Nuclear architecture remodelling in cardiomyocytes with

Folia Neuropathologica

Volumn 46, Issue 3, 2008, Pages 196-203

  Fidziańska, Anna ^a   Walczak, Ewa ^b   Glinka, Zofia ^a   Religa, Grzegorz ^c  

^a MOSSAKOWSKI MEDICAL RESEARCH CENTRE   (Poland)

^b INSTITUTE OF RHEUMATOLOGY   (Poland)

^c INSTITUTE OF CARDIOLOGY   (Poland)

Author keywords

Appearance of mitochondria within nuclear interior; Lamin A deficiency; Nuclear remodelling

Indexed keywords

LAMIN A;

ARTICLE; CASE REPORT; CELL NUCLEUS MATRIX; CELL ULTRASTRUCTURE; CELLULAR DISTRIBUTION; CHROMATIN; CLINICAL EXAMINATION; CONGESTIVE CARDIOMYOPATHY; CONTROLLED STUDY; CYTOARCHITECTURE; ELECTROCARDIOGRAPHY; ELECTROPHYSIOLOGY; HEART MUSCLE BIOPSY; HEART MUSCLE CELL; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; LAMIN A DEFICIENCY; MITOCHONDRION; NUCLEAR LAMINA; NUCLEAR SHAPE; PROTEIN DEFICIENCY; STRUCTURE ANALYSIS; THORAX RADIOGRAPHY;

EID: 55349093922     PISSN: 16414640     EISSN: 1509572X     Source Type: Journal    
DOI: None     Document Type: Article

References (29)

