Myofibrillogenesis in the first cardiomyocytes formed from isolated quail precardiac mesoderm.

De novo assembly of myofibrils was investigated in explants of precardiac mesoderm from quail embryos to address a controversy about different models of myofibrillogenesis. The sequential expression of sarcomeric components was visualized in double- and triple-stained explants before, during, and just after the first cardiomyocytes began to beat. In explants from stage 6 embryos, cultured for 10 h, ectoderm, endoderm, and the precardiac mesoderm displayed arrays of stress fibers with alternating bands of the nonmuscle isoforms of alpha-actinin and myosin IIB. With increasing time in culture, mesoderm cells contained fibrils composed of actin, nonmuscle myosin IIB, and sarcomeric alpha-actinin. Several hours later, before beating occurred, both nonmuscle and muscle myosin II localized in some of the fibrils in the cells. Concentrations of muscle myosin began as thin bundles, dispersed in the cytoplasm, often overlapping one another, and progressed to small, aligned A-band-sized aggregates. The amount of nonmuscle myosin decreased dramatically when Z-bands formed, the muscle myosin became organized into A-bands, and the cells began beating. The sequential changes in protein composition of the fibrils in the developing muscle cells supports the model of myofibrillogenesis in which assembly begins with premyofibrils and progresses through nascent myofibrils to mature myofibrils.

[1]  J. Sanger,et al.  Myofibrillogenesis in Cardiac Muscle , 2002 .

[2]  S. Kawamoto,et al.  Cloning of the cDNA encoding the myosin heavy chain of a vertebrate cellular myosin. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[3]  M. Yanagisawa,et al.  Two distinct nonmuscle myosin-heavy-chain mRNAs are differentially expressed in various chicken tissues. Identification of a novel gene family of vertebrate non-sarcomeric myosin heavy chains. , 1989, European journal of biochemistry.

[4]  S. Kawamoto,et al.  Chicken nonmuscle myosin heavy chains: differential expression of two mRNAs and evidence for two different polypeptides , 1991, The Journal of cell biology.

[5]  J C Perriard,et al.  Myofibrillogenesis in the developing chicken heart: assembly of Z-disk, M-line and the thick filaments. , 1999, Journal of cell science.

[6]  C. Gregorio,et al.  To the heart of myofibril assembly. , 2000, Trends in cell biology.

[7]  N. Spitzer,et al.  A Calcium Signaling Cascade Essential for Myosin Thick Filament Assembly in Xenopus Myocytes , 1998, The Journal of cell biology.

[8]  J. Sanger,et al.  The premyofibril: evidence for its role in myofibrillogenesis. , 1994, Cell motility and the cytoskeleton.

[9]  K. Linask,et al.  N-cadherin is required for the differentiation and initial myofibrillogenesis of chick cardiomyocytes. , 1998, Cell motility and the cytoskeleton.

[10]  Nathan Christopher Shaner,et al.  Myofibrillogenesis in skeletal muscle cells. , 2002, Clinical orthopaedics and related research.

[11]  K. Burridge,et al.  Focal adhesions, contractility, and signaling. , 1996, Annual review of cell and developmental biology.

[12]  Viktor Hamburger,et al.  A series of normal stages in the development of the chick embryo , 1992, Journal of morphology.

[13]  Y. Shimada,et al.  Dynamics of Actin and α-Actinin in Nascent Myofibrils and Stress Fibers , 2004, Journal of Muscle Research & Cell Motility.

[14]  J. C. Ayoob,et al.  Assembly of myofibrils in cardiac muscle cells. , 2000, Advances in experimental medicine and biology.

[15]  J. Sanger,et al.  Banding and polarity of actin filaments in interphase and cleaving cells , 1980, The Journal of cell biology.

[16]  K. Linask,et al.  Early heart development: Dynamics of endocardial cell sorting suggests a common origin with cardiomyocytes , 1993, Developmental dynamics : an official publication of the American Association of Anatomists.

[17]  J. Sanger,et al.  Myofibrillogenesis visualized in living embryonic cardiomyocytes. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[18]  J. Sanger,et al.  Amorphin is phosphorylase; phosphorylase is an alpha-actinin-binding protein. , 2002, Cell motility and the cytoskeleton.

