Characterization of Rett Syndrome-like phenotypes in Mecp2-knockout rats

被引:43
作者
Wu, Yang [1 ]
Zhong, Weiwei [1 ]
Cui, Ningren [1 ]
Johnson, Christopher M. [1 ]
Xing, Hao [1 ]
Zhang, Shuang [1 ]
Jiang, Chun [1 ]
机构
[1] Georgia State Univ, Dept Biol, 50 Decatur St, Atlanta, GA 30302 USA
关键词
Mecp2-null rat; Rett syndrome; Behaviors; Breathing; Locus coeruleus; LOCUS-COERULEUS NEURONS; MOUSE MODEL; MECP2-NULL MICE; FUNCTIONAL NEUROANATOMY; RESPIRATORY NETWORK; AUTISM; DYSFUNCTION; DEFICIENCY; DISORDERS; INACTIVATION;
D O I
10.1186/s11689-016-9156-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Rett Syndrome (RTT) is a neurodevelopmental disease caused by the disruption of the MECP2 gene. Several mouse models of RTT have been developed with Mecp2 disruptions. Although the mouse models are widely used in RTT research, results obtained need to be validated in other species. Therefore, we performed these studies to characterize phenotypes of a novel Mecp2(-/Y) rat model and compared them with the Mecp2(tm1.1Bird) mouse model of RTT. Methods: RTT-like phenotypes were systematically studied and compared between Mecp2(-/Y) rats and Mecp2(-/Y) mice. In-cage conditions of the rats were monitored. Grip strength and spontaneous locomotion were used to evaluate the motor function. Three-chamber test was performed to show autism-type behaviors. Breathing activity was recorded with the plethysmograph. Individual neurons in the locus coeruleus (LC) were studied in the whole-cell current clamp. The lifespan of the rats was determined with their survival time. Results: Mecp2(-/Y) rats displayed growth retardation, malocclusion, and lack of movements, while hindlimb clasping was not seen. They had weaker forelimb grip strength and a lower rate of locomotion than the WT littermates. Defects in social interaction with other rats were obvious. Breathing frequency variation and apnea in the null rats were significantly higher than in the WT. LC neurons in the null rats showed excessive firing activity. A half of the null rats died in 2 months. Most of the RTT-like symptoms were comparable to those seen in Mecp2(-/Y) mice, while some appeared more or less severe. The findings that most RTT-like symptoms exist in the rat model with moderate variations and differences from the mouse models support the usefulness of both Mecp2(-/Y) rodent models. Conclusions: The novel Mecp2(-/Y) rat model recapitulated numerous RTT-like symptoms as Mecp2(-/Y) mouse models did, which makes it a valuable alternative model in the RTT studies when the body size matters.
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页数:12
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