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Inhibition of cholinergic pathways in Drosophila melanogaster by ?-conotoxins.

ABSTRACT: Nicotinic acetylcholine receptors (nAChRs) play a pivotal role in synaptic transmission of neuronal signaling pathways and are fundamentally involved in neuronal disorders, including Alzheimer's disease, Parkinson's disease, and schizophrenia. In vertebrates, cholinergic pathways can be selectively inhibited by ?-conotoxins; we show that in the model organism Drosophila, the cholinergic component of the giant fiber system is inhibited by ?-conotoxins MII, AuIB, BuIA, EI, PeIA, and ImI. The injection of 45 pmol/fly of each toxin dramatically decreases the response of the giant fiber to dorsal longitudinal muscle (GF-DLM) connection to 20 ± 13.9% for MII; 26 ± 13.7% for AuIB, 12 ± 9.9% for BuIA, 30 ± 11.3% for EI, 1 ± 1% for PeIA, and 34 ± 15.4% for ImI. Through bioassay-guided fractionation of the venom of Conus brunneus, we found BruIB, an ?-conotoxin that inhibits Drosophila nicotinic receptors but not its vertebrate counterparts. GF-DLM responses decreased to 43.7 ± 8.02% on injection of 45 pmol/fly of BruIB. We manipulated the D?7 nAChR to mimic the selectivity of its vertebrate counterpart by placing structurally guided point mutations in the conotoxin-binding site. This manipulation rendered vertebrate-like behavior in the Drosophila system, enhancing the suitability of Drosophila as an in vivo tool to carry out studies related to human neuronal diseases. .

SUBMITTER: Heghinian MD

PROVIDER: S-EPMC4422358 | biostudies-literature | 2015 Mar

REPOSITORIES: biostudies-literature

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Inhibition of cholinergic pathways in Drosophila melanogaster by α-conotoxins.

Heghinian Mari D MD Mejia Monica M Adams David J DJ Godenschwege Tanja A TA Marí Frank F

FASEB journal : official publication of the Federation of American Societies for Experimental Biology 20141202 3

Nicotinic acetylcholine receptors (nAChRs) play a pivotal role in synaptic transmission of neuronal signaling pathways and are fundamentally involved in neuronal disorders, including Alzheimer's disease, Parkinson's disease, and schizophrenia. In vertebrates, cholinergic pathways can be selectively inhibited by α-conotoxins; we show that in the model organism Drosophila, the cholinergic component of the giant fiber system is inhibited by α-conotoxins MII, AuIB, BuIA, EI, PeIA, and ImI. The injec ...[more]

PMID: 25466886

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Project description:Nicotinic acetylcholine receptors (nAChRs) are pentameric ligand-gated ion channels. The ?7 subtype of nAChRs is involved in neurological pathologies such as Parkinson's disease, Alzheimer's disease, addiction, epilepsy and autism spectrum disorders. The Drosophila melanogaster ?7 (D?7) has the closest sequence homology to the vertebrate ?7 subunit and it can form homopentameric receptors just as the vertebrate counterpart. The D?7 subunits are essential for the function of the Giant Fiber circuit, which mediates the escape response of the fly. To further characterize the receptor function, we generated different missense mutations in the D?7 nAChR's ligand binding domain. We characterized the effects of targeted expression of two UAS-constructs carrying a single mutation, D197A and Y195T, as well as a UAS-construct carrying a triple D77T, L117Q, I196P mutation in a D?7 null mutant and in a wild type background. Expression of the triple mutation was able to restore the function of the circuit in D?7 null mutants and had no disruptive effects when expressed in wild type. In contrast, both single mutations severely disrupted the synaptic transmission of D?7-dependent but not glutamatergic or gap junction dependent synapses in wild type background, and did not or only partially rescued the synaptic defects of the null mutant. These observations are consistent with the formation of hybrid receptors, consisting of D197A or Y195T subunits and wild type D?7 subunits, in which the binding of acetylcholine or acetylcholine-induced conformational changes of the D?7 receptor are altered and causes inhibition of cholinergic responses. Thus targeted expression of D197A or Y195T can be used to selectively disrupt synaptic transmission of D?7-dependent synapses in neuronal circuits. Hence, these constructs can be used as tools to study learning and memory or addiction associated behaviors by allowing the manipulation of neuronal processing in the circuits without affecting other cellular signaling.

Dataset Information

Inhibition of cholinergic pathways in Drosophila melanogaster by ?-conotoxins.

Publications

Inhibition of cholinergic pathways in Drosophila melanogaster by α-conotoxins.

Similar Datasets

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