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Atherosclerotic three-layer nanomatrix vascular sheets for high-throughput therapeutic evaluation.
Chen, Jun; Zhang, Xixi; Cross, Robbie; Ahn, Yujin; Huskin, Gillian; Evans, Will; Hwang, Patrick Taejoon; Kim, Jeong-A; Brott, Brigitta C; Jo, Hanjoong; Yoon, Young-Sup; Jun, Ho-Wook.
Afiliação
  • Chen J; Department of Biomedical Engineering, The University of Alabama at Birmingham, Birmingham, AL, USA; Endomimetics, LLC., Birmingham, AL, USA.
  • Zhang X; Department of Biomedical Engineering, The University of Alabama at Birmingham, Birmingham, AL, USA.
  • Cross R; Department of Biomedical Engineering, The University of Alabama at Birmingham, Birmingham, AL, USA.
  • Ahn Y; Department of Biomedical Engineering, The University of Alabama at Birmingham, Birmingham, AL, USA.
  • Huskin G; Department of Biomedical Engineering, The University of Alabama at Birmingham, Birmingham, AL, USA.
  • Evans W; Augusta University/University of Georgia Medical Partnership, Athens, GA, USA.
  • Hwang PT; Endomimetics, LLC., Birmingham, AL, USA.
  • Kim JA; Department of Medicine, Division of Endocrinology and Metabolism, UAB Comprehensive Diabetes Center, Birmingham, AL, USA.
  • Brott BC; Endomimetics, LLC., Birmingham, AL, USA; Department of Medicine and Division of Cardiovascular Disease, The University of Alabama at Birmingham, AL, USA.
  • Jo H; Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA, USA.
  • Yoon YS; Division of Cardiology, School of Medicine, Emory University, Atlanta, GA, USA.
  • Jun HW; Department of Biomedical Engineering, The University of Alabama at Birmingham, Birmingham, AL, USA; Endomimetics, LLC., Birmingham, AL, USA. Electronic address: hwjun@uab.edu.
Biomaterials ; 305: 122450, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38169190
ABSTRACT
In vitro atherosclerosis models are essential to evaluate therapeutics before in vivo and clinical studies, but significant limitations remain, such as the lack of three-layer vascular architecture and limited atherosclerotic features. Moreover, no scalable 3D atherosclerosis model is available for making high-throughput assays for therapeutic evaluation. Herein, we report an in vitro 3D three-layer nanomatrix vascular sheet with critical atherosclerosis multi-features (VSA), including endothelial dysfunction, monocyte recruitment, macrophages, extracellular matrix remodeling, smooth muscle cell phenotype transition, inflammatory cytokine secretion, foam cells, and calcification initiation. Notably, we present the creation of high-throughput functional assays with VSAs and the use of these assays for evaluating therapeutics for atherosclerosis treatment. The therapeutics include conventional drugs (statin and sirolimus), candidates for treating atherosclerosis (curcumin and colchicine), and potential gene therapy (miR-146a-loaded liposomes). The high efficiency and flexibility of the scalable VSA functional assays should facilitate drug discovery and development for atherosclerosis.
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Texto completo: 1 Base de dados: MEDLINE Métodos Terapêuticos e Terapias MTCI: Plantas_medicinales Assunto principal: Aterosclerose / Placa Aterosclerótica Idioma: En Revista: Biomaterials Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Métodos Terapêuticos e Terapias MTCI: Plantas_medicinales Assunto principal: Aterosclerose / Placa Aterosclerótica Idioma: En Revista: Biomaterials Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos