Survey of studies examining mammalian cardiomyocyte DNA synthesis

Circulation Research

Volumn 83, Issue 1, 1998, Pages 15-26

  Soonpaa, Mark H ^a   Field, Loren J ^a  

^a INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Cardiomyocyte; Development; DNA synthesis

Indexed keywords

CELL CYCLE; CELL PROLIFERATION; CELL ULTRASTRUCTURE; DNA SYNTHESIS; GENE EXPRESSION; GENE REPLICATION; HEART MUSCLE CELL; HISTOLOGY; HUMAN; PRIORITY JOURNAL; REVIEW;

EID: 0032514229     PISSN: 00097330     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.RES.83.1.15     Document Type: Review

References (47)

1. Eldridge SR, Goldsworthy SM. Cell proliferation rates in common cancer target tissues of B6C3F1 mice and F344 rats: effects of age, gender, and choice of marker. Fundam Appl Toxicol. 1996;32:159-167.
2. Maiolino P, Restucci B, De Vico G. Expression of proliferating cell nuclear antigen in basal cell carcinomas and in squamous cell carcinomas of canine skin: correlation with mitotic index and histological features. Zentralbl Veterinarmed A. 1995;42:339-343.
3. Connolly KM, Bogdanffy MS. Evaluation of proliferating cell nuclear antigen (PCNA) as an endogenous marker of cell proliferation in rat liver: a dual-stain comparison with 5-bromo-2′-deoxyuridine. J Histochem Cytochem. 1993;41:1-6.
4. Chapman DL, Wolgemuth DJ. Expression of proliferating cell nuclear antigen in the mouse germ line and surrounding somatic cells suggests both proliferation-dependent and -independent modes of function. Int J Dev Biol. 1994;38:491-497.
5. Pandey S, Wang E. Cells en route to apoptosis are characterized by the upregulation of c-fos, c-myc, c-jun, cdc2, and RB phosphorylation, resembling events of early cell-cycle traverse. J Cell Biochem. 1995;58:135-150.
6. Hall PA, Coates PJ, Goodlad RA, Hart IR, Lane DP. Proliferating cell nuclear antigen expression in non-cycling cells may be induced by growth factors in vivo. Br J Cancer. 1994;70:244-247.
7. Soonpaa MH, Koh GY, Klug MG, Field LJ. Formation of nascent intercalated disks between grafted fetal cardiomyocytes and host myocardium. Science. 1994;264:98-101.
8. Soonpaa MH, Field LJ: Assessment of cardiomyocyte DNA synthesis in normal and injured adult mouse hearts. Am J Physiol. 1997;272:H220-H226.
9. Cheng W, Reiss K, Kajstura J, Kowal K, Quaini F, Anversa P. Down-regulation of the IGF-1 system parallels the attenuation in the proliferative capacity of rat ventricular myocytes during postnatal development. Lab Invest. 1995;72:646-655.
10. Marino TA, Haldar S, Williamson EC, Beaverson K, Walter RA, Marino DR, Beatty C, Lipson KE. Proliferating cell nuclear antigen in developing and adult rat cardiac muscle cells. Circ Res. 1991;69:1353-1360.
11. Clubb FJ Jr, Bishop SP. Formation of binucleated myocardial cells in the neonatal rat: an index for growth hypertrophy. Lab Invest. 1984;50:571-577.
12. Sasaki R, Morishita T, Yamagata S. Mitosis of heart muscle cells in normal rats. Tohoku J Exp Med. 1968;96:405-411.
13. Sasaki R, Morishita T, Yamagata S. Autoradiographic studies on heart muscle cells in normal rats. Tohoku J Exp Med. 1970;100:1-13.
14. Li F, Wang X, Capasso JM, Gerdes AM. Rapid transition of cardiac myocytes from hyperplasia to hypertrophy during postnatal development. J Mol Cell Cardiol. 1996;28:1737-1746.
15. Marino TA, Cao W, Lee J, Courtney R. Localization of proliferating cell nuclear antigen in the developing and mature rat heart cell. Anat Rec. 1996;245:677-684.
16. Nag AC, Carey TR, Cheng M. DNA synthesis in rat heart cells after injury and the regeneration of myocardia. Tissue Cell. 1983;15:597-613.
17. Wachtlova M, Mares V, Ostadal B. DNA synthesis in the ventricular myocardium of young rats exposed to intermittent high altitude (IHA) hypoxia: an autoradiographic study. Virchows Arch B Cell Pathol. 1977;24:335-342.
18. Rumyantsev PP, Borisov A. DNA synthesis in myocytes from different myocardial compartments of young rats in norm, after experimental infarction and in vitro. Biomed Biochim Acta. 1987;46:S610-S615.
19. Baba HA, Takeda A, Schmid C, Nagano M. Early proliferative changes in hearts of hypertensive Goldblatt rats: an immunohistochemical and flow-cytometrical study. Basic Res Cardiol. 1996;91:275-282.
20. Kajstura J, Zhang X, Reiss K, Szoke E, Li P, Lagrasta C, Cheng W, Darzynkiewicz Z, Olivetti G, Anversa P. Myocyte cellular hyperplasia and myocyte cellular hypertrophy contribute to chronic ventricular remodeling in coronary artery narrowing-induced cardiomyopathy in rats. Circ Res. 1994;74:383-400.
21. Reiss K, Kajstura J, Capasso JM, Marino TA, Anversa P. Impairment of myocyte contractility following coronary artery narrowing is associated with activation of the myocyte IGF1 autocrine system, enhanced expression of late growth related genes, DNA synthesis, and myocyte nuclear mitotic division in rats. Exp Cell Res. 1993;207:348-360.
