Journal
JOURNAL OF EXPERIMENTAL BIOLOGY
Volume 209, Issue 14, Pages 2749-2764Publisher
COMPANY BIOLOGISTS LTD
DOI: 10.1242/jeb.02312
Keywords
Titonia diomedea; dopamine; ciliary beat frequency; Ca2+ activated Cl- current
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Funding
- NINDS NIH HHS [5 F31 NS047922-02, F31 NS047922] Funding Source: Medline
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The physiological mechanisms controlling ciliary beating remain largely unknown. Evidence exists supporting both hormonal control of ciliary beating and control via direct innervation. In the present study we investigated nervous control of cilia based locomotion in the nudibranch mollusc, Tritonia diomedea. Ciliated pedal epithelial (CPE) cells acting as locomotory effectors may be electrically excitable. To explore this possibility we characterized the cells' electrical properties, and found that CPE cells have large voltage dependent whole cell currents with two components. First, there is a fast activating outward Cl- current that is both voltage and Ca2+ influx dependent (I-Cl(Ca)). I-Cl(Ca) is sensitive to DIDS and 9-AC, and resembles currents of Ca2+-activated Cl channels (CaCC). Ca2+ dependence also suggests the presence of voltage-gated Ca2+ channels; however, we were unable to detect these currents. The second current, a voltage dependent proton current (I-H), activates very slowly and is sensitive to both Zn2+ and changes in pH. In addition we identify a new cilio-excitatory substance in Tritonia, viz., dopamine. Dopamine, in the 10 mu mol l(-1)-1 mmol l(-1) range, significantly increases ciliary beat frequency (CBF). We also found dopamine and Tritonia Pedal Peptide (TPep-NLS) selectively suppress ICl( Ca) in CPE cells, demonstrating a link between CBF excitation and ICl( Ca). It appears that dopamine and TPep-NLS inhibit ICl( Ca) not through changing [Ca2+] in, but directly by an unknown mechanism. Coupling of ICl(Ca) and CBF is further supported by our finding that DIDS and zero [Cl-] out both increase CBF, mimicking dopamine and TPep-NLS excitation. These results suggest that dopamine and TPep-NLS act to inhibit ICl(Ca), initiating and prolonging Ca2+ influx, and activating CBF excitation.
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