M. Mcnulty et al., Evidence that a copper-metallothionein complex is responsible for fluorescence in acid-secreting cells of the Drosophila stomach, CELL TIS RE, 304(3), 2001, pp. 383-389
Copper cells were originally identified in Drosophila midgut epithelium by
their striking orange fluorescence in copper-fed larvae. Here, we examined
copper cell fluorescence in light of the previous observations that (1) a s
imilar fluorescent signal in yeast is produced by a complex between copper
and metallothionein, and (2) metallothionein is expressed constitutively in
the copper cell region and inducibly in other regions of the Drosophila mi
dgut. Pulse-feeding experiments with 1 mM CuCl2 revealed that fluorescence
appeared rapidly in copper cells (<5 min) and slowly in other cells of the
midgut (days), suggesting a constitutive cofactor in the former and an indu
cible cofactor in the latter. Fluorescence was also detected in Drosophila
S2 tissue culture cells after induction of metallothionein synthesis by add
ition of CuCl2 to the growth medium. Thus, fluorescence coincided spatially
and temporally with the expression of metallothionein. Fluorescence was al
so linked to the acid-secreting activity of copper cells. Fluorescence was
not observed when acid secretion was inhibited by a mutation in the a spect
rin gene and acidification was blocked in copper-fed wild-type larvae. Howe
ver, acidification was restored after a 1-day chase period in which the flu
orescent signal became sequestered within a vesicular compartment. We there
fore conclude that copper cell fluorescence is most probably attributable t
o a cytoplasmic copper-metallothionein complex, suggesting an unanticipated
role for metallothionein in acid-secreting cells.