Organization of connectin/titin filaments in sarcomeres of differentiating chicken skeletal muscle cells |
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Authors: | Yoshinori Soeno Hirohiko Yajima Yuuki Kawamura Sumiko Kimura Koscak Maruyama Takashi Obinata |
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Affiliation: | (1) Department of Biology, Faculty of Science, Chiba University, Chiba, Japan |
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Abstract: | Very long, elastic connectin/titin molecules position the myosin filaments at the center of a sarcomere by linking them to the Z line. The behavior of the connectin filaments during sarcomere formation in differentiating chicken skeletal muscle cells was observed under a fluorescent microscope using the antibodies to the N terminal (located in the Z line), C terminal (M line), and C zone (myosin filament) regions of connectin and was compared to the incorporation of -actinin and myosin into forming sarcomeres. In early stages of differentiating muscle cells, the N terminal region of connectin was incorporated into a stress fiber-like structure (SFLS) together with -actinin to form dots, whereas the C terminal region was diffusely distributed in the cytoplasm. When both the C and N terminal regions formed striations in young myofibrils, the epitope to the C zone of A-band region, that is the center between the A-I junction and the M-line, initially was diffuse in appearance and later formed definite striations. It appears that it took some time for the N and C terminal regions of connectin to form a regular organization in a sarcomere. Thus the two ends of the connectin filaments were first fixed followed by the specific binding of the middle portion onto the myosin filament during sarcomere formation. |
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Keywords: | connectin/titin /content/v45791682u122121/xxlarge945.gif" alt=" agr" align=" BASELINE" BORDER=" 0" >-actinin myosin sarcomere formation chicken skeletal muscle |
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