GENETIC SUSCEPTIBILITY TO GRAVES'-LIKE HYPERTHYROIDISM IN MICE

小鼠对格雷夫斯样甲状腺功能亢进症的遗传易感性

• 批准号: 8100177
• 负责人: Sandra M McLachlan
• 金额: $ 33.9万
• 依托单位: CEDARS-SINAI MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-07-01 至 2015-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8100177
• 关键词: Adenoviruses; Affect; Animal Model; Antibodies; Antibody Formation; Autoantibodies; Binding; Brothers; Chinese Hamster Ovary Cell; Chromosomes; Chromosomes, Human, Pair 17; Data; Data Linkages; Databases; Development; Disease; Enzyme-Linked Immunosorbent Assay; Future; Generations; Genes; Genetic; Genetic Predisposition to Disease; Genotype; Goals; Health; Human; Human Genome; Hyperthyroidism; Immune Response Genes; Immunity; Immunization; Immunoglobulins; Inbred Mouse; Inbreeding; Light; Link; Measures; Modeling; Mouse Strains; Mus; Nature; Parents; Patients; Play; Predisposition; Recombinant Inbred Strain; Recombinants; Regulatory T-Lymphocyte; Resistance; Role; Serum; Sister; Stratification; Thyroid Function Tests; Thyroid Gland; Thyroid Hormones; Thyroid stimulating immunoglobulins; Thyrotropin Receptor; Thyroxine; Variant; Woman; base; genetic linkage analysis; genome wide association study; genome-wide; insight; trait

DESCRIPTION (provided by applicant): Graves' hyperthyroidism is caused by thyroid stimulating autoantibodies (TSAb) to the thyrotropin receptor (TSHR). Some mouse strains are susceptible, and some are resistant, to developing hyperthyroidism induced by TSHR- adenovirus immunization. This difference permits analyzing the genetic susceptibility to hyperthyroidism in mice. Recombinant inbred (RI) mice are stable lines derived by repeated brother x sister matings of the progeny of two strains. Our studies in genotyped CXB and BXH RI strains revealed that induced TSHR antibodies and hyperthyroidism are influenced by different chromosomal loci. We will build on these findings as follows: 1. Genetic controlofthyroidbaseline parameters and responsiveness to stimulation : To obtain insight into the genetic susceptibility for these parameters, we will study RI mice derived from parental strains differing in serum T4 and Tg values by: Determining T4 and Tg levels at baseline and after TSH stimulation in BXH and BXD RI sets of mice. Performing linkage analysis to identify chromosomes and loci responsible for variability in T4, Tg and TSH. 2. TSHR antibodies as a measure of immunity to the TSHR . AXB/BXA and DXB RI mice, derived fromparental strains differing in TSHR antibody responses (A versus B6 and DBA/2 versus B6 for the two RI sets, respectively) will be immunized with TSHR-adenovirus to: Determine induced TSHR antibody levels measured as TSH binding inhibition, TSAb and ELISA. TSAb bioactivity will be compared using CHO cells expressing human and mouse TSHR. Identify by linkage analysis the chromosomes/loci associated with these traits. 3. Susceptibility to hyperthyroidism induced by thyroid stimulating antibodies (TSAb). We will perform the following studies: Immunize AXB/BXA and BXD sets of RI mice with TSHR-adenovirus. To overcome resistance to induced hyperthyroidism in BXD mice, we will deplete Treg before TSHR-adenovirus immunization. Determine chromosomes/loci influencing iantibody induced hyperthyroidism in AXB/BXA and BXD strains. Overall, these studies in mice will provide the basis for future studies refining genetic loci and provide insight into approaches for phenotypic stratification of Graves' patients in human genome wide array analyses PUBLIC HEALTH RELEVANCE: Graves' hyperthyroidism is caused by thyroid stimulating antibodies to the thyrotropin receptor (TSHR) that mimic stimulation by TSH. The disease is multigenic but genome wide scans in large patient groups fail to reveal common genes except for MHC. We will use an induced model of Graves' hyperthyroidism in genetically typed inbred mice to establish the genetic basis for the development of TSHR antibodies and elevated serum thyroxine with the goal of providing insight into subsetting Graves' patients for future human genome wide array analyses.

描述(申请人提供)：Graves‘s甲亢是由促甲状腺激素受体(TSHR)的甲状腺刺激性自身抗体(TSAb)引起的。一些小鼠品系对TSHR-腺病毒免疫引起的甲状腺功能亢进症敏感，一些品系具有抵抗力。这种差异使得分析小鼠甲亢的遗传易感性成为可能。重组近交系(RI)小鼠是由两个品系的后代重复交配而成的稳定品系。我们对CXB和BXH RI株基因分型的研究表明，诱导的TSHR抗体和甲亢受不同染色体位点的影响。我们将以这些研究结果为基础，总结如下： 1.甲状腺基线参数和刺激反应性的遗传控制：为了深入了解这些参数的遗传易感性，我们将研究来自不同血清T4和TG值亲本品系的RI小鼠：测定BXH和BXD RI小鼠在基线和TSH刺激后的T4和TG水平。进行连锁分析以确定导致T4、TG和TSH变异的染色体和基因座。2.TSHR抗体作为TSHR免疫力的一种指标。用TSHR-腺病毒免疫AXB/BXA和DXB RI小鼠，测定诱导的TSHR抗体水平，包括TSH结合抑制、TSAb和EL ISA。TSAb生物活性将用表达人和小鼠TSHR的CHO细胞进行比较。通过连锁分析确定与这些性状相关的染色体/基因座。3.甲状腺刺激性抗体(TSAb)对甲亢的易感性。我们将进行以下研究：用TSHR-腺病毒免疫RI小鼠AXB/BXA和BXD组。为了克服BXD小鼠对诱导甲亢的抵抗力，我们将在TSHR-腺病毒免疫之前去除Treg。确定AXB/BXA和BXD菌株中影响抗体诱导的甲状腺功能亢进的染色体/基因座。总体而言，这些对小鼠的研究将为未来精炼遗传基因座的研究提供基础，并为人类基因组宽阵列分析中Graves病患者的表型分层提供洞察力。 与公共卫生相关：Graves‘s甲亢是由促甲状腺激素受体(TSHR)的甲状腺刺激性抗体引起的，TSHR模仿TSH的刺激。这种疾病是多基因的，但在大型患者群体中进行全基因组扫描时，除了MHC之外，无法发现共同的基因。我们将使用遗传型近交系小鼠Graves‘s甲亢的诱导模型，为TSHR抗体的开发和血清甲状腺激素的升高建立遗传学基础，目的是为未来的人类基因组全阵列分析提供对Graves’s患者亚型的洞察力。