Phenotype of the taurine transporter knockout mouse

被引:123
作者
Warskulat, Ulrich [1 ]
Heller-Stilb, Birgit
Oermann, Evelyn
Zilles, Karl
Haas, Helmut
Lang, Florian
Haeussinger, Dieter
机构
[1] Univ Dusseldorf, Clin Gastroenterol Hepatol & Infectiol, D-4000 Dusseldorf, Germany
[2] Univ Dusseldorf, Vogt Inst Brain Res, C & O, D-4000 Dusseldorf, Germany
[3] Res Ctr, Inst Med, Julich, Germany
[4] Univ Dusseldorf, Dept Neurophysiol, D-4000 Dusseldorf, Germany
[5] Univ Tubingen, Dept Physiol, D-72074 Tubingen, Germany
来源
OSMOSENSING AND OSMOSIGNALING | 2007年 / 428卷
关键词
D O I
10.1016/S0076-6879(07)28025-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This chapter reports present knowledge on the properties of mice with disrupted gene coding for the taurine transporter (taut-/- mice). Study of those mice unraveled some of the roles of taurine and its membrane transport for the development and maintenance of normal organ functions and morphology. When compared with wild-type controls, taut-/- mice have decreased taurine levels in skeletal and heart muscle by about 98%, in brain, kidney, plasma, and retina by 80 to 90%, and in liver by about 70%. taut-/- mice exhibit a lower body mass as well as a strongly reduced exercise capacity compared with taut+/- and wild-type mice. Furthermore, taut-/- mice show a variety of pathological features, for example, subtle derangement of renal osmoregulation, changes in neuroreceptor expression, and loss of long-term potentiation in the striatum, and they develop clinically relevant age-dependent disorders, for example, visual, auditory, and olfactory dysfunctions, unspecific hepatitis, and liver fibrosis.
引用
收藏
页码:439 / +
页数:22
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