Increased collagen within the transverse tubules in human heart failure

Cardiovascular Research - Tập 113 Số 8 - Trang 879-891 - 2017
David J. Crossman1, Xin Shen1, Mia Jüllig2, Michelle L. Munro1, Yufeng Hou1, Martin Middleditch2, Darshan Shrestha1, Amy Li3, Sean Lal3, Cristobal G. dos Remedios3, David Baddeley4, Peter Ruygrok5, Christian Soeller1,6
1Department of Physiology, Faculty of Medical and Health Sciences, University of Auckland, 85 Park Road, Grafton, Auckland, 1023, New Zealand
2School of Biological Sciences, University of Auckland, 3A Symonds Street, Auckland 1010, New Zealand
3Bosch Institute, University of Sydney, Fisher Road Sydney, NSW 2006, Australia;
4Department of Cell Biology, Yale University, West Campus, 300 Heffernan Drive, Haven, CT 06515, USA;
5Department of Cardiology, Auckland City Hospital, Auckland 1042, New Zealand;
6Living Systems Institute and Biomedical Physics, University of Exeter, Stocker Road, Exeter EX4QL, UK

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Orchard, 2008, t-tubules and sarcoplasmic reticulum function in cardiac ventricular myocytes, Cardiovasc Res, 77, 237, 10.1093/cvr/cvm002

Bers, 2002, Cardiac excitation–contraction coupling, Nature, 415, 198, 10.1038/415198a

Guo, 2013, Emerging mechanisms of T-tubule remodelling in heart failure, Cardiovasc Res, 98, 204, 10.1093/cvr/cvt020

Franzini-Armstrong, 1999, Shape, size, and distribution of Ca(2+) release units and couplons in skeletal and cardiac muscles, Biophys J, 77, 1528, 10.1016/S0006-3495(99)77000-1

Song, 2006, Orphaned ryanodine receptors in the failing heart, Proc Natl Acad Sci U S A, 103, 4305, 10.1073/pnas.0509324103

Louch, 2006, T-tubule disorganization and reduced synchrony of Ca2+ release in murine cardiomyocytes following myocardial infarction, J Physiol, 574, 519, 10.1113/jphysiol.2006.107227

Heinzel, 2008, Remodeling of T-tubules and reduced synchrony of Ca2+ release in myocytes from chronically ischemic myocardium, Circ Res, 102, 338, 10.1161/CIRCRESAHA.107.160085

Wei, 2010, T-tubule remodeling during transition from hypertrophy to heart failure, Circ Res, 107, 520, 10.1161/CIRCRESAHA.109.212324

Sacconi, 2012, Action potential propagation in transverse-axial tubular system is impaired in heart failure, Proc Natl Acad Sci U S A, 109, 5815, 10.1073/pnas.1120188109

Crocini, 2014, Defects in T-tubular electrical activity underlie local alterations of calcium release in heart failure, Proc Natl Acad Sci U S A, 111, 15196, 10.1073/pnas.1411557111

Ibrahim, 2013, Reversibility of T-tubule remodelling in heart failure: mechanical load as a dynamic regulator of the T-tubules, Cardiovasc Res, 98, 225, 10.1093/cvr/cvt016

Kostin, 1998, The internal and external protein scaffold of the T-tubular system in cardiomyocytes, Cell Tissue Res, 294, 449, 10.1007/s004410051196

Heling, 2000, Extracellular Proteins in Failing Human Myocardium, Circ Res, 846, 10.1161/01.RES.86.8.846

Louch, 2004, Reduced synchrony of Ca2+ release with loss of T-tubules—a comparison to Ca2+ release in human failing cardiomyocytes, Cardiovasc Res, 62, 63, 10.1016/j.cardiores.2003.12.031

Cannell, 2006, Effect of changes in action potential spike configuration, junctional sarcoplasmic reticulum micro-architecture and altered t-tubule structure in human heart failure, J Muscle Res Cell Motil, 27, 297, 10.1007/s10974-006-9089-y

Lyon, 2009, Loss of T-tubules and other changes to surface topography in ventricular myocytes from failing human and rat heart, Proc Natl Acad Sci U S A, 106, 6854, 10.1073/pnas.0809777106

Crossman, 2011, Changes in the organization of excitation-contraction coupling structures in failing human heart, PLoS One, 6, e17901, 10.1371/journal.pone.0017901

Crossman, 2015, t-tubule disease: relationship between t-tubule organization and regional contractile performance in human dilated cardiomyopathy, J Mol Cell Cardiol Elsevier B.V, 84, 170, 10.1016/j.yjmcc.2015.04.022

