Metallothioneins (MTs) are sulfhydryl-rich proteins binding essential and n
on-essential heavy metals. MTs display in vitro oxyradical scavenging capac
ity, suggesting that they may specifically neutralize hydroxyl radicals, Ye
t, this is probably an oversimplified view, as MTs represent a superfamily
of widely differentiated metalloproteins, MT antioxidant properties mainly
derive from sulfhydryl nucleophilicity, but also from metal complexation. B
inding of transition metals displaying Fenton reactivity (Fe, Cu) can reduc
e oxidative stress, whereas their release exacerbates it. In vertebrates, M
T gene promoters contain metal (MRE) and glucocorticoid response elements (
GRE), Sp and AP sequences, but also antioxidant response elements (ARE). MT
neosynthesis is induced by heavy metals, cytokines, hormones, but also by
different oxidants and prooxidants, Accordingly, MT overexpression increase
s the resistance of tissues and cells to oxidative stress. As for invertebr
ates, data from the mussel show that MT can actually protect against oxidat
ive stress, but is poorly inducible by oxidants, In yeast there is a Cu(I)-
MT that in contrast to mammal Cu-MT exhibits antioxidant activity, possibly
due to differences in metal binding domains. Finally, as the relevance of
redox processes in cell signaling is becoming more and more evident, a sear
ch for MT effects on redox signaling could represent a turning point in the
understanding of the functional role of these protein.