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A labile,Ca2+-dependent cytoskeleton in rhabdomeral microvilli of blowflies
Authors:Dr. A. D. Blest  Sally Stowe  Wendy Eddey
Affiliation:(1) Department of Neurobiology, Australian National University, Canberra, Australia;(2) Department of Neurobiology, Research School of Biological Science, Australian National University, P.O. Box 475, 2601 Canberra, A.C.T., Australia
Abstract:Summary Rhabdomeral microvilli of photoreceptors of the blowfly Lucilia are shown to contain a cytoskeleton. An axial filament (sim 6–11 nm) in each microvillus is inserted into a terminal cap distally, and into a plug filling the narrow neck of the microvillus proximally. In some states, the axial filament projects beyond the neck; within the microvillus it is surrounded by amorphous material. Together, they form an axial complex, which supports side-arms linking it to the plasma membrane. Conventional fixation for examination with the electron microscope destroys the cytoskeleton. To preserve it, retinae are pre-treated with a Ringer's solution buffered with 20 mM imidazole and containing, minimally, the following components: (i) a protease inhibitor, usually phenylmethylsulphonyl-fluoride (PMSF); (ii) either the Ca2+-chelator EGTA, or the calmodulin-blocking agent trifluoperazine (TFP); and (iii) a source of divalent cations to preserve the side-arms. When EGTA is used, Mg2+, Sr2+, Ba2+, Mn2+ and Co2+ are effective, Ba2+ giving the most satisfactory contrast, and Mg2+ and Co2+ the best preservation. It is inferred that the cytoskeletal complex includes at least one Ca2+-activated protease, and possibly calmodulin. Microvilli are bonded together by intermicrovillar bridges with a periodicity of 11–17nm. The cytoskeleton is destroyed by pretreatment with 1 mM dithiothreitol (DTT), possibly by the activation of a thiol protease. It does not survive osmication unless treated with low molecular weight tannic acid (LMWT). The evidence does not discriminate between actin and intermediate filaments as the basis of the cytoskeleton. Attention is drawn to similarities and differences between the rhabdomeral cytoskeleton and that of vertebrate intestinal brush-borders. The extreme lability of the rhabdomeral cytoskeleton to conventional methods of fixation is attributed in part to the Ca2+ fluxes experienced by invertebrate photoreceptors, and in part to the effects of osmication.The authors thank Dr. Lindsay Barton-Brown and Tom Van Gerwen for supplying flies from CSIRO cultures: Smith Kline and French Laboratories Ltd., French's Forest, N.S.W. for a generous gift of trifluoperazine, and Mallinckrodt, Inc., St. Louis, Missouri, USA, for a gift of low molecular weight tannic acid. Many colleagues, especially Richard Payne, Steve Shaw and Gert De Couet helped by discussing the results. George Weston and the staff of the Electron Microscope Unit provided support and advice. Sandy Smith prepared Table 1
Keywords:Rhabdomeral microvilli  Cytoskeleton  Ca2+-Protease  Actin  Intermediate filaments  Blowfly
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