Hohendanner, 2013, Intracellular dyssynchrony of diastolic cytosolic [Ca2+] decay in ventricular cardiomyocytes in cardiac remodeling and human heart failure, Circ Res, 113, 527, 10.1161/CIRCRESAHA.113.300895

Zhang, 2014, Microtubule-mediated defects in junctophilin-2 trafficking contribute to myocyte T-tubule remodeling and Ca2+ handling dysfunction in heart failure, Circulation, 129, 1742, 10.1161/CIRCULATIONAHA.113.008452

Wu, 2014, Calpain-dependent cleavage of junctophilin-2 and T-tubule remodeling in a mouse model of reversible heart failure, J Am Heart Assoc, 3, e000527, 10.1161/JAHA.113.000527

Guo, 2014, Overexpression of junctophilin-2 does not enhance baseline function but attenuates heart failure development after cardiac stress, Proc Natl Acad Sci U S A, 111, 12240, 10.1073/pnas.1412729111

Oort, 2011, Disrupted junctional membrane complexes and hyperactive ryanodine receptors after acute junctophilin knockdown in mice, Circulation, 123, 979, 10.1161/CIRCULATIONAHA.110.006437

Caldwell, 2014, Dependence of cardiac transverse tubules on the BAR domain protein amphiphysin II (BIN-1), Circ Res, 115, 986, 10.1161/CIRCRESAHA.116.303448

Hong, 2014, Cardiac BIN1 folds T-tubule membrane, controlling ion flux and limiting arrhythmia, Nat Med, 20, 624, 10.1038/nm.3543

Ibrahim, 2013, A critical role for Telethonin in regulating t-tubule structure and function in the mammalian heart, Hum Mol Genet, 22, 372, 10.1093/hmg/dds434

Campbell, 1989, Association of dystrophin and an integral membrane glycoprotein, Nature, 338, 259, 10.1038/338259a0

Verhaert, 2011, Cardiac involvement in patients with muscular dystrophies magnetic resonance imaging phenotype and genotypic considerations, Circ Cardiovasc Imaging, 4, 67, 10.1161/CIRCIMAGING.110.960740

Lapidos, 2004, The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma, Circ Res, 94, 1023, 10.1161/01.RES.0000126574.61061.25

Vatta, 2002, Molecular remodelling of dystrophin in patients with end-stage cardiomyopathies and reversal in patients on assistance-device therapy, Lancet, 359, 936, 10.1016/S0140-6736(02)08026-1

Kaprielian, 2000, Distinct patterns of dystrophin organization in myocyte sarcolemma and transverse tubules of normal and diseased human myocardium, Circulation, 101, 2586, 10.1161/01.CIR.101.22.2586

Allamand, 2011, ColVI myopathies: where do we stand, where do we go?, Skelet Muscle BioMed Central Ltd, 1, 30, 10.1186/2044-5040-1-30

Soeller, 1999, Cardiac rat myocytes by 2-photon microscopy and digital image–processing techniques, Circ Res, 84, 266, 10.1161/01.RES.84.3.266

Camelliti, 2005, Structural and functional characterisation of cardiac fibroblasts, Cardiovasc Res, 65, 40, 10.1016/j.cardiores.2004.08.020

Crossman, 2005, Combining confocal and single molecule localisation microscopy: a correlative approach to multi-scale tissue imaging, Methods, 88, 45

Baddeley, 2011, 4D super-resolution microscopy with conventional fluorophores and single wavelength excitation in optically thick cells and tissues, PLoS One, 6, e20645, 10.1371/journal.pone.0020645

Tokunaga, 2008, Highly inclined thin illumination enables clear single-molecule imaging in cells, Nat Methods, 5, 159, 10.1038/nmeth1171

Baddeley, 2010, Visualization of localization microscopy data, Microsc Microanal, 16, 64, 10.1017/S143192760999122X

Sipilä, 2007, Secretion and assembly of type IV and VI collagens depend on glycosylation of hydroxylysines, J Biol Chem, 282, 33381, 10.1074/jbc.M704198200

Aper, 2014, Colorful protein-based fluorescent probes for collagen imaging, PLoS One, 9, 1, 10.1371/journal.pone.0114983

Hamdani, 2010, More severe cellular phenotype in human idiopathic dilated cardiomyopathy compared to ischemic heart disease, J Muscle Res Cell Motil, 31, 289, 10.1007/s10974-010-9231-8

