Replenishment of the Innate Immune System

补充先天免疫系统

• 批准号: 7194603
• 负责人: Paul Wayne Kincade
• 金额: $ 27.13万
• 依托单位: OKLAHOMA MEDICAL RESEARCH FOUNDATION
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-09-25 至 2009-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7194603
• 关键词: Address; Animals; Anthrax disease; Antigens; Aorta; Attention; Autoimmune Process; Autoimmunity; Bacillus anthracis; Bacteria; Blood Cells; Bone Diseases; Bone Marrow; Categories; Cell Separation; Cells; Cellular biology; Cholesterol; Clostridium perfringens; Commit; Companions; Complex; Condition; Congenic Strain; Culture Techniques; Cultured Cells; Cytolysins; Dendritic Cells; Dependence; Differentiation and Growth; Discrimination; Disease; Effector Cell; Embryo; Experimental Designs; Exposure to; Family; Family member; Fetal Liver; Generations; Goals; Gonadal structure; Heating; Hematopoietic; Hematopoietic stem cells; Herpesviridae; Human; Immune system; Immunization; Individual; Infection; Influenza; Investigation; Knock-in Mouse; Knockout Mice; Learning; Life; Ligands; Long-Term Effects; Lymphocyte; Marrow; Mature Lymphocyte; Mediating; Mesonephric structure; Modeling; Monoclonal Antibodies; Mus; Mutate; Myelogenous; Organism; Pattern; Plants; Play; Population; Process; Production; Proliferating; Range; Research Personnel; Reverse Transcriptase Polymerase Chain Reaction; Signal Pathway; Signal Transduction; Site; Stem cells; Systemic infection; TLR2 gene; TLR4 gene; Testing; Thinking; Time; Toll-like receptors; Umbilical Cord Blood; Viral; Virus; autocrine; base; biodefense; bone; cell type; cytokine; in utero; in vivo; insight; killings; macrophage; microbial; neutralizing antibody; pathogen; perforin; preclinical study; progenitor; programs; receptor; research study; response; restoration; stem; transcription factor

DESCRIPTION (provided by applicant): Macrophages and dendritic cells are constantly replenished throughout life and represent important components of the innate immune system. They were long thought to be produced within bone marrow in strict dependence on growth and differentiation factors. However, our new findings suggest that a special mechanism comes into play during times of systemic infection. When stimulated in culture with ligands for the Toll-like receptors (TLR) but no other factors, highly purified hematopoietic cells give rise to macrophages and dendritic cells. TLR have attracted considerable attention because of their display on mature effector cells and their ability to recognize bacterial/viral products. Our preliminary results indicate that TLR are expressed on stem cells and provide a primitive but highly effective mechanism for producing cells of the innate immune system. This two year project will exploit special knock-in and congenic strains of mice together with cell sorting and culture techniques to determine precisely which stem and progenitor cells express functional TLR. Cells from mice and humans will be exposed to viruses, anthrax and bacterial products to learn the range of response patterns. Subsequent experiments will reveal how individual progenitors proliferate and differentiate when exposed to these substances, as well as how macrophage production can occur at the expense of other blood cell types. The project will progressively move from simple experimental designs to complex whole animal studies. The aim is to learn if infections skew normal differentiation patterns so that the innate immune system can be quickly restored. TLR bearing cells are being implicated in autoimmunity and a wide range of other diseases relevant to this new line of investigation. These studies are certain to provide fundamental information, but could also suggest new means to augment the innate immune system. Lay Summary: Even plants and simple organisms have some defense against disease, and use what is referred to as the "innate immune system". Humans are also protected by an innate immune system, and although it is not as sophisticated as that achieved with immunization, it can quickly sense and respond to bacteria and viruses. This project is based on an exciting discovery about how the innate immune system may be restored during infection. The findings may also suggest a way that bones and stem cells in the bone marrow are harmed by infections.

描述（由申请人提供）：巨噬细胞和树突细胞在整个生命过程中不断补充，是先天免疫系统的重要组成部分。长期以来，人们认为它们是在骨髓内产生的，严格依赖于生长和分化因子。然而，我们的新发现表明，在全身感染期间，一种特殊的机制发挥了作用。当在培养物中用 Toll 样受体 (TLR) 配体而不是其他因子刺激时，高度纯化的造血细胞会产生巨噬细胞和树突状细胞。 TLR 因其在成熟效应细胞上的展示以及识别细菌/病毒产物的能力而引起了相当大的关注。我们的初步结果表明，TLR 在干细胞上表达，并为产生先天免疫系统细胞提供了一种原始但高效的机制。这个为期两年的项目将利用特殊的基因敲入和同源小鼠品系以及细胞分选和培养技术来精确确定哪些干细胞和祖细胞表达功能性 TLR。来自小鼠和人类的细胞将暴露于病毒、炭疽和细菌产物，以了解反应模式的范围。随后的实验将揭示个体祖细胞在接触这些物质时如何增殖和分化，以及巨噬细胞的产生如何以牺牲其他血细胞类型为代价。该项目将逐步从简单的实验设计转向复杂的整体动物研究。目的是了解感染是否会扭曲正常的分化模式，以便先天免疫系统能够快速恢复。 TLR 承载细胞与自身免疫以及与这一新研究方向相关的多种其他疾病有关。这些研究肯定会提供基本信息，但也可能提出增强先天免疫系统的新方法。外行总结：即使是植物和简单的生物体也有一定的防御疾病的能力，并使用所谓的“先天免疫系统”。人类也受到先天免疫系统的保护，虽然它不像免疫系统那样复杂，但它可以快速感知细菌和病毒并做出反应。该项目基于一项关于如何在感染期间恢复先天免疫系统的令人兴奋的发现。这些发现还可能表明骨骼和骨髓中的干细胞受到感染损害的一种方式。