TY - JOUR
T1 - Calcium signaling in smooth muscle
AU - Nelson, Mark
AU - Hill-Eubanks, David C.
AU - Werner, Matthias E.
AU - Heppner, Thomas J.
AU - Nelson, Mark T.
N1 - P01 HL077378, NHLBI NIH HHS, United StatesP20 R016435, PHS HHS, United StatesPG/07/115, British Heart Foundation, United KingdomR01 DK065947, NIDDK NIH HHS, United StatesR01 HL098243, NHLBI NIH HHS, United StatesR01 HL44455, NHLBI NIH HHS, United StatesR37 DK053832-14, NIDDK NIH HHS, United StatesR37DK053832, NIDDK NIH HHS, United States
PY - 2011/9
Y1 - 2011/9
N2 - Changes in intracellular Ca2+ are central to the function of smooth muscle, which lines the walls of all hollow organs. These changes take a variety of forms, from sustained, cell-wide increases to temporally varying, localized changes. The nature of the Ca2+ signal is a reflection of the source of Ca2+ (extracellular or intracellular) and the molecular entity responsible for generating it. Depending on the specific channel involved and the detection technology employed, extracellular Ca2+ entry may be detected optically as graded elevations in intracellular Ca2+, junctional Ca2+ transients, Ca2+ flashes, or Ca2+ sparklets,whereas release of Ca2+ from intracellular stores may manifest as Ca2+ sparks, Ca2+ puffs, or Ca2+waves. These diverse Ca2+ signals collectively regulate a variety of functions. Some functions, such as contractility, are unique to smooth muscle; others are common to other excitable cells (e.g., modulation of membrane potential) and nonexcitable cells (e.g., regulation of gene expression). © 2011 Cold Spring Harbor Laboratory Press.
AB - Changes in intracellular Ca2+ are central to the function of smooth muscle, which lines the walls of all hollow organs. These changes take a variety of forms, from sustained, cell-wide increases to temporally varying, localized changes. The nature of the Ca2+ signal is a reflection of the source of Ca2+ (extracellular or intracellular) and the molecular entity responsible for generating it. Depending on the specific channel involved and the detection technology employed, extracellular Ca2+ entry may be detected optically as graded elevations in intracellular Ca2+, junctional Ca2+ transients, Ca2+ flashes, or Ca2+ sparklets,whereas release of Ca2+ from intracellular stores may manifest as Ca2+ sparks, Ca2+ puffs, or Ca2+waves. These diverse Ca2+ signals collectively regulate a variety of functions. Some functions, such as contractility, are unique to smooth muscle; others are common to other excitable cells (e.g., modulation of membrane potential) and nonexcitable cells (e.g., regulation of gene expression). © 2011 Cold Spring Harbor Laboratory Press.
U2 - 10.1101/cshperspect.a004549
DO - 10.1101/cshperspect.a004549
M3 - Article
C2 - 21709182
SN - 1943-0264
VL - 3
SP - 1
EP - 20
JO - Cold Spring Harbor Perspectives in Biology
JF - Cold Spring Harbor Perspectives in Biology
IS - 9
ER -