Regulation of Epidermal Differentiation on Engineered Polymer Substrates

工程聚合物基质上表皮分化的调节

• 批准号: 7749014
• 负责人: John Thomas Connelly
• 金额: $ 3.48万
• 依托单位: CANCER RESEARCH UK CAMBRIDGE RES INST
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-12-01 至 2010-09-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7749014
• 关键词: 2-hydroxyethyl methacrylate; 4-Hydroxy-Tamoxifen; Adhesions; Adhesives; Area; Arginine; Aspartic Acid; Behavior; Biocompatible Materials; Biological Assay; Biomedical Engineering; Bromodeoxyuridine; CD34 gene; Caliber; Cell Density; Cell Line; Cell Lineage; Cell Proliferation; Cell physiology; Cells; Cellular Morphology; Cellular biology; Centrifugation; Complex; Cues; Cultured Cells; Development; Dose; Engineering; Environment; Epidermis; Ethylene Glycols; Exposure to; Extracellular Matrix; Fibronectins; Glycine; Goals; Hair follicle structure; Immunofluorescence Immunologic; In Vitro; Integrins; Island; Ker10 protein; Keratin; Ligands; Measures; Mediating; Morphology; Mouse Strains; Mus; Oligonucleotides; Pathology; Pathway interactions; Pattern; Play; Polymer Chemistry; Polymers; Positioning Attribute; Proteins; RGD (sequence); Regulation; Research; Research Institute; Research Proposals; Resistance; Role; Signal Pathway; Signal Transduction; Skin; Skin Cancer; Stem cells; Surface; System; Therapeutic Agents; Transgenes; Transgenic Mice; Transgenic Organisms; Wild Type Mouse; Work; base; beta catenin; c-myc Genes; cancer cell; density; ethylene glycol; improved; insight; involucrin; keratin 7; keratinocyte; keratinocyte differentiation; laminin-5; light microscopy; loricrin; migration; nile red; notch protein; novel; polymerization; promoter; receptor; research study; response; self-renewal; stem cell biology; stem cell differentiation; synthetic peptide; tool; tumor

DESCRIPTION (provided by applicant): Integrin-mediated adhesion plays a central role in numerous cellular processes including proliferation, migration, and differentiation. Within the epidermis of the skin, integrin receptors are known to influence stem cell differentiation; however, the mechanism by which cues from the ECM coordinate with other signaling pathways to determine cell fate remains unclear. The overall goal of this research proposal is to investigate the interaction between integrin-mediated adhesion and beta-catenin related signaling pathways in the regulation of epidermal differentiation. The proposed studies will employ engineered polymer substrates to control the type, density, and spatial organization of cell-adhesive ligands presented to the cells. The influences of these defined cell-matrix interactions on epidermal differentiation will be examined using keratinocytes isolated from wild type mice and transgenic mice with inducible beta-catenin, Notch, and c-Myc expression. The central hypothesis for this work is that integrin-mediated adhesion to the extracellular matrix regulates keratinocyte differentiation and that these responses are modulated by the strength of beta-catenin signaling and other related pathways. This research will be carried out in three specific aims: Aim 1: Develop poly-(OEGMA) substrates presenting controlled densities and patterns of cell adhesive ligands to modulate keratinocyte adhesion and morphology. Aim 2: Examine the effects of integrin-mediated adhesion to engineered substrates on keratinocyte proliferation and in vitro differentiation. Aim 3: Investigate the interactions between integrin-mediated adhesion and beta-catenin related pathways in the regulation epidermal differentiation. The successful completion of this research proposal will provide significant insights into the interacting roles of multiple pathways involved in the regulation of epidermal differentiation. The long term objective is to establish novel experimental systems that will improve the fundamental understanding of stem cell lineage selection, differentiation, and self renewal. This research has important implications in the field of cancer cell biology. Since integrin and beta-catenin signaling also influence tumor development and invasion, insights into the behavior of epidermal stem cells will advance the current understanding of skin cancer pathology and aid in the development of therapeutic agents.

描述（由申请人提供）：整合素介导的粘附在许多细胞过程中发挥核心作用，包括增殖、迁移和分化。在皮肤表皮内，整合素受体已知会影响干细胞分化；然而，ECM 信号与其他信号通路协调决定细胞命运的机制仍不清楚。本研究计划的总体目标是研究整合素介导的粘附和β-连环蛋白相关信号通路在表皮分化调节中的相互作用。拟议的研究将采用工程聚合物基质来控制呈现给细胞的细胞粘附配体的类型、密度和空间组织。将使用从野生型小鼠和具有诱导型 β-连环蛋白、Notch 和 c-Myc 表达的转基因小鼠分离的角质形成细胞来检查这些确定的细胞-基质相互作用对表皮分化的影响。这项工作的中心假设是，整合素介导的细胞外基质粘附调节角质形成细胞分化，并且这些反应受到β-连环蛋白信号传导和其他相关途径强度的调节。这项研究将围绕三个具体目标进行： 目标 1：开发具有受控密度和细胞粘附配体模式的聚（OEGMA）基质，以调节角质形成细胞粘附和形态。目标 2：检查整合素介导的工程基质粘附对角质形成细胞增殖和体外分化的影响。目标 3：研究整合素介导的粘附和 β-连环蛋白相关途径在调节表皮分化中的相互作用。该研究计划的成功完成将为了解表皮分化调节中涉及的多种途径的相互作用作用提供重要的见解。长期目标是建立新的实验系统，以提高对干细胞谱系选择、分化和自我更新的基本理解。这项研究在癌细胞生物学领域具有重要意义。由于整合素和β-连环蛋白信号传导也会影响肿瘤的发展和侵袭，因此对表皮干细胞行为的深入了解将增进目前对皮肤癌病理学的理解，并有助于治疗药物的开发。