Nanoscopic changes in the lattice structure of striated muscle sarcomeres involved in the mechanism of spontaneous oscillatory contraction (SPOC)

被引:10
|
作者
Kono, Fumiaki [1 ,2 ]
Kawai, Seitaro [1 ]
Shimamoto, Yuta [3 ]
Ishiwata, Shin'ichi [1 ]
机构
[1] Waseda Univ, Dept Phys, Fac Sci & Engn, Shinjuku Ku, 3-4-1 Okubo, Tokyo 1698555, Japan
[2] Natl Inst Quantum & Radiol Sci & Technol, Inst Quantum Life Sci, 2-4 Shirakata, Tokai, Ibaraki 3191106, Japan
[3] Natl Inst Genet, Dept Chromosome Sci, Lab Phys & Cell Biol, 1111 Yata, Mishima, Shizuoka 4118540, Japan
关键词
SPONTANEOUS TENSION OSCILLATION; LENGTH-DEPENDENT ACTIVATION; FRANK-STARLING MECHANISM; SINGLE-SKINNED FIBERS; X-RAY-DIFFRACTION; SKELETAL MYOFIBRILS; SELECTIVE DIGESTION; ELASTIC FILAMENTS; ACTIN-FILAMENT; THIN-FILAMENTS;
D O I
10.1038/s41598-020-73247-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Muscles perform a wide range of motile functions in animals. Among various types are skeletal and cardiac muscles, which exhibit a steady auto-oscillation of force and length when they are activated at an intermediate level of contraction. This phenomenon, termed spontaneous oscillatory contraction or SPOC, occurs devoid of cell membranes and at fixed concentrations of chemical substances, and is thus the property of the contractile system per se. We have previously developed a theoretical model of SPOC and proposed that the oscillation emerges from a dynamic force balance along both the longitudinal and lateral axes of sarcomeres, the contractile units of the striated muscle. Here, we experimentally tested this hypothesis by developing an imaging-based analysis that facilitates detection of the structural changes of single sarcomeres at unprecedented spatial resolution. We found that the sarcomere width oscillates anti-phase with the sarcomere length in SPOC. We also found that the oscillatory dynamics can be altered by osmotic compression of the myofilament lattice structure of sarcomeres, but they are unchanged by a proteolytic digestion of titin/connectin-the spring-like protein that provides passive elasticity to sarcomeres. Our data thus reveal the three-dimensional mechanical dynamics of oscillating sarcomeres and suggest a structural requirement of steady auto-oscillation.
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页数:14
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