The Enterins: A Novel Family of Neuropeptides Isolated from the Enteric Nervous System and CNS of Aplysia
- 15 October 2001
- journal article
- Published by Society for Neuroscience in Journal of Neuroscience
- Vol. 21 (20), 8247-8261
- https://doi.org/10.1523/jneurosci.21-20-08247.2001
Abstract
To identify neuropeptides that have a broad spectrum of actions on the feeding system of Aplysia, we searched for bioactive peptides that are present in both the gut and the CNS. We identified a family of structurally related nonapeptides and decapeptides (enterins) that are present in the gut and CNS of Aplysia, and most of which share the HSFVamide sequence at the C terminus. The structure of the enterin precursor deduced from cDNA cloning predicts 35 copies of 20 different enterins. Northern analysis, in situhybridization, and immunocytochemistry show that the enterins are abundantly present in the CNS and the gut of Aplysia. Using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry we characterized the enterin-precursor processing, demonstrated that all of the precursor-predicted enterins are present, and determined post-translational modifications of various enterins. Enterin-positive neuronal somata and processes were found in the gut, and enterins inhibited contractions of the gut. In the CNS, the cerebral and buccal ganglia, which control feeding, contained the enterins. Enterin was also present in the nerve that connects these two ganglia. Enterins reduced the firing of interneurons B4/5 during feeding motor programs. Such enterin-induced reduction of firing also occurred when excitability of B4/5 was tested directly. Because reduction of B4/5 activity corresponds to a switch from egestive to ingestive behaviors, enterin may contribute to such program switching. Furthermore, because enterins are present throughout the nervous system, they may also play a regulatory role in nonfeeding behaviors ofAplysia.Keywords
This publication has 36 references indexed in Scilit:
- Analyzing the functional consequences of transmitter complexityTrends in Neurosciences, 1997
- A new technique for chronic single-unit extracellular recording in freely behaving animals using pipette electrodesJournal of Neuroscience Methods, 1995
- Structure, localization, and action of buccalin B: A bioactive peptide from AplysiaPeptides, 1994
- Rapid Communication: Neuropeptide Expression and Processing as Revealed by Direct Matrix‐Assisted Laser Desorption Ionization Mass Spectrometry of Single NeuronsJournal of Neurochemistry, 1994
- In situ hybridization of whole-mounts of Aplysia ganglia using non-radioactive probesJournal of Neuroscience Methods, 1992
- The Biosynthesis of Neuropeptides: Peptide alpha-AmidationAnnual Review of Neuroscience, 1992
- Structure, bioactivity, and cellular localization of myomodulin B: A novel Aplysia peptidePeptides, 1991
- Sequence of small cardioactive peptide A: A second member of a class of neuropeptides in AplysiaPeptides, 1987
- Aplysia neurons express a gene encoding multiple FMRFamide neuropeptidesCell, 1985
- Structure of a Molluscan Cardioexcitatory NeuropeptideScience, 1977