Paper
22 February 2012 Live cardiomyocyte imaging via hybrid TPEF-SHG microscopy
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Abstract
Utilizing a custom-built, on-stage incubator-combined, two-photon excitation fluorescence (TPEF) and second harmonic generation (SHG) imaging system, we observed new-sarcomere addition in rat neonatal cardiomyocytes during 10 hours of on-stage incubation. This addition occurred at one end of an existing myofibril, the sides of existing myofibrils, and at the interstice of several separated myofibrils; in the cases of the latter two, we observed mature myofibrils acting as templates. We found that during sarcomeric addition, myosin filaments are assembled onto the premyofibril laterally. This lateral addition, which proceeds stepwise along the axial direction, plays an important role in the accumulation of Z-bodies to form mature Z-disks and in the regulation of sarcomeric length during maturation.
© (2012) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Honghai Liu, Wan Qin, Yonghong Shao, Qiuying Liu, Zhen Ma, Thomas K. Borg, and Bruce Z. Gao "Live cardiomyocyte imaging via hybrid TPEF-SHG microscopy", Proc. SPIE 8225, Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues X, 822524 (22 February 2012); https://doi.org/10.1117/12.908381
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Cited by 3 scholarly publications.
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KEYWORDS
Second-harmonic generation

Imaging systems

Proteins

Femtosecond phenomena

Harmonic generation

Luminescence

Microscopy

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