Hostname: page-component-78c5997874-t5tsf Total loading time: 0 Render date: 2024-11-05T01:04:22.112Z Has data issue: false hasContentIssue false

Photoreceptor cells with unusual functional properties on the ventral nerve of Limulus

Published online by Cambridge University Press:  07 July 2001

KÁROLY NAGY
Affiliation:
Institut für Biologie II, RWTH Aachen, Kopernikusstr. 16, D-52074 Aachen, Germany
MARLIES DORLÖCHTER
Affiliation:
Institut für Biologie II, RWTH Aachen, Kopernikusstr. 16, D-52074 Aachen, Germany Present address: Institut für Zoophysiologie, Universität Bonn, Endenicher Allee 11-13, 53115 Bonn, Germany.
SVENJA KLÄSEN
Affiliation:
Institut für Biologie II, RWTH Aachen, Kopernikusstr. 16, D-52074 Aachen, Germany
DANNY STEINBUSCH
Affiliation:
Institut für Biologie II, RWTH Aachen, Kopernikusstr. 16, D-52074 Aachen, Germany

Abstract

Normal photoreceptor cells on the ventral nerve of Limulus respond to a moderately intense flash with a large receptor potential or current. Occasionally, cells are found in which the same flash evokes only a small receptor potential or current. Our investigations reveal physiological reasons for the poor light sensitivity in these “unusual cells.” In unusual cells prolonged illumination with intense light evokes a step-like inward current with an amplitude of some nanoamperes, but without a large transient peak. The current appears to be summed up of single photon responses with amplitudes smaller than about 50 pA. Their time course is similar to that of small single photon responses forming the so-called macroscopic C1 component in normal cells. The macroscopic current evoked by an intense flash has slow activation and deactivation kinetics and reaches a saturated amplitude of about 4–5 nanoamperes. The light-intensity dependence of the current evoked by flashes or by prolonged illumination has a slope of about 1 in log–log plots. The decay kinetics of the current is similar to that of the C1 component measured in normal cells after the block of the C2 component. Occasionally, the step-like current is superposed by large standard bumps. These bumps are blocked by the Ca2+-ATPase inhibitor cyclopiazonic acid, while the sustained inward current persists. We conclude that in unusual cells the light-activated current is identical to the C1 component of normal cells. The phospholipase C pathway that in normal cells presumably gives rise to the C2 component functions only with a low efficiency in unusual cells.

Type
Research Article
Copyright
1999 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)