Role of protein kinase D1 in vasoconstriction and haemodynamics in rats

Protein kinase D (PKD), once considered an effector of protein kinase C (PKC), now plays many pathophysiological roles in various tissues. However, little is known about role of PKD in vascular function. We investigated the role of PKD in contraction of rat aorta and human aortic smooth muscle cells...

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Veröffentlicht in:Microvascular research 2024-03, Vol.152, p.104627-104627, Article 104627
Hauptverfasser: Sugawara, Yoh, Mizuno, Yusuke, Oku, Shinya, Sawada, Yuri, Goto, Takahisa
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Mizuno, Yusuke
Oku, Shinya
Sawada, Yuri
Goto, Takahisa
description Protein kinase D (PKD), once considered an effector of protein kinase C (PKC), now plays many pathophysiological roles in various tissues. However, little is known about role of PKD in vascular function. We investigated the role of PKD in contraction of rat aorta and human aortic smooth muscle cells (HASMCs) and in haemodynamics in rats. Isometric tension of rat aortic was measured to examine norepinephrine-induced contraction in the presence of PKD, PKC and Rho-kinase inhibitors. Phosphorylation of PKD1, myosin targeting subunit-1 (MYPT1), myosin light chain (MLC), CPI-17 and heat-shock protein 27 (HSP27), and actin polymerization were measured in the aorta. Phosphorylation of MYPT1 and MLC was also measured in HASMCs knocked down with specific siRNAs of PKD 1, 2 and 3. Intracellular calcium concentrations and cell shortening were measured in HASMCs. Norepinephrine-induced aortic contraction was accompanied by increased phosphorylation of PKD1, MYPT1 and MLC and actin polymerization, all of which were attenuated with PKD inhibitor CRT0066101. PKD1 phosphorylation was not inhibited by PKC inhibitor, chelerythrine or Rho kinase inhibitor, fasudil. In HASMCs, the phosphorylation of MYPT1 and MLC was attenuated by PKD1, but not PKD2, 3 knockdown. In HASMCs, CRT0066101 inhibited norepinephrine-induced cell shortening without affecting calcium concentration. Administration of CRT0066101 decreased systemic vascular resistance and blood pressure without affecting cardiac output in rats. PKD1 may play roles in aorta contraction and haemodynamics via phosphorylation of MYPT1 and actin polymerization in a calcium-independent manner. •Little is known about role of Protein kinase D (PKD) in vascular function.•Norepinephrine increased phosphorylation of PKD1 during aortic contraction.•The phosphorylation of MYPT1 and MLC were attenuated with PKD-inhibitor and SiRNA.•PKD-inhibitor decreased cell shortening without change of calcium concentrations.•PKD1 might play roles in hemodynamics in a calcium-independent manner.
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However, little is known about role of PKD in vascular function. We investigated the role of PKD in contraction of rat aorta and human aortic smooth muscle cells (HASMCs) and in haemodynamics in rats. Isometric tension of rat aortic was measured to examine norepinephrine-induced contraction in the presence of PKD, PKC and Rho-kinase inhibitors. Phosphorylation of PKD1, myosin targeting subunit-1 (MYPT1), myosin light chain (MLC), CPI-17 and heat-shock protein 27 (HSP27), and actin polymerization were measured in the aorta. Phosphorylation of MYPT1 and MLC was also measured in HASMCs knocked down with specific siRNAs of PKD 1, 2 and 3. Intracellular calcium concentrations and cell shortening were measured in HASMCs. Norepinephrine-induced aortic contraction was accompanied by increased phosphorylation of PKD1, MYPT1 and MLC and actin polymerization, all of which were attenuated with PKD inhibitor CRT0066101. 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subjects Actin polymerization
Actins - metabolism
Animals
Calcium - metabolism
Haemodynamics
Humans
Intracellular calcium concentrations
Muscle Contraction
Muscle, Smooth, Vascular - metabolism
Myosin Light Chains - metabolism
MYPT1
Norepinephrine - metabolism
Norepinephrine - pharmacology
Phosphorylation
Protein kinase D1
Protein Kinase Inhibitors - pharmacology
Rats
rho-Associated Kinases - metabolism
Vasoconstriction
title Role of protein kinase D1 in vasoconstriction and haemodynamics in rats
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