22. Kuhn H, Pfitzer P, Stoepel K. DNA content and DNA synthesis in the myocardium of rats after induced renal hypertension. Cardiovasc Res. 1974;8:86-91.
23. Rumyantsev PP, Marakjan VO. Reactive synthesis of DNA and mitotic division in atrial heart muscle cells following ventricle infarction. Experientia. 1968;24:1234-1235.
24. Oberpriller JO, Ferrans VJ, Carroll RJ. DNA synthesis in rat atrial myocytes as a response to left ventricular infarction: an autoradiographic study of enzymatically dissociated myocytes. J Mol Cell Cardiol. 1984;16:1119-1126.
25. Rumjantsev PP. DNA synthesis and mitoses in atrial myocytes of rats with aortal stenosis. Experientia. 1970;26:773-774.
26. Morkin E, Ashford TP. Myocardial DNA synthesis in experimental cardiac hypertrophy. Am J Physiol. 1968;215:1409-1413.
27. Reiss K, Meggs LG, Li P, Olivetti G, Capasso JM, Anversa P. Upregulation of IGF1, IGF1-receptor, and late growth related genes in ventricular myocytes acutely after infarction in rats. J Cell Physiol. 1994;158:160-168.
28. Heron MI, Rakusan K. Proliferating cell nuclear antigen (PCNA) detection of cellular proliferation in hypothyroid and hyperthyroid rat hearts. J Mol Cell Cardiol. 1995;27:1393-1403.
29. Anversa P, Fitzpatrick D, Argani S, Capasso JM. Myocyte mitotic division in the aging mammalian rat heart. Circ Res. 1991;69:1159-1164.
30. Erokhina IL, Rumyantsev PP. Ultrastructure of DNA-synthesizing and mitotically dividing myocytes in sinoatrial node of mouse embryonal heart. J Mol Cell Cardiol. 1986;18:1219-1231.
31. Soonpaa MH, Kim KK, Pajak L, Franklin M, Field LJ. Cardiomyocyte DNA synthesis and binucleation during murine development. Am J Physiol. 1996;271:H2183-H2189.
32. Machida N, Brisse N, Sreenan C, Bishop SP. Inhibition of cardiac myocyte division in c-myc transgenic mice. J Mol Cell Cardiol. 1997;29:1895-1902.
33. Brodsky WY, Arefyeva AM, Uryvaeva IV. Mitotic polyploidization of mouse heart myocytes during the first postnatal week. Cell Tissue Res. 1980;210:133-144.
34. Petersen RO, Baserga R. Nucleic acid and protein synthesis in cardiac muscle of growing and adult mice. Exp Cell Res. 1965;40:340-352.
35. Nakagawa M, Hamaoka K, Hattori T, Sawada T. Postnatal DNA synthesis in hearts of mice: autoradiographic and cytofluorometric investigations. Cardiovasc Res. 1988;22:575-583.
36. Soonpaa MH, Field LJ. Assessment of cardiomyocyte DNA synthesis during hypertrophy in adult mice. Am J Physiol. 1994;266:H1439-H1445.
37. Soonpaa MH, Koh GY, Pajak L, Jing S, Wang H, Franklin MT, Kim KK, Field LJ. Cyclin D1 overexpression promotes cardiomyocyte DNA synthesis and multinucleation in transgenic mice. J Clin Invest. 1997;99: 2644-2654.
38. Rumyantsev PP. Autoradiographic study on the synthesis of DNA, RNA, and proteins in normal cardiac muscle cells and those changed by experimental injury. Folia Histochem Cytochem. 1966;4:397-424.
39. Rumyantsev PP. Ultrastructural reorganization, DNA synthesis and mitotic division of myocytes in atria of rats with left ventricle infarction: an electron microscopic and autoradiographic study. Virchows Arch B Cell Pathol. 1974;15:357-378.
40. Rumyantsev PP. DNA synthesis in atrial myocytes of rats with aortic stenosis. Adv Myocardiol. 1983;4:147-162.
41. Sasaki R, Morishita T, Ichikawa S, Yamagata S. Autoradiographic studies and mitosis of heart muscle cells in experimental cardiac hypertrophy. Tohoku J Exp Med. 1970;102:159-167.
42. Meerson FZ, Alekhina GM, Aleksandrov PN, Bazardjan AG. Dynamics of nucleic acid and protein synthesis of the myocardium in compensatory hyperfunction and hypertrophy of the heart. Am J Cardiol. 1968;22:337-348.
43. Erokhina IL, Rumyantsev PP. Proliferation and biosynthetic activities of myocytes from the conductive system and working myocardium of the developing mouse heart: light microscopic autoradiographic study. Acta Histochem. 1988;84:51-56.
44. Kirshenbaum LA, Abdellatif M, Chakraborty S, Schneider MD. Human E2F-1 reactivates cell cycle progression in ventricular myocytes and represses cardiac gene transcription. Dev Biol. 1996;179:402-411.
45. Kirshenbaum LA, Schneider MD. Adenovirus E1A represses cardiac gene transcription and reactivates DNA synthesis in ventricular myocytes, via alternative pocket protein- and p300-binding domains. J Biol Chem. 1995;270:7791-7794.
46. Liu Y, Kitsis RN. Induction of DNA synthesis and apoptosis in cardiac myocytes by E1A oncoprotein. J Cell Biol. 1996;133:325-334.
47. Claycomb WC, Bradshaw HD Jr. Acquisition of multiple nuclei and the activity of DNA polymerase alpha and reinitiation of DNA replication in terminally differentiated adult cardiac muscle cells in culture. Dev Biol. 1983;99:331-337.