Detection of pathological zinc accumulation in neurons: Methods for autopsy, biopsy, and cultured tissue

被引:30
作者
Suh, SW
Listiack, K
Bell, B
Chen, J
Motamedi, M
Silva, D
Danscher, G
Whetsell, W
Thompson, R
Frederickson, C
机构
[1] Neurobiotex Inc, Galveston, TX 77550 USA
[2] Univ Texas, Med Branch, Ctr Biomed Engn, Galveston, TX 77550 USA
[3] Microfab Technol Inc, Lab Zinc Neurobiol, Plano, TX USA
[4] Univ Aarhus, Inst Neurobiol, Aarhus, Denmark
[5] Vanderbilt Univ, Sch Med, Dept Pathol, Nashville, TN 37212 USA
[6] Univ Maryland, Dept Chem, Baltimore, MD 21201 USA
关键词
zinc; neuronal injury; perikarya; dendrites; staining;
D O I
10.1177/002215549904700715
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It has been repeatedly shown that synaptically released zinc contributes to excitotoxic neuronal injury in ischemia, epilepsy, and mechanical head trauma. Such zinc-induced injury leaves an unmistakable "footprint" in the injured neurons, allowing an easy and unambiguous postmortem diagnosis. This footprint is the presence of weakly bound, histochemically reactive zinc in the cytoplasm of the perikaryon and proximal dendrites. Such staining appears to be a necessary and sufficient marker for zinc-induced neuronal injury. Here we show how to prepare and stain tissue from biopsy, autopsy, or experimental animal sources for maximal contrast and visibility of zinc-injured neurons.
引用
收藏
页码:969 / 972
页数:4
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