Strategies to Study Desmin in Cardiac Muscle and Culture Systems

Bar, 2007, Conspicuous involvement of desmin tail mutations in diverse cardiac and skeletal myopathies, Human Mutation, 28, 374, 10.1002/humu.20459 Bar, 2006, Forced expression of desmin and desmin mutants in cultured cells: Impact of myopathic missense mutations in the central coiled-coil domain on network formation, Experimental Cell Research, 312, 1554, 10.1016/j.yexcr.2006.01.021 Bar, 2007, Assembly defects of desmin disease mutants carrying deletions in the alpha-helical rod domain are rescued by wild type protein, Journal of Structural Biology, 158, 107, 10.1016/j.jsb.2006.10.029 Bar, 2005, Severe muscle disease-causing desmin mutations interfere with in vitro filament assembly at distinct stages, Proceedings of the National Academy of Sciences of the United States of America, 102, 15099, 10.1073/pnas.0504568102 Bar, 2004, The biology of desmin filaments: How do mutations affect their structure, assembly, and organisation?, Journal of Structural Biology, 148, 137, 10.1016/j.jsb.2004.04.003 Blau, 1983, Cytoplasmic activation of human nuclear genes in stable heterocaryons, Cell, 32, 1171, 10.1016/0092-8674(83)90300-8 Capetanaki, 2007, Muscle intermediate filaments and their links to membranes and membranous organelles, Experimental Cell Research, 313, 2063, 10.1016/j.yexcr.2007.03.033 Capetanaki, 2015, Desmin related disease: A matter of cell survival failure, Current Opinion in Cell Biology, 32C, 113, 10.1016/j.ceb.2015.01.004 Capetanaki, 1989, Overexpression of the vimentin gene in transgenic mice inhibits normal lens cell differentiation, The Journal of Cell Biology, 109, 1653, 10.1083/jcb.109.4.1653 Claycomb, 1998, HL-1 cells: A cardiac muscle cell line that contracts and retains phenotypic characteristics of the adult cardiomyocyte, Proceedings of the National Academy of Sciences of the United States of America, 95, 2979, 10.1073/pnas.95.6.2979 Clemen, 2015, The toxic effect of R350P mutant desmin in striated muscle of man and mouse, Acta Neuropathologica, 129, 297, 10.1007/s00401-014-1363-2 Doetschman, 1985, The in vitro development of blastocyst-derived embryonic stem cell lines: Formation of visceral yolk sac, blood islands and myocardium, Journal of Embryology and Experimental Morphology, 87, 27 Fire, 1990, A modular set of lacZ fusion vectors for studying gene expression in Caenorhabditis elegans, Gene, 93, 189, 10.1016/0378-1119(90)90224-F Frezza, 2007, Organelle isolation: Functional mitochondria from mouse liver, muscle and cultured fibroblasts, Nature Protocols, 2, 287, 10.1038/nprot.2006.478 Goodell, 1996, Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo, The Journal of Experimental Medicine, 183, 1797, 10.1084/jem.183.4.1797 Havaki, 2003, Ultrastructural immunostaining of infiltrating ductal breast carcinomas with the monoclonal antibody H: A comparative study with cytokeratin 8, Ultrastructural Pathology, 27, 393, 10.1080/01913120390209875 Herrmann, 2000, Intermediate filaments and their associates: Multi-talented structural elements specifying cytoarchitecture and cytodynamics, Current Opinion in Cell Biology, 12, 79, 10.1016/S0955-0674(99)00060-5 Herrmann, 2004, Isolation, characterization, and in vitro assembly of intermediate filaments, Methods in Cell Biology, 78, 3, 10.1016/S0091-679X(04)78001-2 Hofner, 2007, Desmin stimulates differentiation of cardiomyocytes and up-regulation of brachyury and nkx2.5, Differentiation, 75, 605, 10.1111/j.1432-0436.2007.00162.x Hollrigl, 2007, Differentiation of cardiomyocytes requires functional serine residues within the amino-terminal domain of desmin, Differentiation, 75, 616, 10.1111/j.1432-0436.2007.00163.x Ieda, 2010, Direct reprogramming of fibroblasts into functional cardiomyocytes by defined factors, Cell, 142, 375, 10.1016/j.cell.2010.07.002 Itskovitz-Eldor, 2000, Differentiation of