E. Bollo et al., TRIPHENYLTIN ACETATE TOXICITY - A BIOCHEMICAL AND ULTRASTRUCTURAL-STUDY ON MOUSE THYMOCYTES, Human & experimental toxicology, 15(3), 1996, pp. 219-225
1 Triphenyltin acetate (TPTA) has been shown to exert in vivo a select
ive toxic effect on the immune system. To assess in vitro possible alt
erations induced by TPTA exposure, primary cultures of mouse thymocyte
s were incubated up to 24 h with graded amounts (1 - 12 mu M) of the o
rganotin. 2 The cytotoxic activity has been evaluated with the MTT col
orimetric assay, the neutral red (NR) assay and the lactic dehydrogena
se (LDH) cellular release. Cell pellets were fixed with 2.5% glutarald
ehyde, resin-embedded and ultrathin sections were observed through tra
nsmission electron microscopy. 3 After 2 h of incubation, dose-depende
nt increases of cytotoxicity were observed in thymocytes submitted to
MTT and NR tests (up to 41.43% and 18.9%, respectively), while 22 h la
ter this overt effect on cell viability was noticed merely in cells ex
posed to 12 mu M TPTA. Dose-dependent increases of LDH leakage in the
culture medium were observed all throughout the study. 4 Morphological
investigations revealed features (chromatin condensation, cell membra
nes fragmentation and formation of membrane bound apoptotic bodies) su
ggestive of apoptosis. 5 This study indicates that TPTA is cytotoxic t
o mouse thymocytes: morphologically, the rising of apoptosis is likely
to be recognized, as previously reported in different in vitro studie
s with other immunosuppressive agents as dioxin and corticosteroids.