[19]  J. Murray,et al.  The vinculin/sarcomeric-alpha-actinin/alpha-actin nexus in cultured cardiac myocytes , 1992, The Journal of cell biology.

[20]  V. Hamburger,et al.  A series of normal stages in the development of the chick embryo. 1951. , 2012, Developmental dynamics : an official publication of the American Association of Anatomists.

[21]  J. Sanger,et al.  Observations of Microfilament Bundles in Living Cells Microinjected with Fluorescently Labelled Contractile Proteins , 1986, Journal of Cell Science.

[22]  S. Kawamoto,et al.  Human nonmuscle myosin heavy chains are encoded by two genes located on different chromosomes. , 1991, Circulation research.

[23]  G. Conrad,et al.  Subcellular compartmentalization of myosin isoforms in embryonic chick heart ventricle myocytes during cytokinesis. , 1991, Cell motility and the cytoskeleton.

[24]  J. C. Ayoob,et al.  Targeting of cardiac muscle titin fragments to the Z-bands and dense bodies of living muscle and non-muscle cells. , 2000, Cell motility and the cytoskeleton.

[25]  J. Dome,et al.  Analysis of cell division using fluorescently labeled actin and myosin in living PtK2 cells. , 1989, Cell motility and the cytoskeleton.

[26]  H. Hidaka,et al.  Selective inhibition of catalytic activity of smooth muscle myosin light chain kinase. , 1987, The Journal of biological chemistry.

[27]  F. Protasi,et al.  Independent assembly of 1.6 microns long bipolar MHC filaments and I-Z-I bodies. , 1997, Cell structure and function.

[28]  J. C. Ayoob,et al.  Transfections of primary muscle cell cultures with plasmids coding for GFP linked to full-length and truncated muscle proteins. , 1999, Methods in cell biology.

[29]  J. Kolega,et al.  Asymmetry in the distribution of free versus cytoskeletal myosin II in locomoting microcapillary endothelial cells. , 1997, Experimental cell research.

[30]  M. Elzinga,et al.  Studies on the distribution of cellular myosin with antibodies to isoform‐specific synthetic peptides , 1991, FEBS letters.

[31]  S. M. Wang,et al.  Studies on cardiac myofibrillogenesis with antibodies to titin, actin, tropomyosin, and myosin , 1988, The Journal of cell biology.

[32]  J. Sanger,et al.  Formation of myofibrils in spreading chick cardiac myocytes. , 1984, Cell motility.

[33]  J. Sanger,et al.  Premyofibrils in spreading adult cardiomyocytes in tissue culture: evidence for reexpression of the embryonic program for myofibrillogenesis in adult cells. , 1997, Cell motility and the cytoskeleton.

[34]  G. Conrad,et al.  Differential localization of cytoplasmic myosin II isoforms A and B in avian interphase and dividing embryonic and immortalized cardiomyocytes and other cell types in vitro. , 1995, Cell motility and the cytoskeleton.

[35]  K. Yamada,et al.  Synthetic peptides that mimic the adhesive recognition signal of fibronectin: differential effects on cell-cell and cell-substratum adhesion in embryonic chick cells. , 1987, Developmental biology.

[36]  J. Sanger Green Fluorescent Proteins Improve Myofibril Research , 2001 .

[37]  T. Yatskievych,et al.  Assembly of thick, thin, and titin filaments in chick precardiac explants , 2001, Developmental dynamics : an official publication of the American Association of Anatomists.

[38]  J. Sanger,et al.  Fishing out proteins that bind to titin , 2001, The Journal of cell biology.

[39]  J. C. Ayoob,et al.  Use of green fluorescent proteins linked to cytoskeletal proteins to analyze myofibrillogenesis in living cells. , 1999, Methods in enzymology.

[40]  U. K. Laemmli,et al.  Cleavage of structural proteins during , 1970 .

[41]  J. Sanger,et al.  Myofibrillogenesis in living cells microinjected with fluorescently labeled alpha-actinin , 1986, The Journal of cell biology.

[42]  S. M. Wang,et al.  N‐cadherin/catenin–based costameres in cultured chicken cardiomyocytes , 1999, Journal of cellular biochemistry.