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. Author manuscript; available in PMC: 2009 Mar 11.
Published in final edited form as: Am J Physiol Cell Physiol. 2006 Oct 25;292(3):C1156–C1166. doi: 10.1152/ajpcell.00397.2006

Fig. 4.

Fig. 4

ΔF/F (where F is fluorescence) line scan images from intact dedifferentiating adult mouse muscle fibers. Above each ΔF/F image is the mean temporal profile centered at the peak ΔF/F. These records represent a sampling of the various different time courses of local Ca2+ release events recorded from dedifferentiating fibers using line scan imaging. A, B, and F: line scan images and time courses of both rapidly rising and decaying fluorescence signals. Note that these signals are quite similar to Ca2+ sparks observed in frog and mammalian myofibers. C, D, and E: line scan images and time courses of slower rising and decaying events. Note that these records are similar to Ca2+ signals as seen in developing mammalian myofibers.

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