PACEMAKER ACTIVITY AND MITOSIS IN CULTURES OF NEWBORN RAT HEART VENTRICLE CELLS
PACEMAKER ACTIVITY AND MITOSIS IN CULTURES OF NEWBORN RAT HEART VENTRICLE CELLS
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DOI:
10.1016/0014-4827(66)90427-7
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发表时间:
1966-01-01
影响因子:
3.7
通讯作者:
STRASSER, FF
中科院分区:
文献类型:
--
作者:
MARK, GE;STRASSER, FF
A reproducible culture system was described in which single newborn rat heart ventricle cells develop into a differentiated, synchronously-beating network and continue to function for many weeks with no evidence of dedifferentiation and no loss of beating rate. Contrary to the accepted idea that only the "pacemaker" cells of the heart may initiate beating, results indicate that all muscle cells in the newborn rat heart ventricle appear to be capable of independent and spontaneous contraction of tissue culture. The rate of beating varies widely from cell to cell. The significance of this in relation to embryological development of the heart was discussed. Groups of connected muscle cells contract in synchrony, the fastest beating cell acting as pacemaker. The protoplasmic connection necessary for synchronization of beating need not be directly from one muscle cell to another, but may be made through the non-muscle cells, probably of endothelial origin. Synchronization upon cell contact (as defined by high resolution phase microscopy) is rapid but not instantaneous. Heart muscle cells may undergo mitosis while continuing to beat. The mitosis appears to be modified to assure the continued function of the cell as part of a tissue unit during this process. A double membrane surrounding the nucleus of all heart muscle cells, and clearly visible with the phase microscope, was observed.