Improved superfusion technique for rapid cooling or heating of cultured cells under patch-clamp conditions
Language English Country Netherlands Media print-electronic
Document type Evaluation Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
16129494
DOI
10.1016/j.jneumeth.2005.07.005
PII: S0165-0270(05)00265-7
Knihovny.cz E-resources
- MeSH
- Action Potentials physiology MeSH
- Equipment Failure Analysis MeSH
- Cell Culture Techniques instrumentation methods MeSH
- Equipment Design MeSH
- Rats MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Membrane Potentials physiology MeSH
- Patch-Clamp Techniques instrumentation methods MeSH
- Neurons, Afferent physiology MeSH
- Cold Temperature * MeSH
- Perfusion instrumentation MeSH
- Environment, Controlled MeSH
- Hot Temperature * MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Evaluation Study MeSH
- Research Support, Non-U.S. Gov't MeSH
We have developed an improved technique for fast cooling and heating of solutions superfusing isolated cells under patch-clamp or calcium imaging conditions. The system meets the requirements for studying temperature dependency of all kinds of ion channels, in particular temperature-gated ion channels. It allows the application of temperature changes within a range of 5-60 degrees C at maximum rates of -40 degrees C/s to 60 degrees C/s. Barrels filled with different solutions are connected to a manifold consisting of seven silica capillaries (320 microm inner diameter, i.d.). A common outlet consists of a glass capillary through which the solutions are applied onto the cell surface. The upper part of this capillary is embedded in a temperature exchanger driven by a miniature Peltier device which preconditions the temperature of the passing solution. The lower part of the capillary carries an insulated copper wire, densely coiled over a length of 7 mm, and connected to a dc current source for resistive heating. The Peltier device and the heating element are electrically connected to the headstage probe which is fixed on to a micromanipulator for positioning of the manifold. The temperature of the flowing solution is measured by a miniature thermocouple inserted into the common outlet capillary near to its orifice which is placed at a distance of less than 100 microm from the surface of the examined cell. The temperature is either manually controlled by voltage commands or adjusted via the digital-to-analog converter of a conventional data acquisition interface. Examples are given of using the device in patch-clamp studies on heterologously expressed TRPV1, TRPM8, and on cultured rat sensory neurons.
References provided by Crossref.org
Cannabinoid non-cannabidiol site modulation of TRPV2 structure and function
Structural mechanism of heat-induced opening of a temperature-sensitive TRP channel
Human and Mouse TRPA1 Are Heat and Cold Sensors Differentially Tuned by Voltage
Cytoplasmic Inter-Subunit Interface Controls Use-Dependence of Thermal Activation of TRPV3 Channel
Heat-resistant action potentials require TTX-resistant sodium channels NaV1.8 and NaV1.9
The human transient receptor potential vanilloid 3 channel is sensitized via the ERK pathway
N-terminal tetrapeptide T/SPLH motifs contribute to multimodal activation of human TRPA1 channel
Amplified cold transduction in native nociceptors by M-channel inhibition
Potentiation of inhibitory synaptic transmission by extracellular ATP in rat suprachiasmatic nuclei
The C-terminal basic residues contribute to the chemical- and voltage-dependent activation of TRPA1