Differential subcellular localization of zinc in the rat retina

被引:42
作者
Akagi, T
Kaneda, M [1 ]
Ishii, K
Hashikawa, T
机构
[1] Keio Univ, Sch Med, Dept Physiol, Tokyo 1608582, Japan
[2] RIKEN, Brain Sci Inst, Lab Neural Architecture, Wako, Saitama 35101, Japan
关键词
synaptic terminal; Golgi apparatus; silver amplification; pigment epithelial cell; electron microscopy;
D O I
10.1177/002215540104900109
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In the retina, zinc is believed to be a modulator of synaptic transmission and a constituent: of metalloenzymes. To determine whether the intracellular localization of zinc correlates with function, we examined the localization of endogenous zinc in the rat retina using the silver amplification method. By light microscopy, reaction products were detected in the pigment epithelial cells (PE), the inner segment of photoreceptors (IS), the outer nuclear layer (ONL) and the inner nuclear layer (INL), the outer plexiform layer (OPL) and the inner plexiform layer (IPL), and the ganglion cell layer (CC). The heaviest accumulation of precipitate was observed in PE and IS, whereas only a little precipitate was found in GC. When the intracellular zinc was chelated with diethyldithiocarbamate, a small amount of precipitate was observed only in ONL. By electron microscopy, zinc was associated with three compartments. In OPL and IPL, zinc was associated with neural processes, while in PE, IS, INL and GC it was associated with the Golgi apparatus. In ONL, zinc was associated with the nucleus. Zinc in the neural processes is believed to act as a modulator of synaptic transmission, and zinc associated with the Golgi apparatus is assumed to catalyze metalloenzyme reactions.
引用
收藏
页码:87 / 96
页数:10
相关论文
共 43 条
[1]  
Akagi T., 1999, Society for Neuroscience Abstracts, V25, P135
[2]   SELECTIVE RELEASE OF ENDOGENOUS ZINC FROM THE HIPPOCAMPAL MOSSY FIBERS INSITU [J].
ANIKSZTEJN, L ;
CHARTON, G ;
BENARI, Y .
BRAIN RESEARCH, 1987, 404 (1-2) :58-64
[3]   RELEASE OF ENDOGENOUS ZN-2+ FROM BRAIN-TISSUE DURING ACTIVITY [J].
ASSAF, SY ;
CHUNG, SH .
NATURE, 1984, 308 (5961) :734-736
[4]   RECEPTIVE FIELDS OF CONES IN RETINA OF TURTLE [J].
BAYLOR, DA ;
FUORTES, MGF ;
OBRYAN, PM .
JOURNAL OF PHYSIOLOGY-LONDON, 1971, 214 (02) :265-&
[5]   ZINC PROTEINS - ENZYMES, STORAGE PROTEINS, TRANSCRIPTION FACTORS, AND REPLICATION PROTEINS [J].
COLEMAN, JE .
ANNUAL REVIEW OF BIOCHEMISTRY, 1992, 61 :897-946
[6]   AUTOMETALLOGRAPHY - TISSUE METALS DEMONSTRATED BY A SILVER ENHANCEMENT KIT [J].
DANSCHER, G ;
NORGAARD, JOR ;
BAATRUP, E .
HISTOCHEMISTRY, 1987, 86 (05) :465-469
[8]   The autometallographic zinc-sulphide method. A new approach involving in vivo creation of nanometer-sized zinc sulphide crystal lattices in zinc-enriched synaptic and secretory vesicles [J].
Danscher, G .
HISTOCHEMICAL JOURNAL, 1996, 28 (05) :361-373
[9]   A simplified procedure for the physical development of the sulphide silver method to reveal synaptic zinc in combination with immunocytochemistry at light and electron microscopy [J].
De Biasi, S ;
Bendotti, C .
JOURNAL OF NEUROSCIENCE METHODS, 1998, 79 (01) :87-96
[10]   ZINC DOWN-MODULATES THE GABA(C) RECEPTOR CURRENT IN CONE HORIZONTAL CELLS ACUTELY ISOLATED FROM THE CATFISH RETINA [J].
DONG, CJ ;
WERBLIN, FS .
JOURNAL OF NEUROPHYSIOLOGY, 1995, 73 (02) :916-919