TY - JOUR
T1 - High hydrostatic pressure induces slow contraction in mouse cardiomyocytes
AU - Yamaguchi, Yohei
AU - Nishiyama, Masayoshi
AU - Kai, Hiroaki
AU - Kaneko, Toshiyuki
AU - Kaihara, Keiko
AU - Iribe, Gentaro
AU - Takai, Akira
AU - Naruse, Keiji
AU - Morimatsu, Masatoshi
N1 - Funding Information:
The authors would like to thank Ms. Masumi Furutani (Central Research Laboratory, Okayama University Medical School, Japan) for technical assistance with the histological preparation for transmission electron microscopy and Dr. Masahiro Fujihashi for technical support. The authors also thank Dr. Armen Mekhdjian for reading our manuscript and Dr. Shinichi Ishiwata (Waseda University, Japan) and Dr. Toshiyuki Oda (University of Yamanashi, Japan) for helpful discussions. This work was funded by grants from the Japan Society for the Promotion of Science (JSPS KAKENHI Grant Numbers JP18K12033 , JP21K12645 , and JP21H05128 to M.M.; JP16K04908 , JP19H02566 , and JP22H01922 to M.N.; JP19K16485 and JP21K15338 to Y.Y.; JP21H04960 to K.N.), Innovative Science and Technology Initiative for Security Grant Number JPJ004596 to K.N., and the Akiyama Life Science Foundation (Grant No. 112-010) , Asahikawa Medical University grants for anti-aging research projects (Grant No. 30-8), and Suzuken Memorial Foundation (Grant No. 21-111) to Y.Y.
Funding Information:
The authors would like to thank Ms. Masumi Furutani (Central Research Laboratory, Okayama University Medical School, Japan) for technical assistance with the histological preparation for transmission electron microscopy and Dr. Masahiro Fujihashi for technical support. The authors also thank Dr. Armen Mekhdjian for reading our manuscript and Dr. Shinichi Ishiwata (Waseda University, Japan) and Dr. Toshiyuki Oda (University of Yamanashi, Japan) for helpful discussions. This work was funded by grants from the Japan Society for the Promotion of Science (JSPS KAKENHI Grant Numbers JP18K12033, JP21K12645, and JP21H05128 to M.M.; JP16K04908, JP19H02566, and JP22H01922 to M.N.; JP19K16485 and JP21K15338 to Y.Y.; JP21H04960 to K.N.), Innovative Science and Technology Initiative for Security Grant Number JPJ004596 to K.N. and the Akiyama Life Science Foundation (Grant No. 112-010), Asahikawa Medical University grants for anti-aging research projects (Grant No. 30-8), and Suzuken Memorial Foundation (Grant No. 21-111) to Y.Y. The authors declare no competing interests.
Publisher Copyright:
© 2022 Biophysical Society
PY - 2022
Y1 - 2022
N2 - Cardiomyocytes are contractile cells that regulate heart contraction. Ca2+ flux via Ca2+ channels activates actomyosin interactions, leading to cardiomyocyte contraction, which is modulated by physical factors (e.g., stretch, shear stress, and hydrostatic pressure). We evaluated the mechanism triggering slow contractions using a high-pressure microscope to characterize changes in cell morphology and intracellular Ca2+ concentration ([Ca2+]i) in mouse cardiomyocytes exposed to high hydrostatic pressures. We found that cardiomyocytes contracted slowly without an acute transient increase in [Ca2+]i, while a myosin ATPase inhibitor interrupted pressure-induced slow contractions. Furthermore, transmission electron microscopy showed that, although the sarcomere length was shortened upon the application of 20 MPa, this pressure did not collapse cellular structures such as the sarcolemma and sarcomeres. Our results suggest that pressure-induced slow contractions in cardiomyocytes are driven by the activation of actomyosin interactions without an acute transient increase in [Ca2+]i.
AB - Cardiomyocytes are contractile cells that regulate heart contraction. Ca2+ flux via Ca2+ channels activates actomyosin interactions, leading to cardiomyocyte contraction, which is modulated by physical factors (e.g., stretch, shear stress, and hydrostatic pressure). We evaluated the mechanism triggering slow contractions using a high-pressure microscope to characterize changes in cell morphology and intracellular Ca2+ concentration ([Ca2+]i) in mouse cardiomyocytes exposed to high hydrostatic pressures. We found that cardiomyocytes contracted slowly without an acute transient increase in [Ca2+]i, while a myosin ATPase inhibitor interrupted pressure-induced slow contractions. Furthermore, transmission electron microscopy showed that, although the sarcomere length was shortened upon the application of 20 MPa, this pressure did not collapse cellular structures such as the sarcolemma and sarcomeres. Our results suggest that pressure-induced slow contractions in cardiomyocytes are driven by the activation of actomyosin interactions without an acute transient increase in [Ca2+]i.
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U2 - 10.1016/j.bpj.2022.07.016
DO - 10.1016/j.bpj.2022.07.016
M3 - Article
C2 - 35841143
AN - SCOPUS:85135339209
SN - 0006-3495
JO - Biophysical Journal
JF - Biophysical Journal
ER -