Current topics in the regulatory mechanism underlying the Ca2+ sensitization of the contractile apparatus in vascular smooth muscle
被引:121
作者:
Hirano, Katsuya
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机构:
Kyushu Univ, Grad Sch Med Sci, Div Mol Cardiol, Res Inst Angiocardiol, Fukuoka 8128582, JapanKyushu Univ, Grad Sch Med Sci, Div Mol Cardiol, Res Inst Angiocardiol, Fukuoka 8128582, Japan
Hirano, Katsuya
[1
]
机构:
[1] Kyushu Univ, Grad Sch Med Sci, Div Mol Cardiol, Res Inst Angiocardiol, Fukuoka 8128582, Japan
vascular smooth muscle;
contraction;
calcium;
Ca2+ sensitivity;
signal transduction;
D O I:
10.1254/jphs.CP0070027
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
The Ca2+ signal is the primary determinant of the contraction of the vascular smooth muscle. However, the alteration of the Ca2+ sensitivity of the contractile apparatus also plays an essential role. The regulation of the myosin light chain phosphatase (MLCP) activity is considered to be the most important mechanism underlying the regulation of Ca2+ sensitivity. The investigations during the last 15 years have identified many proteins that participate in the regulation of the MLCP activity. Recently, the Ca2+ signal has also been shown to cross-talk with the mechanisms regulating the Ca2+ sensitivity. Consequently, Rho kinase, protein kinase C, CPI-17, and MYPT1 have all been suggested to play a physiologically important role in the regulation of the MLCP activity. We are now close to elucidating the major rules regulating the MLCP activity and the Ca2+ sensitivity during vascular contractions. This article will give an overview of the current understanding of the biochemical basis for the regulation of the MLCP activity, while also discussing their functional roles from a physiological point of view. I hope this article will help to develop new pharmacological strategies for the prevention and treatment of the pathological vasoconstriction often seen in vascular diseases.
机构:
Kyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, JapanKyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, Japan
Bi, D
Nishimura, J
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Kyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, JapanKyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, Japan
Nishimura, J
Niiro, N
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Kyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, JapanKyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, Japan
Niiro, N
Hirano, K
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Kyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, JapanKyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, Japan
Hirano, K
Kanaide, H
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Kyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, JapanKyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, Japan
机构:
Kyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, JapanKyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, Japan
Bi, D
Nishimura, J
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h-index: 0
机构:
Kyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, JapanKyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, Japan
Nishimura, J
Niiro, N
论文数: 0引用数: 0
h-index: 0
机构:
Kyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, JapanKyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, Japan
Niiro, N
Hirano, K
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机构:
Kyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, JapanKyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, Japan
Hirano, K
Kanaide, H
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h-index: 0
机构:
Kyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, JapanKyushu Univ, Grad Sch Med Sci, Angiocardiol Res Inst, Div Mol Cardiol, Fukuoka 812, Japan