Ha Seungmin, Lee Dongwon, Cho Yi Sul, Chung Changuk, Yoo Ye-Eun, Kim Jihye, Lee Jiseok, Kim Woohyun, Kim Hyosang, Bae Yong Chul, Tanaka-Yamamoto Keiko, Kim Eunjoon
Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon 305-701, Korea.
Center for Synaptic Brain Dysfunctions, Institute for Basic Science, Daejeon 305-701, Korea.
J Neurosci. 2016 Nov 30;36(48):12129-12143. doi: 10.1523/JNEUROSCI.1849-16.2016.
Shank2 is a multidomain scaffolding protein implicated in the structural and functional coordination of multiprotein complexes at excitatory postsynaptic sites as well as in psychiatric disorders, including autism spectrum disorders. While Shank2 is strongly expressed in the cerebellum, whether Shank2 regulates cerebellar excitatory synapses, or contributes to the behavioral abnormalities observed in Shank2 mice, remains unexplored. Here we show that Shank2 mice show reduced excitatory synapse density in cerebellar Purkinje cells in association with reduced levels of excitatory postsynaptic proteins, including GluD2 and PSD-93, and impaired motor coordination in the Erasmus test. Shank2 deletion restricted to Purkinje cells (Pcp2-Cre;Shank2 mice) leads to similar reductions in excitatory synapse density, synaptic protein levels, and motor coordination. Pcp2-Cre;Shank2 mice do not recapitulate autistic-like behaviors observed in Shank2 mice, such as social interaction deficits, altered ultrasonic vocalizations, repetitive behaviors, and hyperactivity. However, Pcp2-Cre;Shank2 mice display enhanced repetitive behavior in the hole-board test and anxiety-like behavior in the light-dark test, which are not observed in Shank2 mice. These results implicate Shank2 in the regulation of cerebellar excitatory synapse density, motor coordination, and specific repetitive and anxiety-like behaviors.
The postsynaptic side of excitatory synapses contains multiprotein complexes, termed the postsynaptic density, which contains receptors, scaffolding/adaptor proteins, and signaling molecules. Shank2 is an excitatory postsynaptic scaffolding protein implicated in the formation and functional coordination of the postsynaptic density and has been linked to autism spectrum disorders. Using Shank2-null mice and Shank2-conditional knock-out mice with a gene deletion restricted to cerebellar Purkinje cells, we explored functions of Shank2 in the cerebellum. We found that Shank2 regulates excitatory synapse density, motor coordination, and specific repetitive and anxiety-like behaviors, but is not associated with autistic-like social deficits or repetitive behaviors.
Shank2是一种多结构域支架蛋白,参与兴奋性突触后位点多蛋白复合物的结构和功能协调,以及包括自闭症谱系障碍在内的精神疾病。虽然Shank2在小脑中强烈表达,但Shank2是否调节小脑兴奋性突触,或是否导致Shank2基因敲除小鼠中观察到的行为异常,仍未得到探索。在这里,我们表明,Shank2基因敲除小鼠小脑浦肯野细胞中的兴奋性突触密度降低,同时兴奋性突触后蛋白水平降低,包括GluD2和PSD - 93,并在伊拉斯谟试验中运动协调性受损。仅限于浦肯野细胞的Shank2基因缺失(Pcp2 - Cre;Shank2小鼠)导致兴奋性突触密度、突触蛋白水平和运动协调性出现类似降低。Pcp2 - Cre;Shank2小鼠并未重现Shank2基因敲除小鼠中观察到的自闭症样行为,如社交互动缺陷、超声波发声改变、重复行为和多动。然而,Pcp2 - Cre;Shank2小鼠在洞板试验中表现出增强的重复行为,在明暗试验中表现出焦虑样行为,而这些在Shank2基因敲除小鼠中未观察到。这些结果表明Shank2参与调节小脑兴奋性突触密度、运动协调性以及特定的重复和焦虑样行为。
兴奋性突触的突触后侧包含多蛋白复合物,称为突触后致密物,其中包含受体、支架/衔接蛋白和信号分子。Shank2是一种兴奋性突触后支架蛋白,参与突触后致密物的形成和功能协调,并与自闭症谱系障碍有关。使用Shank2基因敲除小鼠和仅限于小脑浦肯野细胞基因缺失的Shank2条件性敲除小鼠,我们探索了Shank2在小脑中的功能。我们发现Shank2调节兴奋性突触密度、运动协调性以及特定的重复和焦虑样行为,但与自闭症样社交缺陷或重复行为无关。