Genetic and cognitive windows into circuit mechanisms of psychiatric disease

被引:50
作者
Arguello, P. Alexander [3 ,4 ]
Gogos, Joseph A. [1 ,2 ]
机构
[1] Columbia Univ, Dept Neurosci, New York, NY 10032 USA
[2] Columbia Univ, Dept Physiol & Cellular Biophys, New York, NY 10032 USA
[3] Princeton Univ, Princeton Neurosci Inst, Princeton, NJ 08544 USA
[4] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
关键词
AUTISM SPECTRUM DISORDERS; SHORT-TERM PLASTICITY; HIPPOCAMPAL SYNAPTIC PLASTICITY; COPY NUMBER VARIATION; FMR1 KNOCKOUT MICE; FRAGILE-X-SYNDROME; WORKING-MEMORY; PREFRONTAL CORTEX; MOUSE MODEL; TOP-DOWN;
D O I
10.1016/j.tins.2011.11.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Accumulating evidence indicates substantial etiological and pathophysiological heterogeneity as well as overlap within and across psychiatric disorders. Moreover, it is uncertain at what level, besides gross behavior, mental illnesses can be differentiated. To advance our understanding of psychiatric disease, we advocate a more systematic approach in characterizing a small number of animal models by utilizing unequivocal rare disease mutations and targeted cognitive assessment to identify convergent disease circuits and mechanisms. Based on available data, we discuss the possibility that the temporal dynamics of synaptic plasticity play a central role in disease pathophysiology and that the extent and manner in which they are altered in specific neural circuits determine the exact clinical phenotype of diverse disorders.
引用
收藏
页码:3 / 13
页数:11
相关论文
共 125 条
[1]   Synaptic computation [J].
Abbott, LF ;
Regehr, WG .
NATURE, 2004, 431 (7010) :796-803
[2]   The Future of Psychiatric Research: Genomes and Neural Circuits [J].
Akil, Huda ;
Brenner, Sydney ;
Kandel, Eric ;
Kendler, Kenneth S. ;
King, Mary-Claire ;
Scolnick, Edward ;
Watson, James D. ;
Zoghbi, Huda Y. .
SCIENCE, 2010, 327 (5973) :1580-1581
[3]  
[Anonymous], 1999, The genetical theory of natural selection: a complete variorum edition
[4]   Modeling madness in mice: One piece at a time [J].
Arguello, P. Alexander ;
Gogos, Joseph A. .
NEURON, 2006, 52 (01) :179-196
[5]   Cognition in Mouse Models of Schizophrenia Susceptibility Genes [J].
Arguello, P. Alexander ;
Gogos, Joseph A. .
SCHIZOPHRENIA BULLETIN, 2010, 36 (02) :289-300
[6]   Presenilin-Dependent Receptor Processing Is Required for Axon Guidance [J].
Bai, Ge ;
Chivatakarn, Onanong ;
Bonanomi, Dario ;
Lettieri, Karen ;
Franco, Laura ;
Xia, Caihong ;
Stein, Elke ;
Ma, Le ;
Lewcock, Joseph W. ;
Pfaff, Samuel L. .
CELL, 2011, 144 (01) :106-118
[7]   RETRACTED: Enhanced Polyubiquitination of Shank3 and NMDA Receptor in a Mouse Model of Autism (Retracted article. See vol. 152, pg. 367, 2013) [J].
Bangash, M. Ali ;
Park, Joo Min ;
Melnikova, Tatiana ;
Wang, Dehua ;
Jeon, Soo Kyeong ;
Lee, Deidre ;
Syeda, Sbaa ;
Kim, Juno ;
Kouser, Mehreen ;
Schwartz, Joshua ;
Cui, Yiyuan ;
Zhao, Xia ;
Speed, Haley E. ;
Kee, Sara E. ;
Tu, Jian Cheng ;
Hu, Jia-Hua ;
Petralia, Ronald S. ;
Linden, David J. ;
Powell, Craig M. ;
Savonenko, Alena ;
Xiao, Bo ;
Worley, Paul F. .
CELL, 2011, 145 (05) :758-772
[8]   Neuropsychological Abnormalities in Schizophrenia and Major Mood Disorders: Similarities and Differences [J].
Barch, Deanna M. .
CURRENT PSYCHIATRY REPORTS, 2009, 11 (04) :313-319
[9]   Clinically detectable copy number variations in a Canadian catchment population of schizophrenia [J].
Bassett, Anne S. ;
Costain, Gregory ;
Fung, Wai Lun Alan ;
Russell, Kathryn J. ;
Pierce, Laura ;
Kapadia, Ronak ;
Carter, Ronald F. ;
Chow, Eva W. C. ;
Forsythe, Pamela J. .
JOURNAL OF PSYCHIATRIC RESEARCH, 2010, 44 (15) :1005-1009
[10]   Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals [J].
Bijlsma, E. K. ;
Gijsbers, A. C. J. ;
Schuurs-Hoeijmakers, J. H. M. ;
van Haeringen, A. ;
van de Putte, D. E. Fransen ;
Anderlid, B. -M. ;
Lundin, J. ;
Lapunzina, P. ;
Perez Jurado, L. A. ;
Delle Chiaie, B. ;
Loeys, B. ;
Menten, B. ;
Oostra, A. ;
Verhelst, H. ;
Amor, D. J. ;
Bruno, D. L. ;
van Essen, A. J. ;
Hordijk, R. ;
Sikkema-Raddatz, B. ;
Verbruggen, K. T. ;
Jongmans, M. C. J. ;
Pfundt, R. ;
Reeser, H. M. ;
Breuning, M. H. ;
Ruivenkamp, C. A. L. .
EUROPEAN JOURNAL OF MEDICAL GENETICS, 2009, 52 (2-3) :77-87