CELLULAR ALTERATIONS IN COLLEMBOLAN MIDGUT CELLS AS A MARKER OF HEAVY-METAL EXPOSURE - ULTRASTRUCTURE AND INTRACELLULAR METAL DISTRIBUTION

Citation
M. Pawert et al., CELLULAR ALTERATIONS IN COLLEMBOLAN MIDGUT CELLS AS A MARKER OF HEAVY-METAL EXPOSURE - ULTRASTRUCTURE AND INTRACELLULAR METAL DISTRIBUTION, Science of the total environment, 181(3), 1996, pp. 187-200
Citations number
60
Categorie Soggetti
Environmental Sciences
ISSN journal
00489697
Volume
181
Issue
3
Year of publication
1996
Pages
187 - 200
Database
ISI
SICI code
0048-9697(1996)181:3<187:CAICMC>2.0.ZU;2-Q
Abstract
The ultrastructure of the midgut epithelial cells of Tetrodontophora b ielanensis (Collembola) fed either with lead-, cadmium- or zinc-enrich ed food or kept under control conditions was compared by transmission electron microscopy (TEM), Atomic absorption spectrophotometry (AAS) s howed accumulation of these three metals in the body tissues of the co llembolans, Intracellular localization of zinc in the midgut epithelia l cells was investigated by electron spectroscopic imaging (ESI) and e lectron energy loss spectroscopy (EELS). The presence of lead in the m idgut tissue was shown by laser microprobe mass spectrometry (LAMMS). Under heavy metal conditions, the midgut cells showed different ultras tructural alterations, the degree of which was found to be dose-depend ent. Independent of the type of the metal in the food, the endoplasmic reticulum appeared fenestrated or vesiculated, and often large vacuol es, which were shown to be ER-derived, occurred throughout the cells, Also the mitochondrial membranes were affected by heavy metal stress, In epithelial cells of individuals exposed to either lead or cadmium, an increase of myelin-like structures could be observed. In the case o f exposure to zinc in the highest applied concentration, the cytoplasm showed condensation and portions of the microvillous border appeared destroyed, Additionally, an increase of mineral congregations (type-A spherites) could be observed under heavy metal influence. Intracellula rly stored zinc could be localised at highly affected mitochondrial me mbranes, in the microvillous border, and in the heterochromatin.