H2 haplotype and atherosclerosis

H2单倍型与动脉粥样硬化

• 批准号: 8399045
• 负责人: WEIBIN SHI
• 金额: $ 18.33万
• 依托单位: UNIVERSITY OF VIRGINIA
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-12-15 至 2015-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8399045
• 关键词: 6p21.3; Accounting; Affect; Aorta; Apolipoprotein E; Apolipoproteins B; Apoptosis; Arterial Fatty Streak; Atherogenic Diet; Atherosclerosis; Bone Marrow Transplantation; C3H/HeJ Mouse; Candidate Disease Gene; Cell Cycle Arrest; Cell Wall; Centromere; Chromosomal Instability; Chromosomes, Human, Pair 17; Chromosomes, Human, Pair 6; Chronic; Code; Congenic Strain; DNA; DNA Damage; DNA Double Strand Break; DNA Repair; DNA damage checkpoint; DNA-PKcs; Defect; Development; Disease; Docking; Enzymes; Exhibits; Foam Cells; Gene Targeting; Genes; Genetic Determinism; Genetic Variation; Genome Components; Genotype; H2AFX gene; HLA Antigens; Haplotypes; Human; Hypersensitivity; Inbred C3H Mice; Inbred Strain; Inflammation; Inflammatory; Ionizing radiation; KRP protein; Lesion; Light; Link; Lipoproteins; Low-Density Lipoproteins; Major Histocompatibility Complex; Mammalian Cell; Mediator of activation protein; Modality; Mus; Non-Malignant; Nucleic Acid Regulatory Sequences; Pathway interactions; Patients; Phosphatidylinositols; Phosphotransferases; Play; Predisposition; Proliferating; Protein Kinase; Proteins; Pulmonary Fibrosis; Radiation; Radiation therapy; Reactive Oxygen Species; Relative (related person); Resistance; Resources; Risk; Risk Factors; Role; Site; Testing; Tissues; arm; cancer therapy; cytokine; feeding; gene induction; irradiation; low density lipoprotein inhibitor; macrophage; monocyte; mouse model; novel; oxidized low density lipoprotein; response; surveillance network

DESCRIPTION (provided by applicant): Radiation is a risk factor for atherosclerotic cardiovascular disease. However, little is known about the mechanisms that underlie radiation-enhanced atherosclerosis. Our recent studies have identified H2, the murine MHC, as a major genetic determinant of susceptibility to radiation-enhanced atherosclerosis. C3H/HeJ (C3H) mice are extremely resistant to atherosclerosis, developing much smaller lesions than C57BL/6 (B6) mice when deficient in apolipoprotein E (apoE-/-) or fed an atherogenic diet. The two strains differ in the H2 haplotype with B6 having H2b and C3H having H2k. C3.SW-H2b/SnJ (C3.SW) is a congenic strain of C3H/HeJ in which the H2k locus is replaced with H2b. Surprisingly, C3.SW.apoE-/- mice that underwent bone marrow transplantation after lethal irradiation exhibited a 21-fold increase in atherosclerotic lesion size relative to C3H.apoE-/- mice receiving the same treatment, demonstrating the dramatic impact of H2 haplotypes on atherosclerosis. We will use this novel C3.SW.apoE-/- mouse model to investigate mechanistic links between H2 haplotypes and plaque formation. We will also test a promising candidate gene in the H2 region. MDC1, encoding the mediator of DNA damage checkpoint 1, is a component of the genome surveillance network activated by DNA double-strand breaks. Multiple SNPs have been detected in both coding and regulatory regions of MDC1 between H2b and H2k haplotypes. We will determine whether deficiency in MDC1 would promote atherosclerosis following radiation. These studies will shed light on new genes and new pathways that control atherosclerosis susceptibility.

描述（由申请方提供）：辐射是动脉粥样硬化性心血管疾病的风险因素。然而，对辐射增强动脉粥样硬化的机制知之甚少。我们最近的研究已经确定了H2，小鼠MHC，作为一个主要的遗传因素的易感性辐射增强动脉粥样硬化。C3 H/HeJ（C3 H）小鼠对动脉粥样硬化具有极强的抵抗力，当缺乏载脂蛋白E（apoE-/-）或喂食致动脉粥样硬化饮食时，其病变比C57 BL/6（B6）小鼠小得多。这两个菌株在H2单倍型上不同，B6具有H2 b，C3 H具有H2k。C3. SW-H2 b/SnJ（C3.SW）是C3 H/HeJ的同源株，其中H2k位点被H2 b替换。令人惊讶的是，C3.SW.apoE-/-小鼠接受骨髓移植后，致命的辐射表现出动脉粥样硬化病变的大小增加了21倍，相对于C3H.apoE-/-小鼠接受相同的治疗，证明了显着的影响H2单倍型动脉粥样硬化。我们将使用这种新的C3.SW.apoE-/-小鼠模型来研究H2单倍型和斑块形成之间的机制联系。我们还将在H2区域测试一个有希望的候选基因。MDC 1编码DNA损伤检查点1的介质，是由DNA双链断裂激活的基因组监视网络的组成部分。在H2 b和H2k单倍型之间的MDC 1编码区和调控区检测到多个SNP。我们将确定MDC 1的缺乏是否会促进辐射后的动脉粥样硬化。这些研究将揭示控制动脉粥样硬化易感性的新基因和新途径。