Dermatoremediation of Iron Overload

铁过量的皮肤修复

• 批准号: 7274872
• 负责人: LEONARD M MILSTONE
• 金额: $ 31.72万
• 依托单位: YALE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-12-01 至 2011-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7274872
• 关键词: Address; Blood; Blood Circulation; Body Burden; Breeding; Chelating Agents; Class; Cutaneous; DNA; Disease; Epidermis; Functional disorder; Funding; Genes; Genetic; Genetic Engineering; Goals; Hemochromatosis; Hereditary hemochromatosis; Homeostasis; Human; Hydroxamic Acids; Inflammatory; Ionophores; Iron; Iron Overload; Iron-Regulatory Proteins; Knockout Mice; Knowledge; Life; Liver; Measures; Methods; Modeling; Mus; Mutagenesis; Nifedipine; Organ; Papillomavirus Transforming Protein E7; Phototoxicity; Physiology; Porifera; Process; Protein Export Pathway; Rate; Regulation; Research Personnel; Response Elements; Retinoids; Risk; Role; SLC11A2 gene; Skin; Skin Cancer; Standards of Weights and Measures; Surface; Testing; Tissues; Topical application; Toxic effect; Toxin; Transferrin; Transferrin Receptor; Transgenes; Transgenic Mice; Translating; UVB induced; Work; base; chemical carcinogenesis; design; divalent metal; expectation; hepcidin; human WNT2 protein; involucrin; keratinocyte; metal transporting protein 1; mouse model; neoplastic; novel strategies; programs; research study; skin disorder; tool

DESCRIPTION (provided by applicant): The goal of this work is to demonstrate that the normal process of epidermal desquamation can be harnessed to eliminate systemic toxins from the body. This proposal focuses on iron as a model toxin. Iron is essential for life, but too much iron causes the disease hemochromatosis. Normally, 20% of absorbed iron is eliminated through epidermal desquamation. The central hypothesis is that if epidermis can be made to act as a sink for internal iron, then epidermal shedding might reduce the body burden of iron. AIM I. tests the feasibility of this approach by experiments designed to reduce the systemic iron burden in the Hfe null mouse model of heriditary hemochromatosis. A. We will cause epidermis to act as a sink or sponge for iron and then measure the effect on iron stores in internal organs: 1. by breeding experiments leading to over-expression of the transferrin receptor in epidermis; 2. by topical application of iron ionophores or iron chelators; B. We will accelerate cutaneous iron loss through increased epidermal turnover and desquamation: 1. by breeding experiments leading to over-expression of the viral E7 protein in epidermis; 2. by systemic administration of a synthetic retinoid; AIM II investigates the physiology and pathophysiology of iron in mouse keratinocyte cultures and in mouse epidermis. The goal is to identify better ways of causing epidermis to act as a sink for iron and to test whether elevated iron in epidermis is toxic. A. We will identify additional ways to increase iron accumulation in epidermis 1. by characterizing expression and function of iron export protein ferroportin in epidermis; 2. by using hepcidin to regulate expression of ferroportin; B. We will evaluate whether epidermal iron increases the risk for phototoxicity, DNA mutagenesis or skin cancer, using our transgenic mice in which iron accumulation is restricted to epidermis. Relevance: This proposal represents a novel approach to the elimination of systemic toxins by causing them to be shed from the skin surface. By focusing on iron, it also will provide basic new information to fill existing gaps in knowledge about the physiology and pathophysiology of iron in the epidermis. Since iron is increasingly suspected of having a role in inflammatory and neoplastic diseases of skin, this new information should assist in devising preventative and treatment measures for those types of diseases.

描述（由申请人提供）：这项工作的目的是证明可以利用正常的表皮脱屑过程来消除体内的全身毒素。这一建议的重点是铁作为一种模型毒素。铁是生命所必需的，但过量的铁会导致血色素沉着症。正常情况下，20%被吸收的铁通过表皮脱屑排出。核心假设是，如果表皮可以作为内部铁的水槽，那么表皮脱落可能会减少身体的铁负担。