Signaling of pigment-dispersing factor (PDF) in the Madeira cockroach Rhyparobia maderae

PLoS One. 2014 Sep 30;9(9):e108757. doi: 10.1371/journal.pone.0108757. eCollection 2014.

Abstract

The insect neuropeptide pigment-dispersing factor (PDF) is a functional ortholog of vasoactive intestinal polypeptide, the coupling factor of the mammalian circadian pacemaker. Despite of PDF's importance for synchronized circadian locomotor activity rhythms its signaling is not well understood. We studied PDF signaling in primary cell cultures of the accessory medulla, the circadian pacemaker of the Madeira cockroach. In Ca²⁺ imaging studies four types of PDF-responses were distinguished. In regularly bursting type 1 pacemakers PDF application resulted in dose-dependent long-lasting increases in Ca²⁺ baseline concentration and frequency of oscillating Ca²⁺ transients. Adenylyl cyclase antagonists prevented PDF-responses in type 1 cells, indicating that PDF signaled via elevation of intracellular cAMP levels. In contrast, in type 2 pacemakers PDF transiently raised intracellular Ca²⁺ levels even after blocking adenylyl cyclase activity. In patch clamp experiments the previously characterized types 1-4 could not be identified. Instead, PDF-responses were categorized according to ion channels affected. Application of PDF inhibited outward potassium or inward sodium currents, sometimes in the same neuron. In a comparison of Ca²⁺ imaging and patch clamp experiments we hypothesized that in type 1 cells PDF-dependent rises in cAMP concentrations block primarily outward K⁺ currents. Possibly, this PDF-dependent depolarization underlies PDF-dependent phase advances of pacemakers. Finally, we propose that PDF-dependent concomitant modulation of K⁺ and Na⁺ channels in coupled pacemakers causes ultradian membrane potential oscillations as prerequisite to efficient synchronization via resonance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine / analogs & derivatives
  • Adenine / pharmacology
  • Adenylyl Cyclase Inhibitors
  • Adenylyl Cyclases / metabolism
  • Animals
  • Benzazepines / pharmacology
  • Biological Clocks / drug effects
  • Biological Clocks / physiology*
  • Brain / cytology
  • Brain / drug effects
  • Brain / metabolism
  • Calcium / metabolism
  • Circadian Rhythm / drug effects
  • Circadian Rhythm / physiology
  • Cockroaches / drug effects
  • Cockroaches / physiology*
  • Cyclic AMP / metabolism
  • Enzyme Inhibitors / pharmacology
  • Insect Proteins / metabolism*
  • Insect Proteins / pharmacology
  • Ion Transport / drug effects
  • Membrane Potentials / drug effects
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / metabolism*
  • Neuropeptides / metabolism*
  • Neuropeptides / pharmacology
  • Patch-Clamp Techniques
  • Potassium / metabolism
  • Primary Cell Culture
  • Signal Transduction*
  • Sodium / metabolism
  • Tetrodotoxin / pharmacology

Substances

  • Adenylyl Cyclase Inhibitors
  • Benzazepines
  • Enzyme Inhibitors
  • Insect Proteins
  • Neuropeptides
  • DK-AH 268
  • 9-(tetrahydro-2-furyl)-adenine
  • Tetrodotoxin
  • Sodium
  • Cyclic AMP
  • Adenylyl Cyclases
  • Adenine
  • Potassium
  • Calcium

Grants and funding

This study was supported by DFG grants STE531/18-1,2 and STE 531/21-1 to MS. In addition, ESB is supported by a Ph.D. scholarship awarded by the Egyptian Ministry of Higher Education (MoHE) and the DAAD (Deutsche Akademischer Austauschdienst). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.