首页> 外文期刊>Journal de la Societe de biologie >Interet des modeles animaux pour I'etude des pathologies humaines : exemple d'un modele de souris pour la trisomie 21
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Interet des modeles animaux pour I'etude des pathologies humaines : exemple d'un modele de souris pour la trisomie 21

机译:动物模型对人类病理学研究的兴趣:21三体模型的小鼠模型示例

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Relevance of animal models in the study of human pathologies: a mouse model of Down syndrome.Animal models provide a simplified representation of biological systems impossible to study directly in the human being. Regarding genetic pathologies, mouse models are the most studied since they enable to reproduce in animals the mutation of the gene or genes responsible for the disease and to study the phenotypic consequences. Down syndrome is a genetic disorder arising from the presence of a third copy of the human chromosome 21 (Hsa21) and is characterized by different degrees of phenotypic alterations including morphological, cardiac, muscular, cerebral, motor and intellectual changes. This high phenotypic heterogeneity involves genetic and environmental effects, which are impossible to dissect out in human beings. Various models in mice have been developed in order to identify the genetic and neurobiological mechanisms responsible for Down syndrome. The Tel mouse is the most complete genetic animal model currently available to study Down syndrome, since it carries an almost complete Hsa 21. The behavioural and electrophysiological studies of this model reveal a great similarity between the animal phenotype and the Down syndrome symptomatology, consequently this model represents a powerful genetic tool with a potential to unravel the mechanisms underlying the deficiencies array characteristic of this human condition. In the long term, Tel mice will contribute to the development and the screening of new therapeutics, with the goal of improving all the impairments reported in Down syndrome.
机译:动物模型在人类病理学研究中的相关性:唐氏综合症的小鼠模型。动物模型提供了无法直接在人类中研究的生物系统的简化表示。关于遗传病理学,对小鼠模型的研究最多,因为它们能够在动物体内复制引起该疾病的一种或多种基因的突变并研究表型的后果。唐氏综合症是由人类第21号染色体第三个副本(Hsa21)引起的遗传疾病,其特征是不同程度的表型改变,包括形态,心脏,肌肉,大脑,运动和智力变化。这种高表型异质性涉及遗传和环境影响,这在人类中是不可能分解的。为了确定造成唐氏综合症的遗传和神经生物学机制,已经开发了多种小鼠模型。 Tel小鼠是目前可用于研究唐氏综合症的最完整的遗传动物模型,因为它携带了几乎完整的Hsa21。此模型的行为和电生理研究表明,动物表型与唐氏综合症的症状之间有很大的相似性,因此该模型代表了一种强大的遗传工具,具有揭示这种人类状况缺陷阵列特征的潜在机制的潜力。从长远来看,Tel小鼠将有助于开发和筛选新的治疗药物,目的是改善唐氏综合症中报道的所有损伤。

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