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Sensory Systems

Sensory neurobiology, the process by which selective sensory modalities -for example light, sound and smell- are transduced and coded by the nervous system, may seem an unlikely candidate for non-invasive electrochemical analysis. Sensory cells are frequently small and deeply embedded in organs and tissues. However, advances in our development of ltramicro-electrochemical sensors have allowed us to examine cells and structures down to approximately 10 µm diameter. This now includes rod and horizontal cells from the eye,1,10 as well as auditory hair cells,7 epithelial structures and, at a totally different scale, ion loss from the lymph in the olfactory sensilla of crustaceans.5,6

Vision research has had a long-standing history at the MBL, particularly with the use of the skate as a model. Collaborators with the BRC have used the self-referencing ion-selective technologies (SERIS), combined with single cell imaging, to address a controversial area in the field with regards to the role of proton concentration in the bulk media acting as a feedback modulator of horizontal cell function.1 Metabolic information has also been obtained from these cells, most recently as part of an ongoing study to assess the metabolic cost of signal processing (unpublished).

Related projects at the BRC

• Mechanisms of hair cell modulation >>
• Regulation of proton fluxes from retinal neurons >>

Related BRC publications

1) Molina, A.J.A., Verzi, M.P., Birnbaum, A.D., Yamoah, E.N., Hammar, K., Smith, P.J.S., Malchow, R.P. 2004. Neurotransmitter modulation of extracellular H+ fluxes from isolated retinal horizontal cells of the skate. Journal of Physiology-London 560:639-657.
2) Kreitzer, M.A., Andersen, K.A., Malchow, R.P. 2003 Glutamate modulation of GABA transport in retinal horizontal cells of the skate. Journal of Physiology-London, 546:717-731.
3) Molina, A.J.A., Hammar, K., Sanger R., Smith, P.J.S. and Malchow, R.P. 2003. Intracellular release of caged calcium in skate horizontal cells using fine optical fibers. Biological Bulletin, 205: 215-216.
4) Twig, G., Malchow, R.P., Hammar, K., Smith, P.J.S., Levy, H., Perlman,I. 2002. A novel turtle retinal preparation for simultaneously measuring light-induced electrical activity and changes in metabolite levels. Biological Bulletin, 203: 198-200.
5) Gleeson, R.A., Hammar, K. and Smith, P.J.S. 2000. Sustaining olfaction at low salinities: mapping ion flux associated with the olfactory sensilla of the blue crab Callinectes sapidus. Journal of Experimental Biology, 203: 3145-3152.
6) Gleeson, R.A., McDowell, L.M., Aldrich, H.C., Hammar, K. and Smith, P.J.S. 2000. Sustaining olfaction at low salinities: evidence for a paracellular route of ion movement from the hemolymph to the sensillar lymph in the olfactory sensillar of ther blue crab, Callinectes sapidus. Cell and Tissue Research 301: 423-431.
7) Yamoah, E., Lumpkin, E.A., Dumont, R.A., Smith, P.J.S., Hudspeth, A.J. and Gillespie, P.G. 1998. Plasma-membrane Ca2+-ATPase ensures low Ca2+ concentration in hair-cell stereocilia. Journal of Neuroscience. 18(2): 610-624.
8) Malchow, R.P., Verzi, M.P. and Smith, P.J.S. 1998. Extracellular pH gradients measured from isolated retinal cells. Biological Bulletin. 195: 203-204.
9) Andersen, K.A. and Malchow, R.P. 1998. Fluorometric analysis of intracellular sodium concentration in isolated retinal horizontal cells. Biological Bulletin, 195: 204-205.

10) Malchow, R.P., Land, S.C., Patel, L.S. and Smith, P.J.S. 1997. Consumption of oxygen by isolated skate retinal photoreceptors measured using a self-referencing oxygen-selective microelectrode. Biological Bulletin, 193: 231-232.

11) Malchow, R.P. and Smith, P.J.S. 1996. Ion fluxes from skate retinal horizontal cells measured using self-referencing ion-selective electrodes. Biological Bulletin, 191: 261-262.

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