E. Pyza et Ia. Meinertzhagen, CIRCADIAN-RHYTHMS IN SCREENING PIGMENT AND INVAGINATING ORGANELLES INPHOTORECEPTOR TERMINALS OF THE HOUSEFLYS FIRST OPTIC NEUROPIL, Journal of neurobiology, 32(5), 1997, pp. 517-529
Screening pigment granules occur in the synaptic terminals of photorec
eptors in the fly's (Musca domestica, L.) compound eye. The granules r
esemble ommochrome granules in the overlying photoreceptor cell body.
There are also two types of invagination into receptor terminals: capi
tate projections (from glial cells) and invaginations from neighboring
receptor terminals. The number of profiles of these organelles in the
first optic neuropile, the lamina, have been counted using single-sec
tion quantitative electron microscopic methods. Pigment granules are c
oncentrated proximally in the terminal, toward the brain. The numbers
change, increasing during the night (Ih after lights off) up to values
more than twice the number Ih after lights on, apparently by longitud
inal migration of granules from the cell body into the terminal. Flies
entrained to day/night conditions and then held under constant darkne
ss continue to exhibit changes in the numbers of profiles. Even though
overall there were 80-90% fewer granule profiles than under day/night
conditions, the numbers attained a peak many times higher at the end
of the subjective day. Thus, the changes are endogenous, showing circa
dian rhythmicity. Although their significance is unknown, these change
s parallel previously described circadian rhythms in the receptor term
inals and their lamina monopolar-cell targets. The invaginations from
receptor terminals were more numerous under day/night conditions than
under constant darkness, and cycled in constant darkness, peaking at t
he end of subjective night. Capitate projections, by contrast, failed
to change significantly under the experimental conditions analyzed, a
lack of responsiveness they share with photoreceptor tetrad synapses.
(C) 1997 John Wiley & Sons, Inc.