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Mechanisms of ECM Scaffold Remodeling

Mechanisms of ECM Scaffold Remodeling
ECM支架改造机制
批准号:
7098054
负责人:
Stephen F. Badylak
金额:
$31.28万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-09-27 至 2007-07-31

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中文摘要
翻译
描述(由申请人提供): 这项修订提案的长期目标是开发组织工程策略,以促进用于组织和器官重建的支架的建设性重塑和血管化。目前的四年方案将以猪膀胱来源的异种细胞外基质(UB-ECM)作为测试支架材料,以两种动物模型作为临床前体内实验系统。关于支架重建机制的三个重要问题将被研究:1)参与重建过程的细胞的来源,2)支架降解与血管形成和组织重建的时空联系,以及3)在体外支架内种植和培养细胞以促进随后的体内血管形成和重建的概念。有四个具体的目标,每个目标都是通过控制的、精心设计的研究来解决的。第一个具体目标将检验宿主骨髓来源细胞作为支架重塑的多潜能细胞来源的概念。这一目标还将检验蛋白质交联对填充这些支架的细胞来源的影响。第二个具体目标将决定ECM支架的降解率、降解产物的命运以及支架降解与重建过程的关联。第三个和第四个特定目标将研究在体内植入之前,在ECM支架内分别培养血管壁前体细胞或骨髓来源的内皮前体细胞对支架重塑的影响。所有研究都基于广泛的初步数据和明确的假设。这些研究旨在了解支架重塑的机制,并将所学的原理应用于更广泛的组织工程应用。这项工作将由一个经验丰富的跨学科科学家小组进行,并提出了完成这项工作的时间表。
英文摘要
DESCRIPTION (provided by applicant): The long-term objective of this revised proposal is the development of tissue engineering strategies that will promote the constructive remodeling and vascularization of scaffolds used for tissue and organ reconstruction. The present four-year proposal would utilize xenogeneic extracellular matrix (ECM) derived from porcine urinary bladder (UB-ECM) as the test scaffold material and two animal models of esophageal reconstruction as the preclinical in vivo test system. Three important issues concerning the mechanisms of scaffold remodeling will be studied: 1) the source of cells that contribute to the remodeling process, 2) the temporal and spatial association of scaffold degradation with vascularization and tissue reconstruction, and 3) the concept of seeding and culturing cells within scaffolds in vitro to promote subsequent in vivo vascularization and remodeling. There are four Specific Aims, each of which is addressed by a controlled, carefully designed study. The first Specific Aim will examine the concept of host bone marrow-derived cells as a source of multi-potential cells for scaffold remodeling. This Aim will also examine the effect of protein cross-linking upon the source of cells that populate these scaffolds. The second Specific Aim will determine the rate of ECM scaffold degradation, the fate of degradation products, and the association of scaffold degradation with the remodeling process. The third and fourth Specific Aims will investigate the effect upon scaffold remodeling of culturing vascular mural precursor cells or marrow-derived endothelial precursor cells, respectively, within the ECM scaffold prior to in vivo implantation. All studies are based upon extensive preliminary data and upon clearly stated hypotheses. The studies are directed toward understanding the mechanisms of scaffold remodeling and applying the learned principles to broader tissue engineering applications. The work will be conducted by an experienced interdisciplinary team of scientists and a timeline is presented for completion of the work.
期刊论文(3)
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会议论文
DOI: 10.1016/j.biomaterials.2008.08.022
发表时间: 2008-12
期刊: Biomaterials
影响因子: 14
作者: [Gilbert TW, Wognum S, Joyce EM, Freytes DO, Sacks MS, Badylak SF]
通讯作者: Badylak SF
DOI: 10.2106/jbjs.e.00742
发表时间: 2007-03
期刊: The Journal of bone and joint surgery. American volume
影响因子: --
作者: [T. Gilbert;A. M. Stewart-Akers;A. Simmons-Byrd;S. Badylak]
通讯作者: T. Gilbert;A. M. Stewart-Akers;A. Simmons-Byrd;S. Badylak
Advanced Manufacturing of Regenerative Extracellular Matrix Scaffolds
  • 批准号:
    10001351
  • 项目类别:
  • 资助金额:
    $59.99万
  • 财政年份:
    2018
  • 负责人:
    Stephen F. Badylak
  • 依托单位:
Mechanisms of functional skeletal muscle repair: critical role of matrix associated IL-33
Advanced Manufacturing of Regenerative Extracellular Matrix Scaffolds
  • 批准号:
    9789233
  • 项目类别:
  • 资助金额:
    $59.97万
  • 财政年份:
    2018
  • 负责人:
    Stephen F. Badylak
  • 依托单位:
Bioengineering Tracheas Through Targeting Activated CD47
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