{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,7,30]],"date-time":"2025-07-30T16:12:23Z","timestamp":1753891943884,"version":"3.41.2"},"reference-count":49,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2023,7,14]],"date-time":"2023-07-14T00:00:00Z","timestamp":1689292800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Pediatr."],"abstract":"<jats:sec><jats:title>Rationale<\/jats:title><jats:p>The role of circulating fetal monocytes in bronchopulmonary dysplasia is not known. We utilized a humanized mouse model that supports human progenitor cell engraftment (MISTRG) to test the hypothesis that prenatal monocyte programming alters early lung development and response to hyperoxia.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Cord blood-derived monocytes from 10 human infants were adoptively transferred into newborn MISTRG mice at p0 (1\u2009\u00d7\u200910<jats:sup>6<\/jats:sup> cells\/mouse, intrahepatic injection) followed by normoxia versus hyperoxia (85% oxygen\u2009\u00d7\u200914 days). Lungs were harvested at p14 for alveolar histology (alveolar count, perimeter and area) and vascular parameters (vWF staining for microvessel density, Fulton's index). Human CD45 staining was conducted to compare presence of hematopoietic cells. Murine lung parameters were compared among placebo and monocyte-injected groups. The individual profiles of the 10 patients were further considered, including gestational age (GA; <jats:italic>n<\/jats:italic>\u2009=\u20092 term, <jats:italic>n<\/jats:italic>\u2009=\u20093 moderate\/late preterm, and <jats:italic>n<\/jats:italic>\u2009=\u20095 very preterm infants) and preeclampsia (<jats:italic>n<\/jats:italic>\u2009=\u20094 patients). To explore the monocyte microenvironment of these patients, 30 cytokines\/chemokines were measured in corresponding human plasma by multiplex immunoassay.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Across the majority of patients and corresponding mice, MISTRG alveolarization was simplified and microvessel density was decreased following hyperoxia. Hyperoxia-induced changes were seen in both placebo (PBS) and monocyte-injected mice. Under normoxic conditions, alveolar development was altered modestly by monocytes as compared with placebo (<jats:italic>P<\/jats:italic>\u2009&amp;lt;\u20090.05). Monocyte injection was associated with increased microvessel density at P14 as compared with placebo (26.7\u2009\u00b1\u20090.73 vs. 18.8\u2009\u00b1\u20091.7 vessels per lung field; <jats:italic>P<\/jats:italic>\u2009&amp;lt;\u20090.001). Pooled analysis of patients revealed that injection of monocytes from births complicated by lower GA and preeclampsia was associated with changes in alveolarization and vascularization under normoxic conditions. These differences were modified by hyperoxia. CD45+ cell count was positively correlated with plasma monocyte chemoattractant protein-1 (<jats:italic>P<\/jats:italic>\u2009&amp;lt;\u20090.001) and macrophage inflammatory protein-1\u03b2 (<jats:italic>P<\/jats:italic>\u2009&amp;lt;\u20090.01). Immunohistochemical staining for human CD206 and mouse F4\/80 confirmed absence of macrophages in MISTRG lungs at P14.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Despite the inherent absence of macrophages in early stages of lung development, immunodeficient MISTRG mice revealed changes in alveolar and microvascular development induced by human monocytes. MISTRG mice exposed to neonatal hyperoxia may serve as a novel model to study isolated effects of human monocytes on alveolar and pulmonary vascular development.<\/jats:p><\/jats:sec>","DOI":"10.3389\/fped.2023.1146014","type":"journal-article","created":{"date-parts":[[2023,7,14]],"date-time":"2023-07-14T21:51:14Z","timestamp":1689371474000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":1,"title":["Development of a novel humanized mouse model to study bronchopulmonary dysplasia"],"prefix":"10.3389","volume":"11","author":[{"given":"Rob","family":"Birkett","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Janu","family":"Newar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Abhineet 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