The Striosome and Matrix Compartments of the Striatum: A Path through the Labyrinth from Neurochemistry toward Function

被引:115
作者
Brimblecombe, Katherine R. [1 ]
Cragg, Stephanie J. [1 ,2 ]
机构
[1] Univ Oxford, Dept Physiol Anat & Genet, Sherrington Bldg, Oxford OX1 3PT, England
[2] Univ Oxford, Oxford Parkinsons Dis Ctr, Oxford OX1 3PT, England
基金
英国医学研究理事会;
关键词
Striosome; matrix; striatum; basal ganglia; dopamine; substance P; acetylcholine; cholinergic interneurons; transgenic tools; MU-OPIOID RECEPTOR; SUBSTANCE-P; DOPAMINE RELEASE; BASAL GANGLIA; CHOLINERGIC INTERNEURONS; EXTRASTRIOSOMAL MATRIX; TYROSINE-HYDROXYLASE; NUCLEUS-ACCUMBENS; INTRINSIC NEURONS; CAUDATE-NUCLEUS;
D O I
10.1021/acschemneuro.6b00333
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The striatum is a heterogeneous structure with a diverse range of neuron types and neuromodulators. Three decades of anatomical and biochemical studies have established that the neurochemical organization of striatum is not uniformly heterogeneous, but rather, can be differentiated into neurochemically discrete compartments known as striosomes (also known as patches) and matrix. These compartments are well understood to differ in their expression of neurochemical markers, with some differences in afferent and efferent connectivity and have also been suggested to have different involvement in a range of neurological diseases. However, the functional outcomes of striosome matrix organization are poorly understood. Now, recent findings and new experimental tools are beginning to reveal that the distinctions between striosomes and matrix have distinct consequences for striatal synapse function. Here, we review recent findings that suggest there can be distinct regulation of neural function in striosome versus matrix compartments, particularly compartment-specific neurochemical interactions. We highlight that new transgenic and viral tools are becoming available that should now accelerate the pace of advances in understanding of these long-mysterious striatal compartments.
引用
收藏
页码:235 / 242
页数:8
相关论文
共 92 条
[1]   Shifting responsibly: the importance of striatal modularity to reinforcement learning in uncertain environments [J].
Amemori, Ken-ichi ;
Gibb, Leif G. ;
Graybiel, Ann M. .
FRONTIERS IN HUMAN NEUROSCIENCE, 2011, 5 :1
[2]   The AAV Vector Toolkit: Poised at the Clinical Crossroads [J].
Asokan, Aravind ;
Schaffer, David V. ;
Samulski, R. Jude .
MOLECULAR THERAPY, 2012, 20 (04) :699-708
[3]   Enkephalin Disinhibits Mu Opioid Receptor-Rich Striatal Patches via Delta Opioid Receptors [J].
Banghart, Matthew Ryan ;
Neufeld, Shay Quentin ;
Wong, Nicole Christine ;
Sabatini, Bernardo Luis .
NEURON, 2015, 88 (06) :1227-1239
[4]  
Beil J., 2012, J BIOMED BIOTECHNOL, V2012, P1
[5]   Morphological features, distribution and compartmental organization of the nicotinamide adenine dinucleotide phosphate reduced-diaphorase interneurons in the human striatum [J].
Bernácer, J ;
Prensa, L ;
Giménez-Amaya, JM .
JOURNAL OF COMPARATIVE NEUROLOGY, 2005, 489 (03) :311-327
[6]   Cholinergic Interneurons Are Differentially Distributed in the Human Striatum [J].
Bernacer, Javier ;
Prensa, Lucia ;
Manuel Gimenez-Amaya, Jose .
PLOS ONE, 2007, 2 (11)
[7]   Distribution of GABAergic Interneurons and Dopaminergic Cells in the Functional Territories of the Human Striatum [J].
Bernacer, Javier ;
Prensa, Lucia ;
Manuel Gimenez-Amaya, Jose .
PLOS ONE, 2012, 7 (01)
[8]   THE C-TERMINAL FRAGMENT OF SUBSTANCE-P ENHANCES DOPAMINE RELEASE IN NUCLEUS-ACCUMBENS BUT NOT IN NEOSTRIATUM IN FREELY MOVING RATS [J].
BOIX, F ;
HUSTON, JP ;
SCHWARTING, RKW .
BRAIN RESEARCH, 1992, 592 (1-2) :181-186
[9]   Synaptic organisation of the basal ganglia [J].
Bolam, JP ;
Hanley, JJ ;
Booth, PAC ;
Bevan, MD .
JOURNAL OF ANATOMY, 2000, 196 :527-542
[10]  
BOLAM JP, 1988, EXP BRAIN RES, V70, P361