전단 자극에 의한 심방 근세포 칼슘 웨이브의 발생 : Phospholipase C-이노시톨 1,4,5-삼인산 수용체 신호전달의 역할

Cardiac myocytes are subjected to fluid shear stress during each contraction and relaxation. Under pathological conditions, such as valve disease, heart failure or hypertension, shear stress in cardiac chamber increases due to high blood volume and pressure. The shear stress induces proarrhythmic lo...

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Published inYaghag-hoi-ji Vol. 59; no. 4; pp. 158 - 163
Main Authors 김준철(Joon-Chul Kim), 우선희(Sun-Hee Woo)
Format Journal Article
LanguageKorean
Published The Pharmaceutical Society Of Korea 31.08.2015
대한약학회
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ISSN0377-9556
2383-9457

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Abstract Cardiac myocytes are subjected to fluid shear stress during each contraction and relaxation. Under pathological conditions, such as valve disease, heart failure or hypertension, shear stress in cardiac chamber increases due to high blood volume and pressure. The shear stress induces proarrhythmic longitudinal global $Ca^{2+}$ waves in atrial myocytes. In the present study, we further explored underlying cellular mechanism for the shear stress-induced longitudinal global $Ca^{2+}$ wave in isolated rat atrial myocytes. A shear stress of ${\sim}16dyn/cm^2$ was applied onto entire single myocyte using pressurized fluid puffing. Confocal $Ca^{2+}$ imaging was performed to measure local and global $Ca^{2+}$ signals. Shear stress elicited longitudinally propagating global $Ca^{2+}$ wave (${\sim}80{\mu}m/s$). The occurrence of shear stress-induced atrial $Ca^{2+}$ wave was eliminated by the inhibition of ryanodine receptors (RyRs) or inositol 1,4,5-trisphosphate receptors ($IP_3Rs$). In addition, pretreatment of phospholipase C (PLC) inhibitor U73122, but not its inactive analogue U73343, abolished the generation of longitudinal $Ca^{2+}$ wave under shear stress. Our data suggest that shear-induced longitudinal $Ca^{2+}$ wave may be induced by $Ca^{2+}$-induced $Ca^{2+}$ release through the RyRs which is triggered by $PLC-IP_3R$ signaling in atrial myocytes.
AbstractList Cardiac myocytes are subjected to fluid shear stress during each contraction and relaxation. Under pathologicalconditions, such as valve disease, heart failure or hypertension, shear stress in cardiac chamber increases due to high bloodvolume and pressure. The shear stress induces proarrhythmic longitudinal global Ca2+ waves in atrial myocytes. In thepresent study, we further explored underlying cellular mechanism for the shear stress-induced longitudinal global Ca2+wave in isolated rat atrial myocytes. A shear stress of ~16 dyn/cm2 was applied onto entire single myocyte using pressurizedfluid puffing. Confocal Ca2+ imaging was performed to measure local and global Ca2+ signals. Shear stress elicitedlongitudinally propagating global Ca2+ wave (~80 μm/s). The occurrence of shear stress-induced atrial Ca2+ wave was eliminatedby the inhibition of ryanodine receptors (RyRs) or inositol 1,4,5-trisphosphate receptors (IP3Rs). In addition, pretreatmentof phospholipase C (PLC) inhibitor U73122, but not its inactive analogue U73343, abolished the generation of longitudinalCa2+ wave under shear stress. Our data suggest that shear-induced longitudinal Ca2+ wave may be induced byCa2+-induced Ca2+ release through the RyRs which is triggered by PLC-IP3R signaling in atrial myocytes. KCI Citation Count: 0
Cardiac myocytes are subjected to fluid shear stress during each contraction and relaxation. Under pathological conditions, such as valve disease, heart failure or hypertension, shear stress in cardiac chamber increases due to high blood volume and pressure. The shear stress induces proarrhythmic longitudinal global $Ca^{2+}$ waves in atrial myocytes. In the present study, we further explored underlying cellular mechanism for the shear stress-induced longitudinal global $Ca^{2+}$ wave in isolated rat atrial myocytes. A shear stress of ${\sim}16dyn/cm^2$ was applied onto entire single myocyte using pressurized fluid puffing. Confocal $Ca^{2+}$ imaging was performed to measure local and global $Ca^{2+}$ signals. Shear stress elicited longitudinally propagating global $Ca^{2+}$ wave (${\sim}80{\mu}m/s$). The occurrence of shear stress-induced atrial $Ca^{2+}$ wave was eliminated by the inhibition of ryanodine receptors (RyRs) or inositol 1,4,5-trisphosphate receptors ($IP_3Rs$). In addition, pretreatment of phospholipase C (PLC) inhibitor U73122, but not its inactive analogue U73343, abolished the generation of longitudinal $Ca^{2+}$ wave under shear stress. Our data suggest that shear-induced longitudinal $Ca^{2+}$ wave may be induced by $Ca^{2+}$-induced $Ca^{2+}$ release through the RyRs which is triggered by $PLC-IP_3R$ signaling in atrial myocytes.
Author 김준철(Joon-Chul Kim)
우선희(Sun-Hee Woo)
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DocumentTitleAlternate Activation of a Ca2+ wave by Shear Stress in Atrial Myocytes : Role of Phospholipase C-inositol 1,4,5-Trisphosphate Receptor Signaling
Activation of a Ca2+ wave by Shear Stress in Atrial Myocytes: Role of Phospholipase C-inositol 1,4,5-Trisphosphate Receptor Signaling
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Keywords phospholipase C
shear stress
4
5-trisphosphate receptor
atrial myocytes
longitudinal Ca2+ wave
inositol 1
inositol 1,4,5-trisphosphate receptor
longitudinal $Ca^{2+}$ wave
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Title 전단 자극에 의한 심방 근세포 칼슘 웨이브의 발생 : Phospholipase C-이노시톨 1,4,5-삼인산 수용체 신호전달의 역할
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