原位凋亡Induction of apoptosis in the blue mussel Mytilus galloprovincialis原位凋亡Induction of apoptosis in the blue mussel Mytilus galloprovincialis.pdf
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原位凋亡Induction of apoptosis in the blue mussel Mytilus galloprovincialis原位凋亡Induction of apoptosis in the blue mussel Mytilus galloprovincialis
Aquatic Toxicology 55 (2001) 61–73 /locate/aquatox
Induction of apoptosis in the blue mussel Mytilus
galloproincialis by tri-n -butyltin chloride
a, a a b
Milena Micˇic´ *, Nevenka Bihari , Zeljka Labura , Werner E.G. Mu¨ller ,
Renato Batel a
a Center for Marine Research Roinj, Rudjer Bosˇkoic´ Institute, G. Paliage 5, 52210 Roinj, Croatia
b Institut fu¨r Physiologische Chemie, Abteilung Angewandte Molekularbiologie, Johannes Gutenberg Uniersita¨t, Duesbergweg 6,
D -55099 Mainz, Germany
Received 12 July 2000; received in revised form 24 January 2001; accepted 25 January 2001
Abstract
Induction of apoptosis by tri-n -butyltin (TBT) in gill tissue of the mussel Mytilus galloproincialis was investigated.
The terminal dUTP nick-end labeling technique (TUNEL) was used to detect cells displaying DNA fragmentation
within gill structures. Genomic DNA fragmentation was detected as characteristically ladder-like pattern of DNA
fragments induced by single injection of different doses of TBT (1–5 g/g) below the mantle, directly into the pallial
fluid, after 24 h of incubation. DNA degradation of higher order DNA structure, as well as reduced G0/G1 cell cycle
region (the sub-G1 region) was detectable after 1.5 h of TBT incubation. Presence of apoptotic cells in mussels’ gills
was indicated by the selective loss of G2/M cells concomitant with the appearance of cells wit
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