1. Arbustini E, Pasotti M, Pilotto A, Repetto A, Grasso M, Diogoli M. Gene symbol: CMDA1A disease: Dilated cardiomyopathy associated with conduction system disease. Hum Genet 2005; 117: 295.
2. Bakeeva LE, Skulachev VP, Sudarikova YV, Tsyplenkova VG. Mitochondria enter the nucleus (one further problem in chronic alcoholism). Biochemistry (Mosc) 2001; 66: 1335-1341.
3. Ben Yaou R, Gueneau L, Demay L, Stora S, Chikhaoui K, Richard P, Bonne G. Heart involvement in lamin A/C related diseases. Arch Mal Coevr Vaiss 2006; 99: 848-855.
4. Broers JL, Peeters EA, Kuijpers HJ, Endert J, Bouten CV, Oomens CW, Baaijens FP, Ramaekers FC. Decreased mechanical stiffness in LMNA-/- cells is caused by defective nucleo-cytoskeletal integrity: implications for the development of laminopathies. Hum Mol Genet 2004; 13: 2567-2580.
5. Broers JL, Ramaekers FC, Bonne G, Yaou RB, Hutchinson CJ. Nuclear lamins laminopaties and their role in premature aging. Physiol Rev 2006; 86: 967-1008.
6. Decostre V, Ben Yaou R, Bonne G. Laminopathies affecting skeletal and cardiac muscles: clinical and pathophysiological aspects. Acta Myol 2005; 24: 104-109.
7. Fidziańska A, Bilińska ZT, Tesson F, Wagner T, Walski M, Grzybowski J, Ruzytto W, Hausmanowa-Petrusewicz I. Obliteration of cardiomyocyte nuclei architecture in a patient with LMNA gene mutation. J Neurol Sci 2008; 271: 91-96.
8. Fidziańska A, Glinka Z. Nuclear architecture remodeling in envelopathies. Folia Neuropathol 2007; 45: 47-55.
9. Fidziańska A, Hausmanowa-Petrusewicz I. Architectural abnormalities in muscle nuclei. Ultrastructural di. erences between X-linked and autosomal dominant forma of EDMD. J Neurol Sci 2003; 210: 47-51.
10. Filesi I, Gullotta F, Lattanzi G, D'Apice MR, Capanni C, Nardone AM, Columbaro M, Scarano G, Mattioli E, Sabatelli P, Maraldi NM, Biocca S, Novelli G. Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia a rare form of laminopathy. Physiol Genomics 2005; 23: 150-158.
11. Goldman RD, Shumaker DK, Erdos MR, Eriksson M, Goldman AE, Gordon LB, Gruenbaum Y, Khuon S, Mendez M, Varga R, Collins FS. Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome. Proc Natl Acad Sci USA 2004; 101:8963-8968.
12. Gruenbaum Y, Goldman RD, Meyuhas R, Mills E, Margalit A, Fridkin A, Dayani Y, Prokocimer M, Enosh A. The nuclear lamina and its functions in the nucleus. Int Rev Cytol 2003; 226: 1-62.
13. Holaska JM, Wilson KL, Mansharamani M. The nuclear envelope, lamins and nuclear assembly. Curr Opin Cell Biol 2002; 14: 357-364.
14. Hozak P, Sasseville AM, Raymond Y, Cook PR. Lamin proteins from and internal nucleoskeleton as well as peripheral lamina in human cells. J Cell Sci 1995; 108: 635-644.
15. Moir RD, Spann TP, Goldman RD. The dynamic properties and possible functions of nuclear lamins. Int Rev Cytol 1995; 162B: 141-182.
16. Muchir A, van Engelen BG, Lammens M, Mislow JM, McNally E, Schwartz K, Bonne G. Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C gene. Exp Cell Res 2003; 291: 352-362.
17. Nikolova V, Leimena C, McMahon AC, Tan JC, Chandar S, Jogia D, Kesteven SH, Michalicek J, Otway R, Verheyen F, Rainer S, Stewart CL, Martin D, Feneley MP, Fatkin D. Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C deficient mice. J Clin Invest 2004; 113: 567-569.
18. Raharjo WH, Enarson P, Sullivan T, Stewart CL, Burke B. Nuclear envelope defects associated with LMNA mutations cause dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy. J Cell Sci 2001; 114: 4447-4457.
19. Reichart B, Klafke R, Dreger C, Krüger E, Motsch I, Ewald A, Schäfer J, Reichmann H, Müller CR, Dabauvalle MC. Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation. BMC Cell Biol. 2004; 5: 12.
20. Sabatelli P, Lattanzi G, Ognibene A, Columbaro M, Capanni C, Merlini L, Maraldi NM, Squarzoni S. Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy. Muscle Nerve 2001; 24: 826-829.
21. Stuurman N, Heins S, Aebi U. Nuclear lamins: their structure, assembly and interactions. J Struct Biol 1998; 122: 42-66.
22. Sullivan T, Escalante-Alcalde D, Bhatt H, Anver M, Bhat N, Nagashima K, Stewart CL, Burke B. Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy. J Cell Biol 1999; 147: 913-920.
23. Sylvius N, Bilinska ZT, Veinot JP, Fidzianska A, Bolongo PM, Poon S, McKeown P, Davies RA, Chan KL, Tang AS, Dyack S, Grzybowski J, Ruzyllo W, McBride H, Tesson F. In vivo and in vitro examination of functional significances of novel lamin gene mutations in heart failure patients. J Med Genet 2005; 42: 639-647.
24. Wang Y, Herron AJ, Worman HJ. Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy. Hum Mol Genet 2006; 15: 2479-2489.
25. Worman HJ, Bonne G. Laminopathies a wide spectrum of human diseases. Exp Cell Res 2007; 313: 2121-2133.
26. Worman HJ, Courvalin JC. How do mutation in lamins A and C cause disease? J Clin Invest 2004; 113: 349-351.
27. Verga L, Concardi M, Pilotto A, Bellini O, Pasotti M, Repetto A, Tavazzi L, Arbustini E. Loss of lamin A/C expression revealed in immuno-electron microscopy in dilated cardiomyopathy with atrioventricular block caused by LMNA gene defects. Virchows Arch 2003; 443: 664-671.
28. Verstreaten VL, Broers JL, Ramaekers FC, vanSteensel MA. The nuclear envelope a key structure in cellular integrity and gene expression. Curr Med Chem 2007; 14: 1231-1248.
29. Vigouroux C, Auclair M, Dubosclard E, Pouchelet M, Capeau J, Courvalin JC, Buendia B. Nuclear envelope disorganization in fibroblasts from lipodystrophic patients with heterozygous R482Q/W mutations in the lamin A/C gene. J Cell Sci 2001; 114: 4459-4468.