Localized COUP‐TFII pDNA Delivery Modulates Stem/Progenitor Cell Differentiation to Enhance Endothelialization and Inhibit Calcification of Decellularized Allografts
Abstract Decellularized allografts have emerged as promising candidates for vascular bypass grafting, owing to their inherent bioactivity and minimal immunogenicity. However, graft failure that results from suboptimal regeneration and pathological remodeling has hindered their clinical adoption. Rec...
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2025-02-01
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author | Mengmeng Xing Fei Wang Ruowen Chu He Wang Yuyao Sun Meng Qian Huan Jiang Adam C. Midgley Guohao Dai Qiang Zhao |
author_facet | Mengmeng Xing Fei Wang Ruowen Chu He Wang Yuyao Sun Meng Qian Huan Jiang Adam C. Midgley Guohao Dai Qiang Zhao |
author_sort | Mengmeng Xing |
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description | Abstract Decellularized allografts have emerged as promising candidates for vascular bypass grafting, owing to their inherent bioactivity and minimal immunogenicity. However, graft failure that results from suboptimal regeneration and pathological remodeling has hindered their clinical adoption. Recent advances in vascular biology highlight the pivotal role of COUP‐TFII in orchestrating endothelial identity, angiogenesis, safeguarding against atherosclerosis, and mitigating vascular calcification. Here, plasmid DNA (pDNA) encoding COUP‐TFII is incorporated into decellularized allografts to realize localized delivery. Comprehensive in vitro investigation complemented by a bone marrow transplantation model on genetic‐lineage‐tracing mouse revealed the underlying mechanisms of COUP‐TFII in regulating vascular regeneration and remodeling. COUP‐TFII augmented endothelialization and inhibited calcification in decellularized allografts by modulating the Ang1/Tie2/PI3K/AKT signaling pathway that dictates the fate of Sca‐1+ stem/progenitor cells. Heparin‐polyethyleneimine nanoparticles (HEPI) are prepared as COUP‐TFII pDNA nanocarriers (COUP‐TFII@HPEI) and used to modify decellularized allografts, achieving long‐term and stable overexpression of COUP‐TFII. Functionalized grafts are evaluated in rat abdominal artery replacement models, demonstrating enhanced neo‐artery regeneration without calcification. The study provides an effective strategy to enhance the applicability of decellularized allograft and illustrates their translational prospects for vascular bypass grafting. |
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language | English |
publishDate | 2025-02-01 |
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spelling | doaj-art-d51a6b5cc08c44dca20fe66d7347df4b2025-02-04T13:14:54ZengWileyAdvanced Science2198-38442025-02-01125n/an/a10.1002/advs.202409744Localized COUP‐TFII pDNA Delivery Modulates Stem/Progenitor Cell Differentiation to Enhance Endothelialization and Inhibit Calcification of Decellularized AllograftsMengmeng Xing0Fei Wang1Ruowen Chu2He Wang3Yuyao Sun4Meng Qian5Huan Jiang6Adam C. Midgley7Guohao Dai8Qiang Zhao9State key Laboratory of Medicinal Chemical Biology Frontiers Science Center for Cell Responses Key Laboratory of Bioactive Materials (Ministry of Education), College of Life Sciences Nankai University Tianjin 300071 ChinaState key Laboratory of Medicinal Chemical Biology Frontiers Science Center for Cell Responses Key Laboratory of Bioactive Materials (Ministry of Education), College of Life Sciences Nankai University Tianjin 300071 ChinaState key Laboratory of Medicinal Chemical Biology Frontiers Science Center for Cell Responses Key Laboratory of Bioactive Materials (Ministry of Education), College of Life Sciences Nankai University Tianjin 300071 ChinaState key Laboratory of Medicinal Chemical Biology Frontiers Science Center for Cell Responses Key Laboratory of Bioactive Materials (Ministry of Education), College of Life Sciences Nankai University Tianjin 300071 ChinaState key Laboratory of Medicinal Chemical Biology Frontiers Science Center for Cell Responses Key Laboratory of Bioactive Materials (Ministry of Education), College of Life Sciences Nankai University Tianjin 300071 ChinaState key Laboratory of Medicinal Chemical Biology Frontiers Science Center for Cell Responses Key Laboratory