Differential and dramatic changes of cyclin-dependent kinase activities in cardiomyocytes during the neonatal period

Cited 47 time in webofscience Cited 45 time in scopus
  • Hit : 436
  • Download : 0
The molecular mechanisms that arrest cardiomyocytes in the cell cycle during the postnatal period remain largely unknown. We have examined changes of the expression of cyclins and CDKs, the activity of each CDK in cardiomyocytes during the postnatal period, and have compared those changes with rate of binucleation formation of cardiomyocytes in rats, The mRNA and protein levels of cyclin D1, A and B in cardiomyocytes were high at day 1, then the levels decreased at different rates during the postnatal period. While the protein levels of cyclin A and B rapidly decreased, the protein level of cyclin DI was relatively constant, The protein levels of CDK4, CDK2, and cdc2 in cardiomyocytes were high at day 1, then their levels gradually decreased. However, the activity of CDK4, which is responsible for G1 phase of cell cycle, was detectable only at day 1. The activity of CDK2 activity, which is responsible for the S phase of cell cycle, was relatively high at day I, decreased at day 2, abruptly decreased at day 4, maintained the same low lever until day 10, and barely or not detectable thereafter in cardiomyocytes, The activity of cdc2 was high at day I, increased by 20% at day 2, and then gradually decreased thereafter, although approximately 50% of maximum activity was present at day 6. Most cardiomyocytes were mononucleated during the first 2 days postnatal. The percentage of binucleated cardiomyocytes increased from 2.5% at day 2, 14% at day 4, 50% at day 8, 80% at day 14, and had reached adult levels at day 21 after birth. During active binucleation formation in neonatal (from days 1-14) cardiomyocytes, CDK4 or CDK2 was functionally negligible, while cdc2 was functionally active, These data suggest that there were differential and dramatic decrease of CDK4 and CDK2 activities in cardiomyocytes during neonatal period, and the functionally active cdc2 in neonatal cardiomyocytes may be involved in binucleation formation. (C) 1997 Academic Press Limited.
Publisher
ACADEMIC PRESS LTD ELSEVIER SCIENCE LTD
Issue Date
1997
Language
English
Article Type
Article
Keywords

CELL-CYCLE; G1 PHASE; RAT; MYOCYTES; GROWTH; HEART; HYPERTROPHY; PROLIFERATION; HYPERPLASIA; EXPRESSION

Citation

JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, v.29, pp.1767 - 1777

ISSN
0022-2828
DOI
10.1006/jmcc.1997.0450
URI
http://hdl.handle.net/10203/72635
Appears in Collection
MSE-Journal Papers(저널논문)
Files in This Item
There are no files associated with this item.
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 47 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0