Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2003-5-19
pubmed:abstractText
We previously showed that parathyroid hormone (PTH) induces inducible cAMP early repressor (ICER) in osteoblastic cells and mouse calvariae. PTH signaling in osteoblastic cells is transduced by PTH receptor 1, which is coupled to cAMP-protein kinase A (PKA), protein kinase C (PKC), and calcium signaling pathways. In the present study, we examined the role of these pathways in mediating PTH-induced ICER mRNA and protein expression in osteoblastic MC3T3-E1 cells. Using RT-PCR, we found that PTH(1-34), forskolin (FSK), and 8-bromo-cAMP (8Br-cAMP) induced ICER expression, while phorbol myristate acetate (PMA), ionomycin, and PTH(3-34) did not. Similar results were found for the induction of ICER protein. PKA inhibition by H89 markedly reduced PTH- and FSK-induced ICER expression, while PKC depletion by PMA had little effect. We also tested ICER induction by other osteotropic signaling agonists. Other cAMP-PKA pathway activators, such as PTH-related protein (PTHrP), induced ICER expression, while agents that signal through other pathways did not. PTHrP maximally induced ICER mRNA at 2-4 h, which then returned to baseline by 10 h. Finally, PTH, FSK, and PTHrP induced ICER in cultured mouse calvariae and osteoblastic ROS 17/2.8, UMR-106, and Pyla cells. We conclude that ICER expression in osteoblasts requires activation of the cAMP-PKA signaling pathway.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
8756-3282
pubmed:author
pubmed:issnType
Print
pubmed:volume
32
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
483-90
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:12753864-3T3 Cells, pubmed-meshheading:12753864-Animals, pubmed-meshheading:12753864-Cyclic AMP Response Element Modulator, pubmed-meshheading:12753864-Cyclic AMP-Dependent Protein Kinases, pubmed-meshheading:12753864-DNA-Binding Proteins, pubmed-meshheading:12753864-Enzyme Inhibitors, pubmed-meshheading:12753864-Female, pubmed-meshheading:12753864-Forskolin, pubmed-meshheading:12753864-Gene Expression, pubmed-meshheading:12753864-Mice, pubmed-meshheading:12753864-Mice, Inbred Strains, pubmed-meshheading:12753864-Osteoblasts, pubmed-meshheading:12753864-Parathyroid Hormone, pubmed-meshheading:12753864-Parathyroid Hormone-Related Protein, pubmed-meshheading:12753864-Pregnancy, pubmed-meshheading:12753864-RNA, Messenger, pubmed-meshheading:12753864-Repressor Proteins, pubmed-meshheading:12753864-Signal Transduction, pubmed-meshheading:12753864-Skull
pubmed:year
2003
pubmed:articleTitle
Expression of inducible cAMP early repressor is coupled to the cAMP-protein kinase A signaling pathway in osteoblasts.
pubmed:affiliation
Department of Medicine, University of Connecticut Health Center, Farmington, CT 06030, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't