实验动物与比较医学 ›› 2016, Vol. 36 ›› Issue (6): 473-478.DOI: 10.3969/j.issn.1674-5817.2016.06.014

• 综述 • 上一篇    下一篇

TX 小鼠研究进展

张薇, 唐彬, 黎福荣   

  1. 中山大学实验动物中心, 广州 510080
  • 收稿日期:2016-08-25 出版日期:2016-12-25 发布日期:2016-12-25
  • 作者简介:张薇(1964-), 女, 高级实验师, 硕士, 从事中西医结合基础和实验动物研究工作。E-mail: zwygqj@163.com
  • 基金资助:
    广东省科技基础条件建设项目(No: 2013B060300010)

Research Progress on Toxic Milk Mouse

ZHANG Wei, TANG Bin, LI Fu-rong   

  1. Laboratory Animal Center of Sun Yat-sen University, Guangzhou 510080, China
  • Received:2016-08-25 Online:2016-12-25 Published:2016-12-25

摘要: TX 小鼠(toxic milk mouse)是由DL近交系小鼠繁殖到第68 代所产生的自然突变品系。主要表现为低色素化、生长迟缓、震颤和运动功能障碍等,其与Wilson 病的共同点包括: 遗传方式属于常染色体隐性遗传、成年小鼠体内铜大量沉积使血清铜和血清铜蓝蛋白水平降低等特点。文 章从TX 小鼠的病理生理学、致病机理、病理治疗学等多个方面综述了TX小鼠的研究现状。

关键词: TX 小鼠, 铜离子积累, ATP7B 蛋白

Abstract: Toxic milk mouse is mutant a strain that produced by DL mice at F68. The main pathological shows are low pigmentation, growth retardation, tremor and movement disturbance. The common ground with Wilson disease are autosomal recessive inheritance, and large quantities of copper deposit in adult mouse that lead the levels of serum copper and serum ceruloplasmin protein declined. This paper reviews the researches on Toxic milk from several aspects, including pathophysiology, disease mechanism, diagnostics and therapy.

Key words: Toxic milk mouse, Accumulation of copper, Protein ATP7B

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