing, leading to innovative therapeutic approaches for managing intestinal disorders. However, uncovering alternative targets and gaining mechanistic insights are imperative to enhance therapy efficacy and broaden its applicability across different intestinal diseases.<\/jats:p>\n                  <jats:p>\n                    Here we demonstrate that\n                    <jats:italic>Nmes1<\/jats:italic>\n                    , encoding for\n                    <jats:italic>Normal Mucosa of Esophagus\u2010Specific gene 1<\/jats:italic>\n                    , also known as\n                    <jats:italic>Aa467197<\/jats:italic>\n                    , is a novel regulator of mucosal healing.\n                    <jats:italic>Nmes1<\/jats:italic>\n                    influences the macrophage response to the tissue remodeling cytokine IL\u20104\n                    <jats:italic>in vitro<\/jats:italic>\n                    . In addition, using two murine models of intestinal damage, each characterized by a type 2\u2010dominated environment with contrasting functions, the ablation of\n                    <jats:italic>Nmes<\/jats:italic>\n                    1 results in decreased intestinal regeneration during the recovery phase of colitis, while enhancing parasitic egg clearance and reducing fibrosis during the advanced stages of\n                    <jats:italic>Schistosoma mansoni<\/jats:italic>\n                    infection. These outcomes are associated with alterations in CX3CR1\n                    <jats:sup>+<\/jats:sup>\n                    macrophages, cells known for their wound\u2010healing potential in the inflamed colon, hence promising candidates for cell therapies.\n                  <\/jats:p>\n                  <jats:p>\n                    All in all, our data indicate\n                    <jats:italic>Nmes1<\/jats:italic>\n                    as a novel contributor to mucosal healing, setting the basis for further investigation into its potential as a new target for the treatment of colon\u2010associated inflammation.\n                  <\/jats:p>","DOI":"10.1002\/eji.202350434","type":"journal-article","created":{"date-parts":[[2023,11,16]],"date-time":"2023-11-16T06:59:55Z","timestamp":1700117995000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["<i>Nmes1<\/i>\n                    is a novel regulator of mucosal response influencing intestinal healing potential"],"prefix":"10.1002","volume":"54","author":[{"given":"Madeleine","family":"Hamley","sequence":"first","affiliation":[{"name":"I. 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