Transient receptor potential channels in mechanosensing and cell volume regulation.

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Transient receptor potential channels in mechanosensing and cell volume regulation. / Pedersen, Stine Falsig; Nilius, Bernd.

In: Methods in Enzymology, Vol. 428, 2007, p. 183-207.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Pedersen, SF & Nilius, B 2007, 'Transient receptor potential channels in mechanosensing and cell volume regulation.', Methods in Enzymology, vol. 428, pp. 183-207. https://doi.org/10.1016/S0076-6879(07)28010-3

APA

Pedersen, S. F., & Nilius, B. (2007). Transient receptor potential channels in mechanosensing and cell volume regulation. Methods in Enzymology, 428, 183-207. https://doi.org/10.1016/S0076-6879(07)28010-3

Vancouver

Pedersen SF, Nilius B. Transient receptor potential channels in mechanosensing and cell volume regulation. Methods in Enzymology. 2007;428:183-207. https://doi.org/10.1016/S0076-6879(07)28010-3

Author

Pedersen, Stine Falsig ; Nilius, Bernd. / Transient receptor potential channels in mechanosensing and cell volume regulation. In: Methods in Enzymology. 2007 ; Vol. 428. pp. 183-207.

Bibtex

@article{bebc1cc0909c11dd86a6000ea68e967b,
title = "Transient receptor potential channels in mechanosensing and cell volume regulation.",
abstract = "Transient receptor potential (TRP) channels are unique cellular sensors responding to a wide variety of extra- and intracellular signals, including mechanical and osmotic stress. In recent years, TRP channels from multiple subfamilies have been added to the list of mechano- and/or osmosensitive channels, and it is becoming increasingly apparent that Ca(2+) influx via TRP channels plays a crucial role in the response to mechanical and osmotic perturbations in a wide range of cell types. Although the events translating mechanical and osmotic stimuli into regulation of TRP channels are still incompletely understood, the specific mechanisms employed vary between different TRP isoforms, and probably include changes in the tension and/or curvature of the lipid bilayer, changes in the cortical cytoskeleton, and signaling events such as lipid metabolism and protein phosphorylation/dephosphorylation. This chapter describes candidate mechanosensitive channels from mammalian TRP subfamilies, discusses inherent and technical issues potentially confounding evaluation of mechano- and/or osmosensitivity, and presents methods relevant to the study of TRP channel regulation by mechanical and osmotic stimuli and involvement in cell volume regulation.",
author = "Pedersen, {Stine Falsig} and Bernd Nilius",
note = "Keywords: Animals; CHO Cells; Calcium; Cell Size; Cricetinae; Cricetulus; Humans; Mechanotransduction, Cellular; Membrane Proteins; Mice; Osmotic Pressure; Patch-Clamp Techniques; TRPM Cation Channels; TRPV Cation Channels; Transient Receptor Potential Channels",
year = "2007",
doi = "10.1016/S0076-6879(07)28010-3",
language = "English",
volume = "428",
pages = "183--207",
journal = "Methods in Enzymology",
issn = "0076-6879",
publisher = "Academic Press",

}

RIS

TY - JOUR

T1 - Transient receptor potential channels in mechanosensing and cell volume regulation.

AU - Pedersen, Stine Falsig

AU - Nilius, Bernd

N1 - Keywords: Animals; CHO Cells; Calcium; Cell Size; Cricetinae; Cricetulus; Humans; Mechanotransduction, Cellular; Membrane Proteins; Mice; Osmotic Pressure; Patch-Clamp Techniques; TRPM Cation Channels; TRPV Cation Channels; Transient Receptor Potential Channels

PY - 2007

Y1 - 2007

N2 - Transient receptor potential (TRP) channels are unique cellular sensors responding to a wide variety of extra- and intracellular signals, including mechanical and osmotic stress. In recent years, TRP channels from multiple subfamilies have been added to the list of mechano- and/or osmosensitive channels, and it is becoming increasingly apparent that Ca(2+) influx via TRP channels plays a crucial role in the response to mechanical and osmotic perturbations in a wide range of cell types. Although the events translating mechanical and osmotic stimuli into regulation of TRP channels are still incompletely understood, the specific mechanisms employed vary between different TRP isoforms, and probably include changes in the tension and/or curvature of the lipid bilayer, changes in the cortical cytoskeleton, and signaling events such as lipid metabolism and protein phosphorylation/dephosphorylation. This chapter describes candidate mechanosensitive channels from mammalian TRP subfamilies, discusses inherent and technical issues potentially confounding evaluation of mechano- and/or osmosensitivity, and presents methods relevant to the study of TRP channel regulation by mechanical and osmotic stimuli and involvement in cell volume regulation.

AB - Transient receptor potential (TRP) channels are unique cellular sensors responding to a wide variety of extra- and intracellular signals, including mechanical and osmotic stress. In recent years, TRP channels from multiple subfamilies have been added to the list of mechano- and/or osmosensitive channels, and it is becoming increasingly apparent that Ca(2+) influx via TRP channels plays a crucial role in the response to mechanical and osmotic perturbations in a wide range of cell types. Although the events translating mechanical and osmotic stimuli into regulation of TRP channels are still incompletely understood, the specific mechanisms employed vary between different TRP isoforms, and probably include changes in the tension and/or curvature of the lipid bilayer, changes in the cortical cytoskeleton, and signaling events such as lipid metabolism and protein phosphorylation/dephosphorylation. This chapter describes candidate mechanosensitive channels from mammalian TRP subfamilies, discusses inherent and technical issues potentially confounding evaluation of mechano- and/or osmosensitivity, and presents methods relevant to the study of TRP channel regulation by mechanical and osmotic stimuli and involvement in cell volume regulation.

U2 - 10.1016/S0076-6879(07)28010-3

DO - 10.1016/S0076-6879(07)28010-3

M3 - Journal article

C2 - 17875418

VL - 428

SP - 183

EP - 207

JO - Methods in Enzymology

JF - Methods in Enzymology

SN - 0076-6879

ER -

ID: 6382299