Accelerated Bone Reconstruction by the Yoda1 Bilayer Membrane via Promotion of Osteointegration and Angiogenesis

被引:11
|
作者
Yang, Jinghong [1 ]
Yuan, Kaiting [1 ]
Zhang, Tingting [1 ]
Zhou, Shiqi [1 ]
Li, Weichang [1 ]
Chen, Zetao [1 ]
Wang, Yan [1 ]
机构
[1] Sun Yat Sen Univ, Hosp Stomatol, Guanghua Sch Stomatol, Guangdong Prov Key Lab Stomatol, Guangzhou 510055, Guangdong, Peoples R China
关键词
bone regeneration; bilayer fibrous membranes; Yoda1; Piezo1; channel; angiogenesis; CHANNELS;
D O I
10.1002/adhm.202203105
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Guided bone regeneration membranes are widely used to prevent fibroblast penetration and facilitate bone defect repair by osteoblasts. However, the current clinically available collagen membranes lack bone induction and angiogenic capacities, exhibiting limited bone regeneration. The mechanically sensitive channel, Piezo1, which is activated by Yoda1, has been reported to play crucial roles in osteogenesis and angiogenesis. Nevertheless, the application of Yoda1 alone is unsustainable to maintain this activity. Therefore, this study fabricates a Yoda1-loading bilayer membrane using electrospinning technology. Its inner layer in contact with the bone defect is composed of vertically aligned fibers, which regulate the proliferation and differentiation of cells, release Yoda1, and promote bone regeneration. Its outer layer in contact with the soft tissue is dense with oriented fibers by UV cross-linking, mainly preventing fibroblast infiltration and inhibiting the immune response. Furthermore, the loaded Yoda1 affects osteogenesis and angiogenesis via the Piezo1/RhoA/Rho-associated coiled-coil-containing protein kinase 1/Yes1-associated transcriptional regulator signaling pathway. The results reveal that the Yoda1 bilayer membrane is efficient and versatile in accelerating bone regeneration, suggesting its potential as a novel therapeutic agent for various clinical issues.
引用
收藏
页数:17
相关论文
共 50 条
  • [21] Angelica dahurica promoted angiogenesis and accelerated wound healing in db/db mice via the HIF-1α/PDGF-β signaling pathway
    Guo, Jun
    Hu, Zhibo
    Yan, Fengjuan
    Lei, Sisi
    Li, Ting
    Li, Xiaoyu
    Xu, Chaofei
    Sun, Bei
    Pan, Congqing
    Chen, Liming
    FREE RADICAL BIOLOGY AND MEDICINE, 2020, 160 : 447 - 457
  • [22] AMIGO2, a novel membrane anchor of PDK1, controls cell survival and angiogenesis via Akt activation
    Park, Hyojin
    Lee, Sungwoon
    Shrestha, Pravesh
    Kim, Jihye
    Park, Jeong Ae
    Ko, Yeongrim
    Ban, Young Ho
    Park, Dae-Young
    Ha, Sang-Jun
    Koh, Gou Young
    Hong, Victor Sukbong
    Mochizuki, Naoki
    Kim, Young-Myeong
    Lee, Weontae
    Kwon, Young-Guen
    JOURNAL OF CELL BIOLOGY, 2015, 211 (03): : 619 - 637
  • [23] Crude Fucoidan Extracts Impair Angiogenesis in Models Relevant for Bone Regeneration and Osteosarcoma via Reduction of VEGF and SDF-1
    Wang, Fanlu
    Schmidt, Harald
    Pavleska, Dijana
    Wermann, Thees
    Seekamp, Andreas
    Fuchs, Sabine
    MARINE DRUGS, 2017, 15 (06):
  • [24] Nanog/NFATc1/Osterix signaling pathway-mediated promotion of bone formation at the tendon–bone interface after ACL reconstruction with De-BMSCs transplantation
    Kai Tie
    Jinghang Cai
    Jun Qin
    Hao Xiao
    Yangfan Shangguan
    Hui Wang
    Liaobin Chen
    Stem Cell Research & Therapy, 12
  • [25] Nanog/NFATc1/Osterix signaling pathway-mediated promotion of bone formation at the tendon-bone interface after ACL reconstruction with De-BMSCs transplantation
    Tie, Kai
    Cai, Jinghang
    Qin, Jun
    Xiao, Hao
    Shangguan, Yangfan
    Wang, Hui
    Chen, Liaobin
    STEM CELL RESEARCH & THERAPY, 2021, 12 (01)
  • [26] Protective effect of salidroside against bone loss via hypoxia-inducible factor-1α pathway-induced angiogenesis
    Li, Ling
    Qu, Ye
    Jin, Xin
    Guo, Xiao Qin
    Wang, Yue
    Qi, Lin
    Yang, Jing
    Zhang, Peng
    Li, Ling Zhi
    SCIENTIFIC REPORTS, 2016, 6
  • [27] Protective effect of salidroside against bone loss via hypoxia-inducible factor-1α pathway-induced angiogenesis
    Ling Li
    Ye Qu
    Xin Jin
    Xiao Qin Guo
    Yue Wang
    Lin Qi
    Jing Yang
    Peng Zhang
    Ling Zhi Li
    Scientific Reports, 6
  • [28] Bone morphogenetic protein 2 induces pulmonary angiogenesis via Wnt-β-catenin and Wnt-RhoA-Rac1 pathways
    Perez, Vinicio A. de Jesus
    Alastalo, Tero-Pekka
    Wu, Jenny C.
    Axelrod, Jeffrey D.
    Cooke, John P.
    Amieva, Manuel
    Rabinovitch, Marlene
    JOURNAL OF CELL BIOLOGY, 2009, 184 (01): : 83 - 99
  • [29] The Promotion of Bone Regeneration by the Chitosan-p24/hydroxyapatite Scaffold Via Modulation on Tgfβ-1/bmp/smad Signaling Pathway
    Yu, B.
    Chen, Y.
    Liu, R.
    Gong, Y.
    Spector, M.
    TISSUE ENGINEERING PART A, 2015, 21 : S179 - S179
  • [30] Bone Morphogenetic Protein Modulator BMPER Induces Angiogenesis via Inhibition of Thrombospondin-1 and Activation of the Fibroblast Growth Factor Signaling Pathway
    Esser, Jennifer S.
    Rahner, Susanne
    Deckler, Meike
    Bode, Christoph
    Moser, Martin
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2014, 34