Literature DB >> 11948681

Cortisol regulates the expression of Notch in osteoblasts.

Rosa M R Pereira1, Anne M Delany, Deena Durant, Ernesto Canalis.   

Abstract

Glucocorticoids have important effects on osteoblastic replication, differentiation, and function, and the Notch family of receptors is considered to play a role in osteoblastic cell differentiation. We postulated that cortisol could regulate Notch and Notch ligand expression in osteoblastic cells, providing an additional mechanism by which glucocorticoids could regulate osteoblastic differentiation. We examined the expression and regulation of Notch1, 2, 3, and 4 and their ligands Jagged 1 and 2 and Delta 1 and 3 by cortisol in cultures of osteoblastic MC3T3-E1 cells. Cortisol caused a time-dependent increase in Notch1 and 2 mRNA levels in MC3T3 cells. Notch3 and 4 were not detected in the presence or absence of cortisol. MC3T3 cells expressed Delta 1 and Jagged 1 but not Jagged 2 or Delta 3 mRNAs, and cortisol did not have a substantial effect on the expression of any of these ligands. Cortisol increased the rate of Notch1 and 2 transcription and, in transcriptionally arrested cells, did not modify the decay of the transcripts, indicating a transcriptional level of control. In conclusion, cortisol stimulates Notch1 and 2 transcription in osteoblasts. Since Notch signaling appears to play a negative role in osteoblastic differentiation, its increased expression could be relevant to the actions of cortisol in bone. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 11948681     DOI: 10.1002/jcb.10125

Source DB:  PubMed          Journal:  J Cell Biochem        ISSN: 0730-2312            Impact factor:   4.429


  31 in total

1.  Notch signaling in osteocytes differentially regulates cancellous and cortical bone remodeling.

Authors:  Ernesto Canalis; Douglas J Adams; Adele Boskey; Kristen Parker; Lauren Kranz; Stefano Zanotti
Journal:  J Biol Chem       Date:  2013-07-24       Impact factor: 5.157

Review 2.  Glucocorticoid-Induced Osteoporosis.

Authors:  Baruch Frenkel; Wendy White; Jan Tuckermann
Journal:  Adv Exp Med Biol       Date:  2015       Impact factor: 2.622

Review 3.  Mechanisms of glucocorticoid action in bone.

Authors:  Ernesto Canalis
Journal:  Curr Osteoporos Rep       Date:  2005-09       Impact factor: 5.096

4.  Glucocorticoid and growth factor synergism requirement for Notch4 chromatin domain activation.

Authors:  Jing Wu; Emery H Bresnick
Journal:  Mol Cell Biol       Date:  2007-01-12       Impact factor: 4.272

Review 5.  Communications between bone cells and hematopoietic stem cells.

Authors:  R L Porter; L M Calvi
Journal:  Arch Biochem Biophys       Date:  2008-04-07       Impact factor: 4.013

Review 6.  Bone involvement in exogenous hypercortisolism.

Authors:  L Sinigaglia; D Mazzocchi; M Varenna
Journal:  J Endocrinol Invest       Date:  2008-04       Impact factor: 4.256

Review 7.  The niche as a target for hematopoietic manipulation and regeneration.

Authors:  Rialnat A Lawal; Laura M Calvi
Journal:  Tissue Eng Part B Rev       Date:  2011-09-27       Impact factor: 6.389

Review 8.  Hajdu-Cheney Syndrome, a Disease Associated with NOTCH2 Mutations.

Authors:  Ernesto Canalis; Stefano Zanotti
Journal:  Curr Osteoporos Rep       Date:  2016-08       Impact factor: 5.096

9.  Notch1 and Notch2 expression in osteoblast precursors regulates femoral microarchitecture.

Authors:  Stefano Zanotti; Ernesto Canalis
Journal:  Bone       Date:  2014-02-04       Impact factor: 4.398

Review 10.  Pathogenesis of glucocorticoid-induced osteoporosis and options for treatment.

Authors:  Pojchong Chotiyarnwong; Eugene V McCloskey
Journal:  Nat Rev Endocrinol       Date:  2020-04-14       Impact factor: 43.330

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