Autometallography (AMG) - Silver enhancement of quantum dots resulting from (1) metabolism of toxic metals in animals and humans, (2) in vivo, in vitro and immersion created zinc-sulphur/zinc-selenium nanocrystals, (3) metal ions liberated from metal implants and particles

被引:94
作者
Danscher, Gorm [1 ]
Stoltenberg, Meredin [1 ]
机构
[1] Univ Aarhus, Inst Anat, Dept Neurobiol, DK-8000 Aarhus, Denmark
关键词
autometallography (AMG); silver; gold; zinc; nanocrystals; quantum dots; bismuth; mercury; histochemistry;
D O I
10.1016/j.proghi.2006.06.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autometallographic (AMG) silver enhancement is a potent histochemical tool for tracing a variety of metal containing nanocrystals, e.g. pure gold and silver nanoclusters and quantum dots of silver, mercury, bismuth or zinc, with sulphur and/or selenium. These nanocrystals can be created in many different ways, e.g. (1) by manufacturing colloidal gold or silver particles, (2) by treating an organism in vivo with sulphide or selenide ions, (3) as the result of a metabolic decomposition of bismuth-, mercury- or silver-containing macromolecules in cell organelles, or (4) as the end product of histochemical processing of tissue sections. Such nano-sized AMG nanocrystals can then be silver-amplified several times of magnitude by being exposed to an AMG developer, i.e. a normal photographic developer enriched with silver ions. The present monograph attempts to provide a review of the autometallographic silver amplification techniques known today and their use in biology. After achieving a stronghold in histochemistry by Timm's introduction of the "silver-sulphide staining" in 1958, the AMG technique has evolved and expanded into several different areas of research, including immunocytochemistry, tracing of enzymes at LM and EM levels, blot staining, retrograde axonal tracing of zinc-enriched (ZEN) neurons, counterstaining of semithin sections, enhancement of histochemical reaction products, marking of phagocytotic cells, staining of myelin, tracing of gold ions released from gold implants, and visualization of capillaries. General technical comments, protocols for the current AMG methods and a summary of the most significant scientific results obtained by this wide variety of AMG histochemical approaches are included in the present article. (c) 2006 Elsevier GmbH. All rights reserved.
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收藏
页码:57 / 139
页数:83
相关论文
共 255 条
[1]   ARGYRIA - TISSUE DEPOSITION OF SILVER AS SELENIDE [J].
AASETH, J ;
OLSEN, A ;
HALSE, J ;
HOVIG, T .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1981, 41 (03) :247-251
[2]  
ARENHOLTBINDSLEV D, 1989, ATLA-ALTERN LAB ANIM, V16, P253
[3]   INORGANIC MERCURY IS TRANSPORTED FROM MUSCULAR NERVE-TERMINALS TO SPINAL AND BRAIN-STEM MOTONEURONS [J].
ARVIDSON, B .
MUSCLE & NERVE, 1992, 15 (10) :1089-1094
[4]   CYTOCHEMICAL DEMONSTRATION OF MERCURY DEPOSITS IN TROUT LIVER AND KIDNEY FOLLOWING METHYL MERCURY INTOXICATION - DIFFERENTIATION OF 2 MERCURY POOLS BY SELENIUM [J].
BAATRUP, E ;
DANSCHER, G .
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 1987, 14 (02) :129-141
[6]   Zinc co-localizes with GABA and glycine in synapses in the lamprey spinal cord [J].
Birinyi, A ;
Parker, D ;
Antal, M ;
Shupliakov, O .
JOURNAL OF COMPARATIVE NEUROLOGY, 2001, 433 (02) :208-221
[7]   AMALGAM ASSOCIATED MERCURY ACCUMULATIONS IN NORMAL ORAL-MUCOSA, ORAL MUCOSAL LESIONS OF LICHEN-PLANUS AND CONTACT LESIONS ASSOCIATED WITH AMALGAM [J].
BOLEWSKA, J ;
HOLMSTRUP, P ;
MOLLERMADSEN, B ;
KENRAD, B ;
DANSCHER, G .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1990, 19 (01) :39-42
[8]   THALLIUM ACTIVATION OF (NA+-K+)-ACTIVATED ATPASE OF RABBIT KIDNEY [J].
BRITTEN, JS ;
BLANK, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1968, 159 (01) :160-&
[9]   An improved method for visualizing the cell bodies of zincergic neurons [J].
Brown, CE ;
Dyck, RH .
JOURNAL OF NEUROSCIENCE METHODS, 2003, 129 (01) :41-47
[10]   HISTOCHEMICAL EVIDENCE FOR LYSOSOMAL UPTAKE OF LEAD IN TISSUE CULTURED FIBROBLASTS [J].
BRUNK, U ;
BRUN, A .
HISTOCHEMIE, 1972, 29 (02) :140-&