human embryonic stem cells into embryoid bodies compromising the three embryonic germ layers, Molecular Medicine, 6, 88, 10.1007/BF03401776 Kettleborough, 2013, A systematic genome-wide analysis of zebrafish protein-coding gene function, Nature, 496, 494, 10.1038/nature11992 Kimes, 1976, Properties of a clonal muscle cell line from rat heart, Experimental Cell Research, 98, 367, 10.1016/0014-4827(76)90447-X Kostareva, 2008, Mice expressing L345P mutant desmin exhibit morphological and functional changes of skeletal and cardiac mitochondria, Journal of Muscle Research and Cell Motility, 29, 25, 10.1007/s10974-008-9139-8 Kouloumenta, 2007, Proper perinuclear localization of the TRIM-like protein myospryn requires its binding partner desmin, The Journal of Biological Chemistry, 282, 35211, 10.1074/jbc.M704733200 Kuisk, 1996, A single MEF2 site governs desmin transcription in both heart and skeletal muscle during mouse embryogenesis, Developmental Biology, 174, 1, 10.1006/dbio.1996.0046 Li, 2013, Knockdown of desmin in zebrafish larvae affects interfilament spacing and mechanical properties of skeletal muscle, The Journal of General Physiology, 141, 335, 10.1085/jgp.201210915 Li, 1994, Inhibition of desmin expression blocks myoblast fusion and interferes with the myogenic regulators MyoD and myogenin, The Journal of Cell Biology, 124, 827, 10.1083/jcb.124.5.827 Li, 1996, Cardiovascular lesions and skeletal myopathy in mice lacking desmin, Developmental Biology, 175, 362, 10.1006/dbio.1996.0122 Loh, 2000, Characterization of a zebrafish (Danio rerio) desmin cDNA: An early molecular marker of myogenesis, Differentiation, 65, 247, 10.1046/j.1432-0436.2000.6550247.x Macgregor, 1991, Use of Escherichia coli (E. coli) lacZ (beta-galactosidase) as a Reporter Gene, Methods in Molecular Biology, 7, 217 Mavroidis, 2002, Extensive induction of important mediators of fibrosis and dystrophic calcification in desmin-deficient cardiomyopathy, The American Journal of Pathology, 160, 943, 10.1016/S0002-9440(10)64916-4 Mavroidis, 2015, Complement system modulation as a target for treatment of arrhythmogenic cardiomyopathy, Basic Research in Cardiology, 110, 485, 10.1007/s00395-015-0485-6 Mavroidis, 2008, A missense mutation in desmin tail domain linked to human dilated cardiomyopathy promotes cleavage of the head domain and abolishes its Z-disc localization, The FASEB Journal, 22, 3318, 10.1096/fj.07-088724 McMahon, 1990, The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain, Cell, 62, 1073, 10.1016/0092-8674(90)90385-R Milner, 2000, Desmin cytoskeleton linked to muscle mitochondrial distribution and respiratory function, The Journal of Cell Biology, 150, 1283, 10.1083/jcb.150.6.1283 Milner, 1996, Disruption of muscle architecture and myocardial degeneration in mice lacking desmin, The Journal of Cell Biology, 134, 1255, 10.1083/jcb.134.5.1255 Nikolova, 2004, Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice, The Journal of Clinical Investigation, 113, 357, 10.1172/JCI200419448 Oyama, 2007, Cardiac side population cells have a potential to migrate and differentiate into cardiomyocytes in vitro and in vivo, The Journal of Cell Biology, 176, 329, 10.1083/jcb.200603014 Panagopoulou, 2008, Desmin mediates TNF-alpha-induced aggregate formation and intercalated disk reorganization in heart failure, Journal of Cell Biology, 181, 761, 10.1083/jcb.200710049 Papathanasiou, 2015, Tumor necrosis factor-alpha confers cardioprotection through ectopic expression of keratins K8 and K18, Nature Medicine, 21, 1076, 10.1038/nm.3925 Pfister, 2005, CD31− but not CD31+ cardiac side population cells exhibit functional cardiomyogenic differentiation, Circulation Research, 97, 52, 10.1161/01.RES.0000173297.53793.fa Pfister, 2010, Isolation of resident cardiac progenitor cells by Hoechst 33342 staining, Methods in Molecular Biology, 660, 53, 10.1007/978-1-60761-705-1_4 