Alpha 1-adrenergic stimulation of cardiac gene transcription in neonatal rat myocardial cells. Effects on myosin light chain-2 gene expression
- PMID: 2835372
Alpha 1-adrenergic stimulation of cardiac gene transcription in neonatal rat myocardial cells. Effects on myosin light chain-2 gene expression
Abstract
Previous studies have demonstrated that alpha-adrenergic stimulation of cultured, neonatal rat myocardial cells results in an increase in intracellular volume and protein content of cultured neonatal rat myocardial cells. Utilizing this model of cardiac hypertrophy, we have examined the effects of alpha-adrenergic stimulation on the accumulation of sarcomeres and the expression of a rat cardiac myofibrillar gene, myosin light chain-2 (MLC-2). Following alpha-adrenergic stimulation, cultured myocardial cells displayed a severalfold increase in the number of sarcomeric units, as assessed by electron microscopy, an increase in cellular MLC-2 content, and a 2-3 fold increase in the steady state levels of MLC-2 mRNA. This effect of alpha-adrenergic stimulation was accompanied by a 2-3-fold increase in total transcriptional activity, which was dependent on the concentration and duration of exposure to the agonist, and displayed alpha 1-adrenergic receptor specificity. The transcriptional response was not immediate, with a lag period of at least 1 h, and a maximal effect required continuous occupancy of the receptor. The increase in steady state levels of MLC-2 mRNA is regulated, in part, at the level of transcription of the cardiac MLC-2 gene. These results suggest that alpha 1-adrenergic stimulation may be important in the growth of the neonatal heart through the activation of total transcriptional activity. In addition, increases in the levels of myofibrillar proteins during myocardial cell growth and hypertrophy, may be mediated in part by the stimulation of transcription of myofibrillar genes.
Similar articles
-
Alpha- and beta-adrenergic stimulation induces distinct patterns of immediate early gene expression in neonatal rat myocardial cells. fos/jun expression is associated with sarcomere assembly; Egr-1 induction is primarily an alpha 1-mediated response.J Biol Chem. 1990 Aug 15;265(23):13809-17. J Biol Chem. 1990. PMID: 1696258
-
Alpha 1-adrenergic receptor stimulation of sarcomeric actin isogene transcription in hypertrophy of cultured rat heart muscle cells.J Clin Invest. 1989 Mar;83(3):1078-82. doi: 10.1172/JCI113951. J Clin Invest. 1989. PMID: 2537847 Free PMC article.
-
Alpha1-adrenergic regulation of peptidylglycine alpha-amidating monooxygenase gene expression in cultured rat cardiac myocytes: transcriptional studies and messenger ribonucleic acid stability.Mol Cell Endocrinol. 1999 Aug 20;154(1-2):89-100. doi: 10.1016/s0303-7207(99)00084-2. Mol Cell Endocrinol. 1999. PMID: 10509804
-
Phorbol esters induce immediate-early genes and activate cardiac gene transcription in neonatal rat myocardial cells.J Mol Cell Cardiol. 1990 Aug;22(8):901-10. doi: 10.1016/0022-2828(90)90121-h. J Mol Cell Cardiol. 1990. PMID: 2122001
-
Transcription of early developmental isogenes in cardiac myocyte hypertrophy.J Mol Cell Cardiol. 1989 Dec;21 Suppl 5:79-89. doi: 10.1016/0022-2828(89)90774-8. J Mol Cell Cardiol. 1989. PMID: 2560798 Review.
Cited by
-
Adrenergic agents, but not triiodo-L-thyronine induce c-fos and c-myc expression in the rat heart.Basic Res Cardiol. 1991 Mar-Apr;86(2):154-64. doi: 10.1007/BF02190548. Basic Res Cardiol. 1991. PMID: 1908674
-
Mitogen-activated protein kinase phosphatase 1 inhibits the stimulation of gene expression by hypertrophic agonists in cardiac myocytes.Biochem J. 1997 Apr 15;323 ( Pt 2)(Pt 2):313-9. doi: 10.1042/bj3230313. Biochem J. 1997. PMID: 9163318 Free PMC article.
-
Myocardial expression of a constitutively active alpha 1B-adrenergic receptor in transgenic mice induces cardiac hypertrophy.Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):10109-13. doi: 10.1073/pnas.91.21.10109. Proc Natl Acad Sci U S A. 1994. PMID: 7937846 Free PMC article.
-
Mitogen-activated protein kinases mediate changes in gene expression, but not cytoskeletal organization associated with cardiac muscle cell hypertrophy.J Cell Biol. 1994 Sep;126(6):1565-72. doi: 10.1083/jcb.126.6.1565. J Cell Biol. 1994. PMID: 8089186 Free PMC article.
-
RGS4 causes increased mortality and reduced cardiac hypertrophy in response to pressure overload.J Clin Invest. 1999 Sep;104(5):567-76. doi: 10.1172/JCI6713. J Clin Invest. 1999. PMID: 10487771 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical