| High resolution measurement of striation patterns and sarcomere motions in cardiac muscle cells Biophysical Journal, Volume 61, Issue 1, 1 January 1992, Pages 129-144 J.W. Krueger and A. Denton Abstract We describe an extension of the method of Myers et al. (1982) to measure with high precision the uniformity of contractile motions that occur between sarcomeres in the isolated cardiac muscle cell (guinea pig and rat). The image of the striations, observed with modulation contrast microscopy, was detected by a linear array of photodiodes. Sarcomere length was measured greater than 500/s from the frequency of the array's video signal at two selectable regions of the cell. A precision test grating demonstrated that method resolves known differences in the spacing between two contiguous striations to +/- 0.01 micron and that the effects of image translation and microscopic resolution are minor. The distribution of striation spacing appears to be discrete in isolated segments of the cell, and patches of fairly uniform length can be identified that are laterally contiguous. When electrically triggered, contraction is synchronous and the sarcomeres shorten and relengthen smoothly. The contrast between the striations is transiently enhanced during relengthening, an indication that the contracting cell can not be treated as a simple grating. Pauses that occur during late in relengthening (and transient contractile alternans) are characterized by very synchronized activity. These forms of irregular contractile behavior are not explained by desynchronization of a mechanism of release of intracellular calcium. A companion article describes application of the technique to study the nonuniform motions that occur between sarcomeres. Abstract | PDF (3315 kb) |
| Sarcomere length uniformity determined from three-dimensional reconstructions of resting isolated heart cell striation patterns Biophysical Journal, Volume 52, Issue 2, 1 August 1987, Pages 317-327 K.P. Roos Abstract A- and I-band striation positions have been obtained, three-dimensionally reconstructed, and statistically analyzed from the volumes of resting isolated heart cells. Striation patterns from optically discrete subvolumes are imaged along the length of these myocytes with a computer-interfaced optical microscope imaging system. Planar striation maps are reconstructed by the computer from sequentially obtained striation pattern images displaced across the width or depth of the cell in controlled steps. Multiple planar maps are combined to form full three-dimensional (3-D) reconstructions that illustrate the sarcomeric structure and ordering throughout the volume of the cell. These reconstructions demonstrate a high degree of striation registration throughout most regions of cardiac cells. The striation registration is often slightly (less than 10 degrees) skewed across the width or depth of nearly every cell and is occasionally disrupted between adjacent groups of sarcomeres. These disruptions in registration are always associated with the locations of the nuclei. Rigorous statistical analyses indicate small volumetric regions of the cell delineated by these disruptions can have significantly (0.014–0.113 micron) shorter or longer average sarcomere length periodicities. Unlike skeletal muscle "fibrillenstruktur," these data from cardiac cells exhibit no evidence of helical packing schemes for sarcomere order. These observations suggest that the relatively large nuclei displace and disrupt the normal registration of the sarcomeres, which is probably mediated by internal cytoskeletal structures. Abstract | PDF (1868 kb) |
| Localization and Kinetics of Protein Kinase C-Epsilon Anchoring in Cardiac Myocytes Biophysical Journal, Volume 80, Issue 5, 1 May 2001, Pages 2140-2151 Seth L. Robia, Jyothi Ghanta, Valentin G. Robu and Jeffery W. Walker Abstract Protein kinase C- (PKC-) plays a central role in cardiac cell signaling, but mechanisms of translocation and anchoring upon activation are poorly understood. Conventional PKC isoforms rely on a rapid Ca-mediated recruitment to cell membranes, but this mechanism cannot be employed by PKC- or other PKC isoforms lacking a Ca-binding domain. In this study, we used recombinant green fluorescent protein (GFP) fusion constructs and confocal microscopy to examine the localization, kinetics, and reversibility of PKC- anchoring in permeabilized rat cardiac myocytes. PKC--GFP bound with a striated pattern that co-localized with -actinin, a marker of the Z-line of the sarcomere. Binding required activation of PKC and occurred slowly but reversibly with apparent rate constants of =4.6±1.2×10M s and =1.4±0.5×10 s (=8min) as determined by fluorescence recovery after photobleaching and by perfusion experiments. A truncated construct composed of the N-terminal 144-amino-acid variable region of PKC- (V-GFP), but not an analogous N-terminal domain of PKC-, mimicked the Z-line decoration and slow binding rate of the full-length enzyme. These findings suggest that the V domain is important in determining PKC- localization and translocation kinetics in cardiac muscle. Moreover, PKC- translocation is not a diffusion-controlled binding process but instead may be limited by intramolecular conformational changes within the V domain. The for V-GFP was two- to threefold faster than for full-length enzyme, indicating that other domains in PKC- contribute to anchoring by prolonging the bound state. Abstract | Full Text | PDF (1454 kb) |
Copyright © 1982 The Biophysical Society. All rights reserved.
Biophysical Journal, Volume 40, Issue 3, 233-244, 1 December 1982
doi:10.1016/S0006-3495(82)84478-0
Research Article
K.P. Roos and A.J. Brady
Discrete sarcomere lengths have been determined from dynamically contracting isolated cardiac cells with a high-speed, high-resolution direct optical imaging system. Calcium-tolerant cardiac cells from the rat are isolated by perfusion with collagenase and hyaluronidase. Individual sarcomere lengths can be determined by directly imaging the cell's striation pattern onto a solid-state charge-coupled device (CCD) detector interfaced with a digital computer. The precision of detection in a real light microscopic optical system is discussed in relation to the type of image detector, optical contract enhancement techniques, and digital image processing. The optical performance of the direct striation pattern image apparatus has been determined empirically with test grids under standard bright-field and Nomarski-differential interference contrast (DIC) conditions for application to real muscle imaging. Discrete striation positions of isolated cells have been detected and followed with high precision during phasic contraction-relaxation cycles down to average sarcomere lengths as short as 1.43 +/- 0.053 microns. The maximum rates of contraction and relaxation are rapid and synchronous in time course along the length of the cell. These results indicate that direct optical imaging can provide an accurate means to monitor discrete striations and sarcomere lengths along the length of Ca2+-tolerant heart cells.