Genetically engineered cardiac pacemaker: Stem cells transfected with HCN2 gene and myocytes - A model

被引:1
|
作者
Kanani, S. [1 ,2 ,5 ]
Pumir, A. [1 ,3 ,4 ,5 ]
Krinsky, V. [1 ,5 ]
机构
[1] CNRS, Inst Non Linear Nice, F-06560 Valbonne, France
[2] Inst Genom Fonct, F-34396 Montpellier, France
[3] Univ Nice, F-06108 Nice, France
[4] CNRS, Lab JA Dieudonne, F-06108 Nice, France
[5] Univ Nice, F-06560 Valbonne, France
关键词
biological pacemaker; gene therapy; oscillation; ion channels; stem cells;
D O I
10.1016/j.physleta.2007.07.075
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
One of the successfully tested methods to design genetically engineered cardiac pacemaker cells consists in transfecting a human mesenchymal stem cell (hMSC) with a HCN2 gene and connecting it to a myocyte. We develop and study a mathematical model, describing a myocyte connected to a hMSC transfected with a HCN2 gene. The cardiac action potential is described both with the simple Beeler-Reuter model, as well as with the elaborate dynamic Luo-Rudy model. The HCN2 channel is described by fitting electrophysiological records, in the spirit of Hodgkin-Huxley. The model shows that oscillations can occur in a pair myocyte-stem cell, that was not observed in the experiments yet. The model predicted that: (1) HCN pacemaker channels can induce oscillations only if the number of expressed IK1 channels is low enough. At too high an expression level of IK1 channels, oscillations cannot be induced, no matter how many pacemaker channels are expressed. (2) At low expression levels of IK1 channels, a large domain of values in the parameter space (n, N) exists, where oscillations should be observed. We denote N the number of expressed pacemaker channels in the stem cell, and n the number of gap junction channels coupling the stem cell and the myocyte. (3) The expression levels of IK1 channels observed in ventricular myocytes, both in the Beeler-Reuter and in the dynamic Luo-Rudy models are too high to allow to observe oscillations. With expression levels below similar to 4/4 of the original value, oscillations can be observed. The main consequence of this work is that in order to obtain oscillations in an experiment with a myocyte-stem cell pair, increasing the values of n, N is unlikely to be helpful, unless the expression level Of IK1 has been reduced enough. The model also allows us to explore levels of gene expression not yet achieved in experiments, and could be useful to plan new experiments, aimed at improving the robustness of the oscillations. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:141 / 147
页数:7
相关论文
共 50 条
  • [1] Genetically-engineered mesenchymal stem cells transfected with human HCN1 gene to create cardiac pacemaker cells
    Zhou, Ya-Feng
    Yang, Xiang-Jun
    Li, Hong-Xia
    Han, Lian-Huan
    Jiang, Wen-Ping
    JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2013, 41 (05) : 1570 - 1576
  • [2] Mesenchymal stem cells transfected with HCN2 genes by LentiV can be modified to be cardiac pacemaker cells
    Zhou, Ya-Feng
    Yang, Xiang-Jun
    Li, Hong-Xia
    Han, Lian-Huan
    Jiang, Wen-Ping
    MEDICAL HYPOTHESES, 2007, 69 (05) : 1093 - 1097
  • [3] Human mesenchymal stem cells transfected with HCN2 as a gene delivery system to induce pacemaker function in canine heart
    Plotnikov, AN
    Shlapakova, IN
    Danilo, P
    Herron, A
    Potapova, I
    Lu, ZG
    Doronin, S
    Brink, PR
    Robinson, RB
    Cohen, IS
    Rosen, MR
    CIRCULATION, 2003, 108 (17) : 547 - 547
  • [4] Associated changes in HCN2 and HCN4 transcripts and If pacemaker current in myocytes
    Zhang, Qi
    Huang, Aijie
    Lin, Yen-Chang
    Yu, Han-Gang
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2009, 1788 (05): : 1138 - 1147
  • [5] GENETICALLY ENGINEERED MESENCHYMAL STEM CELLS TO CREATE CARDIAC PACEMAKER CELLS
    Zhou, Ya-feng
    Yang, Xiang-jun
    Li, Hong-xia
    Han, Lian-hua
    Jiang, Wen-ping
    HEART, 2011, 97
  • [6] Mesenchymal stem cells genetically engineered to create cardiac pacemaker cells
    Zhou, Yafeng
    Yang, Xiangjun
    Li, Hongxia
    CIRCULATION, 2012, 125 (19) : E716 - E717
  • [7] The human gene coding for HCN2, a pacemaker channel of the heart
    Vaccari, T
    Moroni, A
    Rocchi, M
    Gorza, L
    Bianchi, ME
    Beltrame, M
    DiFrancesco, D
    BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1999, 1446 (03): : 419 - 425
  • [8] A novel HCN2 subunit modulates cardiac and thalamic pacemaker currents
    Silbernagel, N.
    Walecki, M.
    Schaefer, M.
    Kessler, M.
    Wemhoener, K.
    Zobeiri, M.
    Fortmueller, L.
    Scekic-Zahirovic, J.
    Rinne, S.
    Netter, M. F.
    Monassier, L.
    Just, S.
    Dupuis, L.
    Fabritz, L.
    Budde, T.
    Decher, N.
    ACTA PHYSIOLOGICA, 2015, 213 : 56 - 56
  • [9] MiRP1 modulates the HCN2 channel expression in cardiac myocytes
    Qu, JH
    Larsen, M
    Cohen, IS
    Robinson, RB
    BIOPHYSICAL JOURNAL, 2003, 84 (02) : 16A - 16A
  • [10] MiRP1 modulates HCN2 channel expression and gating in cardiac myocytes
    Qu, JH
    Kryukova, Y
    Potapova, IA
    Doronin, SV
    Larsen, M
    Krishnamurthy, G
    Cohen, IS
    Robinson, RB
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (42) : 43497 - 43502