4.5 Article

Cardiomyocyte sensor responsive to changes in physical and chemical environments

期刊

JOURNAL OF BIOMECHANICS
卷 47, 期 2, 页码 400-409

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jbiomech.2013.11.013

关键词

Cardiomyocyte sensor; Cardiac contraction force; PDMS cantilever

资金

  1. Program of the Korea Institute of Science and Technology (KIST) [2E24057]
  2. Pioneer Research Center Program through the National Research Foundation of Korea funded by the Ministry of Science
  3. ICT & Future Planning [NRF-2010-0019347]
  4. Korea Research Council of Fundamental Science 82 Technology [NAP-09-04]
  5. Basic Research Program through the National Research Foundation of Korea (NRF) [2012R1A5A2051387, 20110013333]
  6. Korea government (MEST)
  7. National Agenda Project (NAP)
  8. Ministry of Science
  9. National Research Council of Science & Technology (NST), Republic of Korea [NAP-09-4-KIST, 2E24120] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  10. National Research Foundation of Korea [2012R1A5A2051387, 2010-0019347, 2012R1A5A2048310] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Conventional cardiac physiology experiments investigate in vitro beat frequency using cells isolated from adult or neonatal rat hearts. In this study, we show that various cantilever shapes and drug treatments alter cardiomyocyte contraction force in vitro. Four types of cantilevers were used to compare the contractile forces: flat, peg patterned, grooved, and peg and grooved. Contraction force was represented as bending deflection of the cantilever end. The deflections of the flat, peg patterned, grooved, and peg and grooved cantilevers were 24.2 nN, 41.6 nN, 121 nN, and 134.2 nN, respectively. We quantified the effect of drug treatments on cardiomyocyte contractile forces on the grooved cantilever using Digoxin, Isoproterenol, and BayK8644, all of which increase contractile force, and Verapamil, which decreases contractile force. The cardiomyocyte contractile force without drugs decreased 8 days after culture initiation. Thus, we applied Digoxin, Isoproterenol, and BayK8644 at day 8, and Verapamil at day 5. Digoxin, Isoproterenol, and BayK8644 increased the cardiomyocyte contractile forces by 19.31%, 9.75%, and 23.81%, respectively. Verapamil decreased the contraction force by 48.06%. In summary, contraction force changes in response to adhesion surface topology and various types of drug treatments. We observed these changes by monitoring cell alignment, adhesion, morphology, and bending displacement with cantilever sensors. (C) 2013 Elsevier Ltd. All rights reserved.

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