Abdullah, 2014, Characterization of diffuse fibrosis in the failing human heart via diffusion tensor imaging and quantitative histological validation, NMR Biomed, 27, 1378, 10.1002/nbm.3200

Gunja-Smith, 1996, Remodeling of human myocardial collagen in idiopathic dilated cardiomyopathy. Role of metalloproteinases and pyridinoline cross-links, Am J Pathol, 148, 1639

Segura, 2014, Fibrosis and heart failure, Heart Fail Rev, 19, 173, 10.1007/s10741-012-9365-4

Zou, 2008, Muscle interstitial fibroblasts are the main source of collagen VI synthesis in skeletal muscle: implications for congenital muscular dystrophy types Ullrich and Bethlem, J Neuropathol Exp Neurol, 67, 144, 10.1097/nen.0b013e3181634ef7

Zhang, 2013, Ultrastructural uncoupling between T-tubules and sarcoplasmic reticulum in human heart failure, Cardiovasc Res, 98, 269, 10.1093/cvr/cvt030

Engvall, 1986, Molecular assembly, secretion, and matrix deposition of type VI collagen, J Cell Biol, 102, 703, 10.1083/jcb.102.3.703

Fitzgerald, 2008, Three novel collagen VI chains, α4(VI), α5(VI), and α6(VI), J Biol Chem, 283, 20170, 10.1074/jbc.M710139200

Gara, 2008, Three novel collagen VI chains with high homology to the α3 chain, J Biol Chem, 283, 10658, 10.1074/jbc.M709540200

Holden, 2014, Characterization of the alpha 6 chain of collagen VI collagen : implications for macromolecular assembly and function ORS, Trans Annu Meeting Orthopaed Res Soc, 59, 1237

Holden, 2013, Unique distribution of the α6 chain of collagen VI in skeletal muscle, Trans Annu Meeting Orthopaed Res Soc, 58, 1408

Uhlen, 2015, Tissue-based map of the human proteome, Science, 347, 1260419, 10.1126/science.1260419

Wiberg, 2002, Biglycan organizes collagen VI into hexagonal-like networks resembling tissue structures, J Biol Chem, 277, 49120, 10.1074/jbc.M206891200

Rafii, 2006, Biglycan binds to α- and γ-sarcoglycan and regulates their expression during development, J Cell Physiol, 209, 439, 10.1002/jcp.20740

Wiberg, 2001, Biglycan and decorin bind close to the N-terminal region of the collagen VI triple helix, J Biol Chem, 276, 18947, 10.1074/jbc.M100625200

Renley, 1998, Dystrophin binding to nonmuscle actin, Cell Motil Cytoskeleton, 41, 264, 10.1002/(SICI)1097-0169(1998)41:3<264::AID-CM7>3.0.CO;2-Z

Prins, 2009, Dystrophin is a microtubule-associated protein, J Cell Biol, 186, 363, 10.1083/jcb.200905048

Viola, 2014, Impaired functional communication between the L-type calcium channel and mitochondria contributes to metabolic inhibition in the mdx heart, Proc Natl Acad Sci U S A, 111, E2905, 10.1073/pnas.1402544111

Cheng, 2012, Focal but reversible diastolic sheet dysfunction reflects regional calcium mishandling in dystrophic mdx mouse hearts, AJP Hear Circ Physiol, 303, H559, 10.1152/ajpheart.00321.2012

Fitzgerald, 2014, A mutation in the alpha 6 chain of type VI collagen disrupts E-C coupling and leads to a lethal muscular dystrophy, Trans Annu Meeting Orthopaed Res Soc, 58, 527

McNary, 2011, Strain transfer in ventricular cardiomyocytes to their transverse tubular system revealed by scanning confocal microscopy, Biophys J Biophysical Soc, 100, L53

Mollnau, 1995, Collagen VI in the extracellular matrix of normal and failing human myocardium, Herz, 20, 89

Luther, 2012, Absence of type VI collagen paradoxically improves cardiac function, structure, and remodeling after myocardial infarction, Circ Res, 110, 851, 10.1161/CIRCRESAHA.111.252734

Wei, 2000, Effect of carvedilol in comparison with metoprolol on myocardial collagen postinfarction, J Am Coll Cardiol, 36, 276, 10.1016/S0735-1097(00)00671-9

Chen, 2012, β-Adrenergic receptor antagonists ameliorate myocyte T-tubule remodeling following myocardial infarction, FASEB J, 26, 2531, 10.1096/fj.11-199505