{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,15]],"date-time":"2026-10-15T15:42:20Z","timestamp":1792078940896,"version":"4.4.0"},"reference-count":50,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"7","content-domain":{"domain":["www.ahajournals.org"],"crossmark-restriction":true},"short-container-title":["Circulation"],"published-print":{"date-parts":[[2021,8,17]]},"abstract":"<jats:sec>\n                    <jats:title>Background:<\/jats:title>\n                    <jats:p>\n                      Pulmonary hypertension (PH) is a common complication in patients with alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV), a severe congenital disorder associated with mutations in the\n                      <jats:italic>FOXF1<\/jats:italic>\n                      gene. Although the loss of alveolar microvasculature causes PH in patients with ACDMPV, it is unknown whether increasing neonatal lung angiogenesis could prevent PH and right ventricular (RV) hypertrophy.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods:<\/jats:title>\n                    <jats:p>\n                      We used echocardiography, RV catheterization, immunostaining, and biochemical methods to examine lung and heart remodeling and RV output in\n                      <jats:italic>Foxf1<\/jats:italic>\n                      <jats:sup>\n                        <jats:italic>WT\/S52F<\/jats:italic>\n                      <\/jats:sup>\n                      mice carrying the\n                      <jats:italic>S52F Foxf1<\/jats:italic>\n                      mutation (identified in patients with ACDMPV). The ability of\n                      <jats:italic>Foxf1<\/jats:italic>\n                      <jats:sup>\n                        <jats:italic>WT\/S52F<\/jats:italic>\n                      <\/jats:sup>\n                      mutant embryonic stem cells to differentiate into respiratory cell lineages in vivo was examined using blastocyst complementation. Intravascular delivery of nanoparticles with a nonintegrating\n                      <jats:italic>Stat3<\/jats:italic>\n                      expression vector was used to improve neonatal pulmonary angiogenesis in\n                      <jats:italic>Foxf1<\/jats:italic>\n                      <jats:sup>\n                        <jats:italic>WT\/S52F<\/jats:italic>\n                      <\/jats:sup>\n                      mice and determine its effects on PH and RV hypertrophy.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results:<\/jats:title>\n                    <jats:p>\n                      <jats:italic>Foxf1<\/jats:italic>\n                      <jats:sup>\n                        <jats:italic>WT\/S52F<\/jats:italic>\n                      <\/jats:sup>\n                      mice developed PH and RV hypertrophy after birth. The severity of PH in\n                      <jats:italic>Foxf1<\/jats:italic>\n                      <jats:sup>\n                        <jats:italic>WT\/S52F<\/jats:italic>\n                      <\/jats:sup>\n                      mice directly correlated with mortality, low body weight, pulmonary artery muscularization, and increased collagen deposition in the lung tissue. Increased fibrotic remodeling was found in human ACDMPV lungs. Mouse embryonic stem cells carrying the\n                      <jats:italic>S52F Foxf1<\/jats:italic>\n                      mutation were used to produce chimeras through blastocyst complementation and to demonstrate that\n                      <jats:italic>Foxf1<\/jats:italic>\n                      <jats:sup>\n                        <jats:italic>WT\/S52F<\/jats:italic>\n                      <\/jats:sup>\n                      embryonic stem cells have a propensity to differentiate into pulmonary myofibroblasts. Intravascular delivery of nanoparticles carrying\n                      <jats:italic>Stat3<\/jats:italic>\n                      cDNA protected\n                      <jats:italic>Foxf1<\/jats:italic>\n                      <jats:sup>\n                        <jats:italic>WT\/S52F<\/jats:italic>\n                      <\/jats:sup>\n                      mice from RV hypertrophy and PH, improved survival, and decreased fibrotic lung remodeling.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions:<\/jats:title>\n                    <jats:p>Nanoparticle therapies increasing neonatal pulmonary angiogenesis may be considered to prevent PH in ACDMPV.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1161\/circulationaha.121.053980","type":"journal-article","created":{"date-parts":[[2021,6,11]],"date-time":"2021-06-11T05:02:56Z","timestamp":1623387776000},"page":"539-555","update-policy":"https:\/\/doi.org\/10.1161\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":62,"title":["Nanoparticle Delivery of STAT3 Alleviates Pulmonary Hypertension in a Mouse Model of Alveolar Capillary Dysplasia"],"prefix":"10.1161","volume":"144","author":[{"given":"Fei","family":"Sun","sequence":"first","affiliation":[{"name":"Center for Lung Regenerative Medicine, Perinatal Institute (F.S., G.W., A.P., K.X., J.G.-A., Y.Z., G.T.K., Z.D., A.W.D., V.V.K.), Cincinnati Children\u2019s Hospital Medical Center, OH."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Guolun","family":"Wang","sequence":"additional","affiliation":[{"name":"Center for Lung Regenerative Medicine, Perinatal Institute (F.S., G.W., A.P., K.X., J.G.-A., Y.Z., G.T.K., Z.D., A.W.D., 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