Concerted roles of LRRTM1 and SynCAM 1 in organizing prefrontal cortex synapses and cognitive functions

被引:20
作者
de Arce, Karen Perez [1 ,6 ]
Ribic, Adema [1 ,7 ]
Chowdhury, Dhrubajyoti [2 ]
Watters, Katherine [1 ,2 ]
Thompson, Garth J. J. [3 ,8 ]
Sanganahalli, Basavaraju G. G. [3 ]
Lippard, Elizabeth T. C. [3 ,9 ]
Rohlmann, Astrid [4 ]
Strittmatter, Stephen M. M. [2 ,5 ]
Missler, Markus [4 ]
Hyder, Fahmeed [3 ]
Biederer, Thomas [1 ,2 ]
机构
[1] Tufts Univ, Dept Neurosci, Sch Med, Boston, MA 02155 USA
[2] Yale Sch Med, Dept Neurol, New Haven, CT 06510 USA
[3] Yale Sch Med, Dept Radiol & Biomed Imaging, New Haven, CT USA
[4] Westfal Wilhelms Univ, Inst Anat & Mol Neurobiol, Munster, Germany
[5] Yale Sch Med, Dept Neurosci, New Haven, CT USA
[6] Novartis Inst Biomed Res, Neurosci Dept, Cambridge, MA USA
[7] Univ Virginia, Dept Psychol, Charlottesville, VA USA
[8] ShanghaiTech Univ, iHuman Inst, Shanghai, Peoples R China
[9] Univ Texas Austin, Dept Psychiat, Austin, TX USA
关键词
RESTING-STATE FMRI; CORTICAL PYRAMIDAL NEURONS; SYNAPTIC ADHESION MOLECULE; DENDRITIC SPINE PATHOLOGY; GLOBAL SIGNAL; NEUREXIN LIGANDS; RAT-BRAIN; SCHIZOPHRENIA; PLASTICITY; CONNECTIVITY;
D O I
10.1038/s41467-023-36042-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
LRRTM1 is a post synaptic adhesion protein, that promotes AMPA receptor mediated synaptic transmission. Here the authors show that LRRTM1 and the adhesion molecule SynCAM 1 act together to organize synapses in the prefrontal cortex with relevance for cognitive function in mice. Multiple trans-synaptic complexes organize synapse development, yet their roles in the mature brain and cooperation remain unclear. We analyzed the postsynaptic adhesion protein LRRTM1 in the prefrontal cortex (PFC), a region relevant to cognition and disorders. LRRTM1 knockout (KO) mice had fewer synapses, and we asked whether other synapse organizers counteract further loss. This determined that the immunoglobulin family member SynCAM 1 controls synapse number in PFC and was upregulated upon LRRTM1 loss. Combined LRRTM1 and SynCAM 1 deletion substantially lowered dendritic spine number in PFC, but not hippocampus, more than the sum of single KO impairments. Their cooperation extended presynaptically, and puncta of Neurexins, LRRTM1 partners, were less abundant in double KO (DKO) PFC. Electrophysiology and fMRI demonstrated aberrant neuronal activity in DKO mice. Further, DKO mice were impaired in social interactions and cognitive tasks. Our results reveal concerted roles of LRRTM1 and SynCAM 1 across synaptic, network, and behavioral domains.
引用
收藏
页数:18
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