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Accessibility of colloidal gold and horseradish peroxidase to cytosolic spaces in Limulus ventral photoreceptors

Published online by Cambridge University Press:  02 June 2009

L. J. Rubin*
Affiliation:
Department of Ophthalmology, WashingtonUniversity School of Medicine, St. Louis
M. Womble
Affiliation:
Department of Cellular and Structural Biology, University of Colorado School of Medicine, Denver
J. E. Brown
Affiliation:
Department of Ophthalmology, WashingtonUniversity School of Medicine, St. Louis
T. E. Finger
Affiliation:
Department of Cellular and Structural Biology, University of Colorado School of Medicine, Denver
*
Correspondence to: Leona J. Rubin, Department of Pharmacology, 8103, Washington University School of Medicine, 660 S. Euclid Avenue, St. Louis, MO 63110, USA.

Abstract

Physiological studies of intracellular messengers frequently employ intracellular injections of large molecules that either monitor or modulate the metabolism of the messenger cascade. Injected molecules have unknown mobility in the cytosol and unknown accessibility to various cytosolic compartments, including those postulated to be traversed by intracellular messenger molecules. In order to determine whether injected molecules have access to the confined spaces through which messenger molecules must diffuse, we injected 5-nm colloidal gold or horseradish peroxidase, or both, into Limulus ventral photoreceptors. Injections were made by applying pressure pulses to the back of an intracellular micropipette that also monitored membrane voltage. The tissue was fixed at varying times after injection and processed for electron microscopy by conventional techniques. Cells fixed 1–3 min after injection contained HRP reaction product only in the cell body. HRP reaction product was found at varying distances down axons in direct relation to the interval between injection and fixation. Colloidal gold particles were found throughout the cell body but not in axons of tissue fixed 1–3 min after injection. Both HRP reaction product and 5-nm colloidal gold particles were observed within the microvillar projections of internal and external rhabdomere, as well as within the extracisternal spaces of endoplasmic reticulum. We conclude that large molecules injected from an intracellular micropipette into an arbitrary locus of ventral photoreceptor cells have access to all of the presumed sites of the phototransduction cascade.

Type
Research Articles
Copyright
Copyright © Cambridge University Press 1989

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References

Battelle, B.A.Evans, J.A. & Chamberlain, S.C. (1982). Efferent fibers to Limulus eyes synthesize and release octopamine. Science 216, 12501252.CrossRefGoogle Scholar
Brown, J.E. & Blinks, J.R. (1974). Changes in intracellular free calcium during illumination of invertebrate photoreceptors. Detection with aequorin. Journal of General Physiology 64, 643665.CrossRefGoogle ScholarPubMed
Calman, B.C. & Chamberlain, S.C. (1982). Distinct lobes of Limulus ventral photoreceptors. II. Structure and ultrastructure. Journal of General Physiology 80, 839862.CrossRefGoogle ScholarPubMed
Clark, A.W., Millecchia, R. & Mauro, A. (1969). The ventral photoreceptor cells of Limulus. I. The microanatomy. Journal of General Physiology 54, 289309.CrossRefGoogle ScholarPubMed
Corson, D.W. & Fein, A. (1983). Quantitative pressure injections of picoliter volumes into Limulus ventral photoreceptors. Biophysical Journal 44, 299344.CrossRefGoogle ScholarPubMed
Courtoy, P.J., Picton, D.H. & Farquhar, M.G. (1983). Resolution and limitations of the immunoperoxidase procedure in the localization of extracellular matrix antigens. Journal of Histochemistry and Cytochemistry 31, 945951.CrossRefGoogle ScholarPubMed
Fahrenbach, W.H. (1969). The morphology of the eyes of Limulus. II. Ommatidia of the compound eye. Zeitschrift für Zellforschung und Mikroskopische Anatomic 93, 451483.CrossRefGoogle ScholarPubMed
Fahrenbach, W.H. (1985). Anatomical circuitry of lateral inhibition in the eye of the horseshoe crab, Limulus polyphemus. Proceedings of the Royal Society of London B 255, 219249.Google Scholar
Feldherr, C.M., Kallenbach, E. & Schultz, N. (1984). Movement of a karyophilic protein through the nuclear pores of oocytes. Journal of Cell Biology 99, 22162222.CrossRefGoogle ScholarPubMed
Hanker, J.S., Yates, P.E., Metz, C.B. & Rustioni, A. (1977). A new specific, sensitive, and noncarcinogenic reagent for the demonstration of horseradish peroxidase. Histochemical Journal 9, 789792.CrossRefGoogle ScholarPubMed
Lisman, J.E. & Brown, J.E. (1975). Effects of intracellular injection of calcium buffers on light adaptation in Limulus ventral photoreceptors. Journal of General Physiology 66, 489506.CrossRefGoogle ScholarPubMed
Lisman, J.E. & Strong, A. (1979). The initiation of excitation and light adaptation in Limulus ventral photoreceptors. Journal of General Physiology 73, 219243.CrossRefGoogle ScholarPubMed
Mazariego, M.R. & Hand, A.R. (1985). Horseradish peroxidase: factors affecting its distribution after retrograde infusion into rat parotid gland. Journal of Histochemistry 33 942950.Google Scholar
Messing, A., Stieber, A. & Gonatas, N.K. (1985). Resolution of diaminobenzidine for detection of horseradish peroxidase on surfaces of cultured cells. Journal of Histochemistry and Cytochemistry 33, 837839.CrossRefGoogle ScholarPubMed
Millecchia, R. & Mauro, A. (1969 a). The ventral photoreceptor cells of Limulus. II. Basic photoresponse. Journal of General Physiology 54, 310330.CrossRefGoogle ScholarPubMed
Millecchia, R. & Mauro, A. (1969 b). The ventral photoreceptor cells of Limulus. III. A voltage-clamp study. Journal of General Physiology 54, 331351.CrossRefGoogle Scholar
Payne, R., Corson, D.W., Fein, A. & Berridge, M.J. (1986). Excitation and adaptation of Limulus ventral photoreceptors by inositol 1,4,5 trisphosphate result from a rise in intracellular calcium. Journal of General Physiology 88, 127142.CrossRefGoogle ScholarPubMed
Rubin, L.J., Brown, J.E. & Poznanski, M. (1986). Injection of phospholipase C into Limulus ventral photoreceptors. Biophysical Journal 49, 30a.Google Scholar
Rubin, L.J. & Brown, J.E. (1988). Intracellular [ATP] in Limulus ventral photoreceptors: concentration is not correlated with responsiveness or rate of discrete events in darkness. American Journal of Physiology 254, C27C36.CrossRefGoogle Scholar
Stern, J., Chinn, K., Bacigalupo, J & Lisman, J. (1982). Distinct lobes of Limulus ventral photoreceptors. I. Functional and anatomical properties of lobes revealed by removal of glial cells. Journal of General Physiology 80, 825837.CrossRefGoogle ScholarPubMed
Walz, B. (1982). Ca2+-sequestering smooth endoplasmic reticulum in an invertebrate photoreceptor. I. Intracellular topography as revealed by CsFeCN staining and in situ Ca accumulation. Journal of Cell Biology 93, 839848.CrossRefGoogle Scholar