TY - JOUR
T1 - The effects of load on transmural differences in contraction of isolated mouse ventricular cardiomyocytes
AU - Khokhlova, Anastasia
AU - Iribe, Gentaro
AU - Katsnelson, Leonid
AU - Naruse, Keiji
AU - Solovyova, Olga
N1 - Funding Information:
Wet experiments and simulations were supported by RF Government Resolution #211 of March 16, 2013 and JSPS KAKENHI #26282121, #16K12878. The development of mouse ventricular cardiomyocyte model was supported by the Russian Foundation for Basic Research (# 16-31-60015 ). The authors would like to thank Dr. Yohei Yamaguchi, Ms. Keiko Kaihara (Okayama University, Japan) and Dr. Toshiyuki Kaneko (Asahikawa Medical University, Japan) for to the valuable comments and advice.
Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2018/1
Y1 - 2018/1
N2 - Mechanical properties of cardiomyocytes from different transmural regions are heterogeneous in the left ventricular wall. The cardiomyocyte mechanical environment affects this heterogeneity because of mechano-electric feedback mechanisms. In the present study, we investigated the effects of the mechanical load (preload and afterload) on transmural differences in contraction of subendocardial (ENDO) and subepicardial (EPI) single cells isolated from the murine left ventricle. Various preloads imposed via axial stretch and afterloads (unloaded and heavy loaded conditions) were applied to the cells using carbon fiber techniques for single myocytes. To simulate experimentally obtained results and to predict mechanisms underlying the cellular response to change in load, our mathematical models of the ENDO and EPI cells were used. Our major findings are the following. Our results show that ENDO and EPI cardiomyocytes have different mechanical responses to changes in preload to the cells. Under auxotonic contractions at low preload (unstretched cells), time to peak contraction (T max ) and the time constant of [Ca 2 + ] i transient decay were significantly longer in ENDO cells than in EPI cells. An increase in preload (stretched cells) prolonged T max in both cell types; however, the prolongation was greater in EPI cells, resulting in a decrease in the transmural gradient in T max at high preload. Comparing unloaded and heavy loaded (isometric) contractions of the cells we found that transmural gradient in the time course of contraction is independent of the loading conditions. Our mathematical cell models were able to reproduce the experimental results on the distinct cellular responses to changes in the mechanical load when we accounted for an ENDO/EPI difference in the parameters of cooperativity of calcium activation of myofilaments.
AB - Mechanical properties of cardiomyocytes from different transmural regions are heterogeneous in the left ventricular wall. The cardiomyocyte mechanical environment affects this heterogeneity because of mechano-electric feedback mechanisms. In the present study, we investigated the effects of the mechanical load (preload and afterload) on transmural differences in contraction of subendocardial (ENDO) and subepicardial (EPI) single cells isolated from the murine left ventricle. Various preloads imposed via axial stretch and afterloads (unloaded and heavy loaded conditions) were applied to the cells using carbon fiber techniques for single myocytes. To simulate experimentally obtained results and to predict mechanisms underlying the cellular response to change in load, our mathematical models of the ENDO and EPI cells were used. Our major findings are the following. Our results show that ENDO and EPI cardiomyocytes have different mechanical responses to changes in preload to the cells. Under auxotonic contractions at low preload (unstretched cells), time to peak contraction (T max ) and the time constant of [Ca 2 + ] i transient decay were significantly longer in ENDO cells than in EPI cells. An increase in preload (stretched cells) prolonged T max in both cell types; however, the prolongation was greater in EPI cells, resulting in a decrease in the transmural gradient in T max at high preload. Comparing unloaded and heavy loaded (isometric) contractions of the cells we found that transmural gradient in the time course of contraction is independent of the loading conditions. Our mathematical cell models were able to reproduce the experimental results on the distinct cellular responses to changes in the mechanical load when we accounted for an ENDO/EPI difference in the parameters of cooperativity of calcium activation of myofilaments.
KW - Calcium transient
KW - Cellular mechanics
KW - Load dependency
KW - Mechano-calcium feedback
KW - Ventricular transmural heterogeneity
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U2 - 10.1016/j.yjmcc.2017.12.001
DO - 10.1016/j.yjmcc.2017.12.001
M3 - Article
C2 - 29217431
AN - SCOPUS:85037614859
SN - 0022-2828
VL - 114
SP - 276
EP - 287
JO - Journal of Molecular and Cellular Cardiology
JF - Journal of Molecular and Cellular Cardiology
ER -