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A bilayer bioengineered patch with sequential dual-growth factor release to promote vascularization in bladder reconstruction.
Zhao, Jian; Zhang, Haoqian; Ling, Zhengyun; An, Ziyan; Xiao, Shuwei; Wang, Pengchao; Fu, Zhouyang; Shao, Jinpeng; Sun, Yanfeng; Fu, Weijun.
Affiliation
  • Zhao J; Medical School of PLA, Beijing 100853, China.
  • Zhang H; Department of Urology, The Third Medical Center, PLA General Hospital, Beijing 100039, China.
  • Ling Z; Department of Urology, 960th Hospital of PLA, Jinan 250031, China.
  • An Z; Inner Mongolia Medical University, Hohhot, Inner Mongolia 010050, China.
  • Xiao S; Department of Urology, The Third Medical Center, PLA General Hospital, Beijing 100039, China.
  • Wang P; School of Medicine, Nankai University, Tianjin 300071, China.
  • Fu Z; Medical School of PLA, Beijing 100853, China.
  • Shao J; Department of Urology, The Third Medical Center, PLA General Hospital, Beijing 100039, China.
  • Sun Y; Department of Urology, Air Force Medical Center, Beijing 100142, China.
  • Fu W; Department of Urology, The Third Medical Center, PLA General Hospital, Beijing 100039, China.
Regen Biomater ; 11: rbae083, 2024.
Article in En | MEDLINE | ID: mdl-39077683
ABSTRACT
Bladder tissue engineering holds promise for addressing bladder defects resulting from congenital or acquired bladder diseases. However, inadequate vascularization significantly impacts the survival and function of engineered tissues after transplantation. Herein, a novel bilayer silk fibroin (BSF) scaffold was fabricated with the capability of vascular endothelial growth factor (VEGF) and platelet derived growth factor-BB (PDGF-BB) sequential release. The outer layer of the scaffold was composed of compact SF film with waterproofness to mimic the serosa of the bladder. The inner layer was constructed of porous SF matrix incorporated with SF microspheres (MS) loaded with VEGF and PDGF-BB. We found that the 5% (w/v) MS-incorporated scaffold exhibited a rapid release of VEGF, whereas the 0.2% (w/v) MS-incorporated scaffold demonstrated a slow and sustained release of PDGF-BB. The BSF scaffold exhibited good biocompatibility and promoted endothelial cell migration, tube formation and enhanced endothelial differentiation of adipose derived stem cells (ADSCs) in vitro. The BSF patch was constructed by seeding ADSCs on the BSF scaffold. After in vivo transplantation, not only could the BSF patch facilitate the regeneration of urothelium and smooth muscle, but more importantly, stimulate the regeneration of blood vessels. This study demonstrated that the BSF patch exhibited excellent vascularization capability in bladder reconstruction and offered a viable functional bioengineered patch for future clinical studies.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Regen Biomater Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Regen Biomater Year: 2024 Document type: Article Affiliation country: China