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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Main Authors: Mengmeng Xing, Fei Wang, Ruowen Chu, He Wang, Yuyao Sun, Meng Qian, Huan Jiang, Adam C. Midgley, Guohao Dai, Qiang Zhao
Format: Article
Language:English
Published: Wiley 2025-02-01
Series:Advanced Science
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Online Access:https://doi.org/10.1002/advs.202409744
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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
collection DOAJ
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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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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