Psarras, 2012, Regulation of adverse remodelling by osteopontin in a genetic heart failure model, European Heart Journal, 33, 1954, 10.1093/eurheartj/ehr119 Qian, 2013, Reprogramming of mouse fibroblasts into cardiomyocyte-like cells in vitro, Nature Protocols, 8, 1204, 10.1038/nprot.2013.067 Qian, 2012, In vivo reprogramming of murine cardiac fibroblasts into induced cardiomyocytes, Nature, 485, 593, 10.1038/nature11044 Ralston, 2006, Blood vessels and desmin control the positioning of nuclei in skeletal muscle fibers, Journal of Cellular Physiology, 209, 874, 10.1002/jcp.20780 Ramspacher, 2015, Developmental alterations in heart biomechanics and skeletal muscle function in desmin mutants suggest an early pathological root for desminopathies, Cell Reports, 11, 1564, 10.1016/j.celrep.2015.05.010 Robertson, 1992, An appraisal of low-temperature embedding by progressive lowering of temperature into Lowicryl HM20 for immunocytochemical studies, Journal of Microscopy, 168, 85, 10.1111/j.1365-2818.1992.tb03253.x Robson, 2004, Muscle intermediate filament proteins, Methods in Cell Biology, 78, 519, 10.1016/S0091-679X(04)78018-8 Sarria, 1994, The presence or absence of a vimentin-type intermediate filament network affects the shape of the nucleus in human SW-13 cells, Journal of Cell Science, 107, 1593, 10.1242/jcs.107.6.1593 Sarria, 1990, Regulated expression of vimentin cDNA in cells in the presence and absence of a preexisting vimentin filament network, The Journal of Cell Biology, 111, 553, 10.1083/jcb.111.2.553 Schweitzer, 2001, Paranemin and the organization of desmin filament networks, Journal of Cell Science, 114, 1079, 10.1242/jcs.114.6.1079 Shah, 2004, Structural and functional roles of desmin in mouse skeletal muscle during passive deformation, Biophysical Journal, 86, 2993, 10.1016/S0006-3495(04)74349-0 Song, 2012, Heart repair by reprogramming non-myocytes with cardiac transcription factors, Nature, 485, 599, 10.1038/nature11139 Soriano, 1991, Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice, Cell, 64, 693, 10.1016/0092-8674(91)90499-O Thornell, 1997, Null mutation in the desmin gene gives rise to a cardiomyopathy, Journal of Molecular and Cellular Cardiology, 29, 2107, 10.1006/jmcc.1997.0446 Trinh le, 2011, A versatile gene trap to visualize and interrogate the function of the vertebrate proteome, Genes & Development, 25, 2306, 10.1101/gad.174037.111 Tsoupri, 2013, Muyospryn: A multifunctional desmin-associated protein, Histochemistry and Cell Biology, 140, 55, 10.1007/s00418-013-1103-z Vogel, 2009, In-vivo characterization of human dilated cardiomyopathy genes in zebrafish, Biochemical and Biophysical Research Communications, 390, 516, 10.1016/j.bbrc.2009.09.129 Vorgias, 1983, Isolation, purification and characterization of the intermediate filament protein desmin from porcine smooth muscle, Preparative Biochemistry, 13, 227, 10.1080/00327488308064250 Wang, 2001, Mouse model of desmin-related cardiomyopathy, Circulation, 103, 2402, 10.1161/01.CIR.103.19.2402 Weitzer, 1995, Cytoskeletal control of myogenesis: A desmin null mutation blocks the myogenic pathway during embryonic stem cell differentiation, Developmental Biology, 172, 422, 10.1006/dbio.1995.8070 Wieckowski, 2009, Isolation of mitochondria-associated membranes and mitochondria from animal tissues and cells, Nature Protocols, 4, 1582, 10.1038/nprot.2009.151 Yaffe, 1977, Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle, Nature, 270, 725, 10.1038/270725a0 Yuan, 1999, The effects of mono-ADP-ribosylation on desmin assembly-disassembly, Archives of Biochemistry and Biophysics, 363, 314, 10.1006/abbi.1998.1096 Zhou, 2000, Culture and adenoviral infection of adult mouse cardiac myocytes: Methods for cellular genetic physiology, American Journal of Physiology. Heart and Circulatory Physiology, 279, H429, 10.1152/ajpheart.2000.279.1.H429