4.6 Article

Contractile properties of developing human fetal cardiac muscle

期刊

JOURNAL OF PHYSIOLOGY-LONDON
卷 594, 期 2, 页码 437-452

出版社

WILEY
DOI: 10.1113/JP271290

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资金

  1. NIH from the Eunice Kennedy Shriver National Institute of Child Health & Human Development [5R24HD0008836]
  2. NIH [P30 EY01730, HL65497, HL11197, HD048895, HD057331, F31AR063000]
  3. Heart and Stroke Foundation of Canada Postdoctoral Fellowship

向作者/读者索取更多资源

Little is known about the contractile properties of human fetal cardiac muscle during development. Understanding these contractile properties, and how they change throughout development, can provide valuable insight into human heart development, and provide a framework to study the early stages of cardiac diseases that develop in utero. We characterized the contractile properties of isolated human fetal cardiac myofibrils across 8-19 weeks of gestation. Mechanical measurements revealed that in early stages of gestation there is low specific force and slow rates of force development and relaxation, with increases in force and the rates of activation and relaxation as gestation progresses. The duration and slope of the initial, slow phase of relaxation, related to myosin detachment and thin filament deactivation rates, decreased with gestation age. F-actin sliding on human fetal cardiac myosin-coated surfaces slowed significantly from 108 to 130 days of gestation. Electron micrographs showed human fetal muscle myofibrils elongate and widen with age, but features such as the M-line and Z-band are apparent even as early as day 52. Protein isoform analysis revealed that -myosin is predominantly expressed even at the earliest time point studied, but there is a progressive increase in expression of cardiac troponin I (TnI), with a concurrent decrease in slow skeletal TnI. Together, our results suggest that cardiac myofibril force production and kinetics of activation and relaxation change significantly with gestation age and are influenced by the structural maturation of the sarcomere and changes in contractile filament protein isoforms.

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