Exogenous expression of an allatotropin-related peptide receptor increased the membrane excitability in Aplysia neurons.

Aplysia Electrophysiology G-protein coupled receptors Neuronal excitability Neuropeptide Plasmid microinjection

Journal

Molecular brain
ISSN: 1756-6606
Titre abrégé: Mol Brain
Pays: England
ID NLM: 101468876

Informations de publication

Date de publication:
09 05 2022
Historique:
received: 04 04 2022
accepted: 01 05 2022
entrez: 9 5 2022
pubmed: 10 5 2022
medline: 12 5 2022
Statut: epublish

Résumé

Neuropeptides act mostly on a class of G-protein coupled receptors, and play a fundamental role in the functions of neural circuits underlying behaviors. However, physiological functions of some neuropeptide receptors are poorly understood. Here, we used the molluscan model system Aplysia and microinjected the exogenous neuropeptide receptor apATRPR (Aplysia allatotropin-related peptide receptor) with an expression vector (pNEX3) into Aplysia neurons that did not express the receptor endogenously. Physiological experiments demonstrated that apATRPR could mediate the excitability increase induced by its ligand, apATRP (Aplysia allatotropin-related peptide), in the Aplysia neurons that now express the receptor. This study provides a definitive evidence for a physiological function of a neuropeptide receptor in molluscan animals.

Identifiants

pubmed: 35534865
doi: 10.1186/s13041-022-00929-4
pii: 10.1186/s13041-022-00929-4
pmc: PMC9082908
doi:

Substances chimiques

Insect Hormones 0
Neuropeptides 0
Receptors, Neuropeptide 0
allatotropin 75831-28-6

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

42

Informations de copyright

© 2022. The Author(s).

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Auteurs

Guo Zhang (G)

State Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China.

Shi-Qi Guo (SQ)

State Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China.

Si-Yuan Yin (SY)

State Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China.

Wang-Ding Yuan (WD)

State Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China.

Ping Chen (P)

State Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China.

Ji-Il Kim (JI)

School of Biological Sciences, Seoul National University, 1, Gwanak-ro, Gwanak-gu, Seoul, 08826, Korea.

Hui-Ying Wang (HY)

State Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China.

Hai-Bo Zhou (HB)

School of Electronic Science and Engineering, Nanjing University, Nanjing, 210023, Jiangsu, China.
Peng Cheng Laboratory, Shenzhen, 518000, China.

Abraham J Susswein (AJ)

The Mina and Everard Goodman Faculty of Life Sciences, Bar Ilan University, 52900, Ramat Gan, Israel.

Bong-Kiun Kaang (BK)

School of Biological Sciences, Seoul National University, 1, Gwanak-ro, Gwanak-gu, Seoul, 08826, Korea.

Jian Jing (J)

State Key Laboratory of Pharmaceutical Biotechnology, Institute for Brain Sciences, Advanced Institute for Life Sciences, School of Life Sciences, Nanjing University, Nanjing, 210023, Jiangsu, China. jingj01@live.com.
Peng Cheng Laboratory, Shenzhen, 518000, China. jingj01@live.com.
Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA. jingj01@live.com.

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Classifications MeSH