A PHOSPHOLIPASE INHIBITOR, MANOALIDE, AND A G-PROTEIN ACTIVATOR, MAS-7, BOTH AFFECT THE TURNOVER OF PHOTOTRANSDUCTIVE MEMBRANES BY CRAB RETINAS IN DARKNESS - WITH A MODEL FOR THE REGULATION OF RHABDOMERAL MEMBRANE TURNOVER
Ad. Blest et S. Stowe, A PHOSPHOLIPASE INHIBITOR, MANOALIDE, AND A G-PROTEIN ACTIVATOR, MAS-7, BOTH AFFECT THE TURNOVER OF PHOTOTRANSDUCTIVE MEMBRANES BY CRAB RETINAS IN DARKNESS - WITH A MODEL FOR THE REGULATION OF RHABDOMERAL MEMBRANE TURNOVER, Journal of comparative physiology. A, Sensory, neural, and behavioral physiology, 180(4), 1997, pp. 347-355
(1) In vitro retinas of a crab, Leptograpsus, were treated with a phos
pholipase inhibitor, manoalide, or a G-protein activator, Mas-7. Both
drugs address early stages of the phototransduction cascade. (2) Manoa
lide inhibited the light-dependent reduction of rhabdoms during the 'd
ay' phase of the light cycle, but did not induce rhabdom overgrowth. F
ollowing a period of darkness manoalide failed to affect the diminutio
n of illuminated rhabdoms. (3) The diminution of rhabdoms that follows
photoreceptor depolarisation induced by 100 mmol . l(-1) K+ in darkne
ss was not affected by 2 mu mol . l(-1) manoalide. (4) When retinas in
the 'night' phase were treated with Mas-7 in darkness, rhabdom diamet
ers were augmented, concurrently with endocytosis of photoreceptor pla
sma membranes. (5) The results of combining manoalide and Mas-7 with a
ctinomycin D, U-57908 or okadaic acid, drugs used in previous studies
to manipulate steps notionally lower in the transduction cascade, lead
to a hypothetical model for the regulation of phototransductive membr
ane turnover by arthropods.