of Bioactive Materials (Ministry of Education), College of Life Sciences Nankai University Tianjin 300071 ChinaState key Laboratory of Medicinal Chemical Biology Frontiers Science Center for Cell Responses Key Laboratory of Bioactive Materials (Ministry of Education), College of Life Sciences Nankai University Tianjin 300071 ChinaState key Laboratory of Medicinal Chemical Biology Frontiers Science Center for Cell Responses Key Laboratory of Bioactive Materials (Ministry of Education), College of Life Sciences Nankai University Tianjin 300071 ChinaDepartment of Bioengineering Northeastern University BostonMA 02115 USAState key Laboratory of Medicinal Chemical Biology Frontiers Science Center for Cell Responses Key Laboratory of Bioactive Materials (Ministry of Education), College of Life Sciences Nankai University Tianjin 300071 ChinaAbstract Decellularized allografts have emerged as promising candidates for vascular bypass grafting, owing to their inherent bioactivity and minimal immunogenicity. However, graft failure that results from suboptimal regeneration and pathological remodeling has hindered their clinical adoption. Recent advances in vascular biology highlight the pivotal role of COUP‐TFII in orchestrating endothelial identity, angiogenesis, safeguarding against atherosclerosis, and mitigating vascular calcification. Here, plasmid DNA (pDNA) encoding COUP‐TFII is incorporated into decellularized allografts to realize localized delivery. Comprehensive in vitro investigation complemented by a bone marrow transplantation model on genetic‐lineage‐tracing mouse revealed the underlying mechanisms of COUP‐TFII in regulating vascular regeneration and remodeling. COUP‐TFII augmented endothelialization and inhibited calcification in decellularized allografts by modulating the Ang1/Tie2/PI3K/AKT signaling pathway that dictates the fate of Sca‐1+ stem/progenitor cells. Heparin‐polyethyleneimine nanoparticles (HEPI) are prepared as COUP‐TFII pDNA nanocarriers (COUP‐TFII@HPEI) and used to modify decellularized allografts, achieving long‐term and stable overexpression of COUP‐TFII. Functionalized grafts are evaluated in rat abdominal artery replacement models, demonstrating enhanced neo‐artery regeneration without calcification. The study provides an effective strategy to enhance the applicability of decellularized allograft and illustrates their translational prospects for vascular bypass grafting.https://doi.org/10.1002/advs.202409744calcificationCOUP‐TFIIdecellularized allograftsendothelial differentiationstem/progenitor cells (SPCs) |
spellingShingle | Mengmeng Xing Fei Wang Ruowen Chu He Wang Yuyao Sun Meng Qian Huan Jiang Adam C. Midgley Guohao Dai Qiang Zhao Localized COUP‐TFII pDNA Delivery Modulates Stem/Progenitor Cell Differentiation to Enhance Endothelialization and Inhibit Calcification of Decellularized Allografts Advanced Science calcification COUP‐TFII decellularized allografts endothelial differentiation stem/progenitor cells (SPCs) |
title | Localized COUP‐TFII pDNA Delivery Modulates Stem/Progenitor Cell Differentiation to Enhance Endothelialization and Inhibit Calcification of Decellularized Allografts |
title_full | Localized COUP‐TFII pDNA Delivery Modulates Stem/Progenitor Cell Differentiation to Enhance Endothelialization and Inhibit Calcification of Decellularized Allografts |
title_fullStr | Localized COUP‐TFII pDNA Delivery Modulates Stem/Progenitor Cell Differentiation to Enhance Endothelialization and Inhibit Calcification of Decellularized Allografts |
title_full_unstemmed | Localized COUP‐TFII pDNA Delivery Modulates Stem/Progenitor Cell Differentiation to Enhance Endothelialization and Inhibit Calcification of Decellularized Allografts |
title_short | Localized COUP‐TFII pDNA Delivery Modulates Stem/Progenitor Cell Differentiation to Enhance Endothelialization and Inhibit Calcification of Decellularized Allografts |
title_sort | localized coup tfii pdna delivery modulates stem progenitor cell differentiation to enhance endothelialization and inhibit calcification of decellularized allografts |
topic | calcification COUP‐TFII decellularized allografts endothelial differentiation stem/progenitor cells (SPCs) |
url | https://doi.org/10.1002/advs.202409744 |
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