Department of Anatomy and Neurobiology, University of Maryland School of Medicine , Baltimore, Maryland 21201.
eNeuro. 2014 Nov 12;1(1). doi: 10.1523/ENEURO.0007-14.2014. eCollection 2014 Nov-Dec.
Cover FigureRegion-specific adenylyl cyclase 1 (AC1) loss of function differentially affects both patterning and sensorimotor behaviors in mice. AC1 is expressed at all levels of the somatosensory pathway and plays a major role in refinement and patterning of topographic sensory maps. Cortex-specific AC1 loss of function (CxAC1KO mice) does not affect barrel patterning and activation of specific barrels corresponding to stimulated whiskers and does not impair sensorimotor behaviors. While global (AC1KO) and thalamus-specific (ThAC1KO) AC1 loss of function leads to absence of barrel patterns, selective whisker stimulation activates topographically aligned cortical loci. Despite functional topography of the whisker-barrel cortex, sensorimotor and social behaviors are impaired, indicating the importance of patterning of topographical sensory maps in the neocortex. Adenylate cyclase type I (AC1) is primarily, and, abundantly, expressed in the brain. Intracellular calcium/calmodulin increases regulate AC1 in an activity-dependent manner. Upon stimulation, AC1 produces cAMP and it is involved in the patterning and the refinement of neural circuits. In mice, spontaneous mutations or targeted deletion of the Adcy1 gene, which encodes AC1, resulted in neuronal pattern formation defects. Neural modules in the primary somatosensory (SI) cortex, the barrels, which represent the topographic distribution of the whiskers on the snout, failed to form (Welker et al., 1996; Abdel-Majid et al., 1998). Cortex- or thalamus-specific Adcy1 deletions led to different cortical pattern phenotypes, with thalamus-specific disruption phenotype being more severe (Iwasato et al., 2008; Suzuki et al., 2013). Despite the absence of barrels in the "barrelless"/Adcy1 null mice, thalamocortical terminal bouton density and activation of cortical zones following whisker stimulation were roughly topographic (Abdel-Majid et al., 1998; Gheorghita et al., 2006). To what extent does patterning of the cortical somatosensory body map play a role in sensorimotor behaviors? In this study, we tested mice with global, cortical, or thalamic loss of AC1 function in a battery of sensorimotor and social behavior tests and compared them to mice with all of the whiskers clipped. Contrary to intuitive expectations that any region-specific or global disruption of the AC1 function would lead to similar behavioral phenotypes, we found significant differences in the degree of impairment between these strains.
封面图片区域特异性腺苷酸环化酶 1(AC1)功能丧失会对小鼠的模式形成和感觉运动行为产生不同的影响。AC1 在感觉通路的各个水平表达,在感觉图谱的细化和模式形成中起主要作用。皮层特异性 AC1 功能丧失(CxAC1KO 小鼠)不会影响桶状结构的形成和对应刺激胡须的特定桶的激活,也不会损害感觉运动行为。虽然全局(AC1KO)和丘脑特异性(ThAC1KO)AC1 功能丧失导致桶状结构缺失,但选择性胡须刺激会激活具有地形排列的皮质位置。尽管在感觉运动皮层中存在功能拓扑结构,但感觉运动和社交行为受损,这表明在新皮层中,拓扑感觉图谱的模式形成对其非常重要。腺苷酸环化酶 1 型(AC1)主要且丰富地表达于大脑中。细胞内钙/钙调蛋白增加以活动依赖性方式调节 AC1。受到刺激时,AC1 会产生 cAMP,它参与了神经回路的模式形成和细化。在小鼠中,Adcy1 基因(编码 AC1)的自发突变或靶向缺失导致神经元模式形成缺陷。初级躯体感觉(SI)皮层中的神经模块,即代表鼻子上胡须的拓扑分布的桶状结构,未能形成(Welker 等人,1996 年;Abdel-Majid 等人,1998 年)。皮层或丘脑特异性 Adcy1 缺失导致不同的皮层模式表型,其中丘脑特异性破坏表型更为严重(Iwasato 等人,2008 年;Suzuki 等人,2013 年)。尽管“无桶状结构”/Adcy1 缺失小鼠中不存在桶状结构,但在胡须刺激后,丘脑皮质终末末梢的密度和皮质区域的激活大致具有地形特征(Abdel-Majid 等人,1998 年;Gheorghita 等人,2006 年)。皮质躯体感觉图谱的模式形成在感觉运动行为中起到何种程度的作用?在这项研究中,我们在一系列感觉运动和社交行为测试中测试了具有全局、皮层或丘脑 AC1 功能丧失的小鼠,并将它们与所有胡须被剪掉的小鼠进行了比较。与直觉相反,我们发现这些品系之间的损伤程度存在显著差异,任何区域特异性或全局的 AC1 功能障碍都不会导致类似的行为表型。