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    Please use this identifier to cite or link to this item: http://ir.cnu.edu.tw/handle/310902800/32650


    標題: Sphingosine-1-phosphate in Endothelial Cell Recellularization Improves Patency and Endothelialization of Decellularized Vascular Grafts In Vivo
    作者: Hsia, Kai
    Lin, Chih-Hsun
    Lee, Hsin-Yu
    Chen, Wei-Min
    Yao, Chao-Ling
    Mark Chien-Chin Chen(陳建欽)
    Ma, Hsu
    Wang, Shyh-Jen
    Lu, Jen-Her
    貢獻者: Natl Taiwan Univ, Dept Life Sci
    Taipei Vet Gen Hosp, Dept Pediat
    Taipei Vet Gen Hosp, Div Plast Surg, Dept Surg
    Natl Yang Ming Univ, Sch Med, Dept Surg
    Yuan Ze Univ, Dept Chem Engn & Mat Sci, Grad Sch Biotechnol & Bioengn
    Chia Yi Christian Hosp, Dept Pathol, Ditmanson Med Fdn
    Chia Nan Univ Pharm & Sci, Dept Cosmet Sci
    Natl Def Med Ctr, Dept Surg Med & Pediat, Sch Med
    Taipei Vet Gen Hosp, Div Expt Surg, Dept Surg
    Natl Yang Ming Univ, Sch Med, Dept Pediat
    關鍵字: sphingosine-1-phosphate
    vascular graft
    endothelial cell
    thrombosis
    syndecan-1
    日期: 2019-04
    上傳時間: 2020-07-29 13:53:44 (UTC+8)
    出版者: MDPI
    摘要: Background: S1P has been shown to improve the endothelialization of decellularized vascular grafts in vitro. Here, we evaluated the potential of tissue-engineered vascular grafts (TEVGs) constructed by ECs and S1P on decellularized vascular scaffolds in a rat model. Methods: Rat aorta was decellularized mainly by 0.1% SDS and characterized by histology. Rat ECs, were seeded onto decellularized scaffolds, and the viability of the ECs was evaluated by biochemical assays. Then, we investigated the in vivo patency rate and endothelialization for five groups of decellularized vascular grafts (each n = 6) in a rat abdominal aorta model for 14 days. The five groups included (1) rat allogenic aorta (RAA); (2) decellularized RAA (DRAA); (3) DRAA with S1P (DRAA/S1P); (4) DRAA with EC recellularization (DRAA/EC); and (5) DRAA with S1P and EC recellularization (DRAA/EC/S1P). Results: In vitro, ECs were identified by the uptake of Dil-Ac-LDL. S1P enhanced the expression of syndecan-1 on ECs and supported the proliferation of ECs on decellularized vascular grafts. In vivo, RAA and DRAA/EC/S1P both had 100% patency without thrombus formation within 14 days. Better endothelialization, more wall structure maintenance and less inflammation were noted in the DRAA/EC/S1P group. In contrast, there was thrombus formation in the DRAA, DRAA/S1P and DRAA/EC groups. Conclusion: S1P could inhibit thrombus formation to improve the patency rate of EC-covered decellularized vascular grafts in vivo and may play an important role in the construction of TEVGs.
    關聯: International Journal of Molecular Sciences, v.20, n.7, 1641
    Appears in Collections:[化妝品應用與管理系(所)] 期刊論文

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