AI Article Synopsis

  • - This study explores the single-channel properties of different nicotinic acetylcholine receptors (nAChRs) by using knockout mice that lack specific receptor subunits, leading to clearer measurements in superior cervical ganglion neurons.
  • - Researchers found that α3β4 receptors exhibited a principal conductance level of 32.6 pS, while α3β4α5 receptors had similar conductance but with longer open and burst durations, contrasting with the lower conductance of α3β4β2 receptors at 13.6 pS.
  • - This work is significant because it provides the first detailed characterization of these distinct neuronal nAChRs' single-channel properties in their natural settings, enhancing understanding of their functional roles.

Article Abstract

Previous attempts to measure the functional properties of recombinant nicotinic acetylcholine receptors (nAChRs) composed of known receptor subunits have yielded conflicting results. The use of knockout mice that lack α5, β2, α5β2 or α5β2α7 nAChR subunits enabled us to measure the single-channel properties of distinct α3β4, α3β4α5 and α3β4β2 receptors in superior cervical ganglion (SCG) neurons. Using this approach, we found that α3β4 receptors had a principal conductance level of 32.6 ± 0.8 pS (mean ± SEM) and both higher and lower secondary conductance levels. α3β4α5 receptors had the same conductance as α3β4 receptors, but differed from α3β4 receptors by having an increased channel open time and increased burst duration. By contrast, α3β4β2 receptors differed from α3β4 and α3β4α5 receptors by having a significantly smaller conductance level (13.6 ± 0.5 pS). After dissecting the single-channel properties of these receptors using our knockout models, we then identified these properties - and hence the receptors themselves - in wild-type SCG neurons. This study is the first to identify the single-channel properties of distinct neuronal nicotinic receptors in their native environment.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3717227PMC
http://dx.doi.org/10.1113/jphysiol.2012.246595DOI Listing

Publication Analysis

Top Keywords

single-channel properties
16
α3β4 α3β4α5
12
nicotinic acetylcholine
12
receptors
12
α3β4 receptors
12
α3β4α5 α3β4β2
8
acetylcholine receptors
8
receptor subunits
8
properties distinct
8
α3β4β2 receptors
8

Similar Publications

Efficient single-channel current measurements of the human BK channel using a liposome-immobilized gold probe.

Anal Sci

December 2024

Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University, 3-1-1 Tsushima-naka, Kita-ku, Okayama-shi, Okayama, 700-8530, Japan.

The human BK channel (hBK) is an essential membrane protein that regulates various biological functions, and its dysfunction leads to serious diseases. Understanding the biophysical properties of hBK channels is crucial for drug development. Artificial lipid bilayer recording is used to measure biophysical properties at the single-channel level.

View Article and Find Full Text PDF

The Drosophila neuromuscular junction (NMJ) is a powerful genetic system that has revealed numerous conserved mechanisms for synapse development and homeostasis. The fly NMJ uses glutamate as the excitatory neurotransmitter and relies on kainate-type glutamate receptors and their auxiliary protein Neto for synapse assembly and function. However, despite decades of study, the reconstitution of NMJ glutamate receptors using heterologous systems has been achieved only recently, and there are no reports on the gating properties for the recombinant receptors.

View Article and Find Full Text PDF

Bioinspired Magnetized String with Tension-Dependent Eigenfrequencies for Wearable Human-Machine Interactions.

ACS Appl Mater Interfaces

December 2024

Joint Key Laboratory of the Ministry of Education, Institute of Applied Physics and Materials Engineering, University of Macau, Avenida da Universidade, Taipa, Macau 999078, P.R. China.

Article Synopsis
  • Flexible and wearable devices are proving useful for human-machine interactions (HMIs) and the Internet of Things, but there's a need for better communication storage and simpler designs.
  • A new approach inspired by natural tendons uses magnetized strings to detect vibrations; the strings' unique frequencies send signals through a single channel, allowing for multiple commands.
  • This method allows for customizable interactions by adjusting string tension, demonstrating potential use in areas like authentication, robotics, and other multifunctional applications.
View Article and Find Full Text PDF
Article Synopsis
  • - Gap junction intercellular communication is vital for various bodily functions, and is created when two hemichannels from adjacent cells dock together.
  • - This study focused on the properties of heterotypic gap junctions made from Cx46 and Cx50, revealing that magnesium (Mg) influences their conductance, showing changes depending on Mg presence.
  • - A specific genetic variant in Cx46 (E43F) altered the conductance response to Mg, suggesting that understanding magnesium's effects could lead to insights into gap junction communication in health and disease.
View Article and Find Full Text PDF

Stable oxidative posttranslational modifications alter the gating properties of RyR1.

J Gen Physiol

December 2024

Department of Physiology and Pharmacology, Molecular Muscle Physiology and Pathophysiology lab, Karolinska Institutet, Stockholm, Sweden.

The ryanodine receptor type 1 (RyR1) is a Ca2+ release channel that regulates skeletal muscle contraction by controlling Ca2+ release from the sarcoplasmic reticulum (SR). Posttranslational modifications (PTMs) of RyR1, such as phosphorylation, S-nitrosylation, and carbonylation are known to increase RyR1 open probability (Po), contributing to SR Ca2+ leak and skeletal muscle dysfunction. PTMs on RyR1 have been linked to muscle dysfunction in diseases like breast cancer, rheumatoid arthritis, Duchenne muscle dystrophy, and aging.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!