Expression of vesicular glutamate transporter 1 in the mouse retina reveals temporal ordering in development of rod vs. cone and ON vs. OFF circuits

被引:157
作者
Sherry, DM [1 ]
Wang, MM [1 ]
Bates, J [1 ]
Frishman, LJ [1 ]
机构
[1] Univ Houston, Coll Optometry, Houston, TX 77204 USA
关键词
VGLUT; glutamate; ribbon synapses; synaptogenesis; bipolar cells; photoreceptors; development; retina;
D O I
10.1002/cne.10838
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Glutamatergic transmission is crucial to the segregation of ON and OFF pathways in the developing retina. The temporal sequence of maturation of vesicular glutamatergic transmission in rod and cone photoreceptor and ON and OFF bipolar cell terminals is currently unknown. Vesicular glutamate transporters (VGLUTs) that load glutamate into synaptic vesicles are necessary for vesicular glutamatergic transmission. To understand better the formation and maturation of glutamatergic transmission in the rod vs. cone and ON vs. OFF pathways of the retina, we examined the developmental expression of VGLUT1 and VGLUT2 immunocytochemically in the mouse retina. Photoreceptor and bipolar cell terminals showed only VGLUT1-immunoreactivity (-IR); no VGLUT2-IR was present in any synapses of the developing or adult retina. VGLUT1-IR was first detected in cone photoreceptor terminals at postnatal day 2 (P2), several days before initiation of ribbon synapse formation at P4-P5. Rod terminals showed VGLUT1-lR by P8, when they invade the outer plexiform layer (OPL) and initiate synaptogenesis. Developing OFF bipolar cell terminals showed VGLUT1-IR around P8, 2-3 days after bipolar terminals were first identified in the inner plexiforin layer (IPL) by labeling for the photoreceptor and bipolar cell terminal marker, synaptic vesicle protein 2B. Although terminals of ON bipolar cells were present in the IPL by P6-P8, most did not show VGLUT1-IR until P8-P10 and increased dramatically from P12. These data suggest a hierarchical development of glutamatergic transmission in which cone circuits form prior to rod circuits in both the OPL and IPL, and OFF circuits form prior to ON circuits in the IPL. J. Comp. Neurol. 465:480-498, 2003. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:480 / 498
页数:19
相关论文
共 64 条
[1]   Assembly of presynaptic active zones from cytoplasmic transport packets [J].
Ahmari, SE ;
Buchanan, J ;
Smith, SJ .
NATURE NEUROSCIENCE, 2000, 3 (05) :445-451
[2]   Molecular cloning of a novel brain-type Na+-dependent inorganic phosphate cotransporter [J].
Aihara, Y ;
Mashima, H ;
Onda, H ;
Hisano, S ;
Kasuya, H ;
Hori, T ;
Yamada, S ;
Tomura, H ;
Yamada, Y ;
Inoue, I ;
Kojima, I ;
Takeda, J .
JOURNAL OF NEUROCHEMISTRY, 2000, 74 (06) :2622-2625
[3]   DIFFERENTIAL EXPRESSION OF SNAP-25 PROTEIN ISOFORMS DURING DIVERGENT VESICLE FUSION EVENTS OF NEURAL DEVELOPMENT [J].
BARK, IC ;
HAHN, KM ;
RYABININ, AE ;
WILSON, MC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (05) :1510-1514
[4]  
Bellocchio EE, 1998, J NEUROSCI, V18, P8648
[5]  
Bergmann M, 2000, J COMP NEUROL, V418, P361
[6]  
BLANKS JC, 1984, INVEST OPHTH VIS SCI, V25, P546
[7]   SYNAPTOGENESIS IN PHOTORECEPTOR TERMINAL OF MOUSE RETINA [J].
BLANKS, JC ;
ADINOLFI, AM ;
LOLLEY, RN .
JOURNAL OF COMPARATIVE NEUROLOGY, 1974, 156 (01) :81-93
[8]   STRATIFICATION OF ON AND OFF GANGLION-CELL DENDRITES DEPENDS ON GLUTAMATE-MEDIATED AFFERENT ACTIVITY IN THE DEVELOPING RETINA [J].
BODNARENKO, SR ;
CHALUPA, LM .
NATURE, 1993, 364 (6433) :144-146
[9]  
BODNARENKO SR, 1995, J NEUROSCI, V15, P7037
[10]  
BUCKLEY K, 1985, J CELL BIOL, V100, P1284, DOI 10.1083/jcb.100.4.1284