Interaction between host cells and multicomponent material matrix

宿主细胞与多组分材料基质之间的相互作用

• 批准号: 7390248
• 负责人: WEIYUAN J KAO
• 金额: $ 24.55万
• 依托单位: UNIVERSITY OF WISCONSIN-MADISON
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-06-01 至 2010-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7390248
• 关键词: Affect; Architecture; Biochemical; Biocompatible Materials; Biological; Biological Process; Biological Sciences; Blood; Cell Culture System; Cell model; Cell physiology; Cells; Complement; Cues; Dermal; Development; Engineering; Event; Extracellular Matrix Proteins; Fibroblasts; Fibronectins; Fibrosis; Gelatin; Growth Factor; Healed; Human; Immune response; In Situ; Inflammation; Knowledge; Life; Mechanics; Mediating; Modeling; Normal tissue morphology; Oligopeptides; Peptides; Property; Reaction; Role; Signal Transduction; Staging; Structure-Activity Relationship; System; Technology; Time Study; Tissue Engineering; Tissues; biomaterial compatibility; cell behavior; cell type; clinical application; clinically relevant; healing; in vivo; keratinocyte; keratinocyte growth factor; macrophage; response

DESCRIPTION (provided by applicant): Biological processes (i.e., healing) operate at a multi-component hierarchy. To strengthen the fundamental engineering knowledge of cellular processes for material biocompatibility and tissue engineering, the elucidation of structure-function relationships and control mechanisms of host cells is critical. Our objective is to establish a clinically relevant multifunctional construct that provides several developmental signals to enhance the desirable response of host cells in the reestablishment of normal tissue architecture. Furthermore, this construct provides a microenvironment platform for us to study the mechanisms of soluble and immobilized bioactive factors on affecting cell function. The role of material physicochemical properties on this mediated cell behavior will be ascertained in tandem with the delivery of bioactive factors. We will employ model cell types for selected critical stages of host response to biomaterials (i.e., macrophages for inflammation, fibroblasts for granulation and fibrosis, and keratinocytes for end-stage healing by normal parenchymal cells) and model soluble and immobilized factors (i.e:, growth factors and extracellular matrix protein-derived peptides) as a platform in the study of time-dependent, material- modulated biological response. Our specific aims are: (1) To develop an in situ photopolymerizable interpenetrating network (IPN) system that consists of modified gelatin and polyethyleneglycol derivatives and contains soluble (i.e., keratinocyte growth factors) and immobilized (i.e., fibronectin derived oligopeptides) biofunctional factors. (2) To establish a mechanistic understanding of the independent and additive effect of aforementioned soluble and immobilized factors on the activation of model cell types (i.e., human blood-derived macrophages, dermal fibroblasts, and keratinocytes) using monoculture and binary cell culture systems. (3) To ascertain IPN efficacy in vivo in modulating the host reaction and healing.

描述(由申请人提供)：生物过程(即愈合)在多组分层次上运行。为了加强材料生物相容性和组织工程的细胞过程的基础工程知识，阐明宿主细胞的结构-功能关系和控制机制是至关重要的。我们的目标是建立一个与临床相关的多功能结构，提供几种发育信号，以增强宿主细胞在重建正常组织结构中的理想反应。此外，该构建为我们研究可溶性和固定化生物活性因子影响细胞功能的机制提供了一个微环境平台。材料的物理化学性质对这种介导的细胞行为的作用将随着生物活性因子的传递而被确定。我们将选择宿主对生物材料反应的关键阶段的模型细胞类型(即炎症的巨噬细胞，肉芽和纤维化的成纤维细胞，以及正常实质细胞的终末期愈合的角质形成细胞)和可溶的和固定化的因子(即生长因子和细胞外基质蛋白衍生的多肽)作为研究依赖时间的、材料调节的生物反应的平台。我们的具体目标是：(1)开发一种原位光聚合互穿网络(IPN)系统，该系统由修饰的明胶和聚乙二醇衍生物组成，包含可溶性(即角质形成细胞生长因子)和固定化(即纤维连接蛋白衍生的寡肽)生物功能因子。(2)利用单培养和双细胞培养系统，对上述可溶性和固定化因子对模型细胞(如人血源性巨噬细胞、真皮成纤维细胞和角质形成细胞)激活的独立和相加作用建立一个机制的理解。(3)确定IPN在体内对宿主反应和愈合的调节作用。