Induction of the vitamin D 24-hydroxylase (CYP24) by 1,25- dihydroxyvitamin D3 is regulated by parathyroid hormone in UMR106 osteoblastic cells

H. J. Armbrecht, T. L. Hodam, M. A. Boltz, Nicola Partridge, A. J. Brown, V. B. Kumar

Research output: Contribution to journalArticle

Abstract

The expression of the vitamin D 24-hydroxylase is highly regulated in target tissues for 1,25-dihydroxyvitamin D3 (1, 25(OH)2D), where it may modulate the action of 1,25(OH)2D. In UMR106 osteoblastic cells, 1,25(OH)2D and PTH synergistically induce 24-hydroxylase expression. The purpose of these studies was to characterize the interaction between 1,25(OH)2D and PTH with regard to the messenger RNA (mRNA) levels of the cytochrome P450 component of the 24-hydroxylase (CYP24). PTH alone had no effect on CYP24 mRNA levels, and 1,25(OH)2D alone produced only a modest increase. However, 1,25(OH)2D and PTH together synergistically increased CYP24 mRNA levels 3- fold compared with 1,25(OH)2D alone. PTH also in- creased the sensitivity of UMR cells to 1,25(OH)2D from 10-8 to 10-10 M. PTH worked through the cAMP signaling pathway as evidenced by the lack of effect of PTH (3-34) and by the full activity of 8-bromo-cAMP. PTH in the presence of 1,25(OH)2D increased CYP24 gene transcription as shown by nuclear run-on studies and by activation of a CYP24 promoter-reporter construct after transfection. PTH also increased vitamin D receptor number in UMR cells, but this occurred at times later than the increase in transcription. These studies demonstrate that PTH in the presence of 1,25(OH)2D works through the cAMP-dependent signaling pathway to increase transcription of the CYP24 gene, to increase CYP24 protein levels, and to increase 24-hydroxylase activity.

Original languageEnglish (US)
Pages (from-to)3375-3381
Number of pages7
JournalEndocrinology
Volume139
Issue number8
DOIs
StatePublished - 1998

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Mixed Function Oxygenases
Parathyroid Hormone
Cytochrome P-450 Enzyme System
Messenger RNA
8-Bromo Cyclic Adenosine Monophosphate
Vitamin D3 24-Hydroxylase
Calcitriol Receptors
Calcitriol
Genes
Transfection

ASJC Scopus subject areas

  • Endocrinology
  • Endocrinology, Diabetes and Metabolism

Cite this

Induction of the vitamin D 24-hydroxylase (CYP24) by 1,25- dihydroxyvitamin D3 is regulated by parathyroid hormone in UMR106 osteoblastic cells. / Armbrecht, H. J.; Hodam, T. L.; Boltz, M. A.; Partridge, Nicola; Brown, A. J.; Kumar, V. B.

In: Endocrinology, Vol. 139, No. 8, 1998, p. 3375-3381.

Research output: Contribution to journalArticle

Armbrecht, H. J. ; Hodam, T. L. ; Boltz, M. A. ; Partridge, Nicola ; Brown, A. J. ; Kumar, V. B. / Induction of the vitamin D 24-hydroxylase (CYP24) by 1,25- dihydroxyvitamin D3 is regulated by parathyroid hormone in UMR106 osteoblastic cells. In: Endocrinology. 1998 ; Vol. 139, No. 8. pp. 3375-3381.
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abstract = "The expression of the vitamin D 24-hydroxylase is highly regulated in target tissues for 1,25-dihydroxyvitamin D3 (1, 25(OH)2D), where it may modulate the action of 1,25(OH)2D. In UMR106 osteoblastic cells, 1,25(OH)2D and PTH synergistically induce 24-hydroxylase expression. The purpose of these studies was to characterize the interaction between 1,25(OH)2D and PTH with regard to the messenger RNA (mRNA) levels of the cytochrome P450 component of the 24-hydroxylase (CYP24). PTH alone had no effect on CYP24 mRNA levels, and 1,25(OH)2D alone produced only a modest increase. However, 1,25(OH)2D and PTH together synergistically increased CYP24 mRNA levels 3- fold compared with 1,25(OH)2D alone. PTH also in- creased the sensitivity of UMR cells to 1,25(OH)2D from 10-8 to 10-10 M. PTH worked through the cAMP signaling pathway as evidenced by the lack of effect of PTH (3-34) and by the full activity of 8-bromo-cAMP. PTH in the presence of 1,25(OH)2D increased CYP24 gene transcription as shown by nuclear run-on studies and by activation of a CYP24 promoter-reporter construct after transfection. PTH also increased vitamin D receptor number in UMR cells, but this occurred at times later than the increase in transcription. These studies demonstrate that PTH in the presence of 1,25(OH)2D works through the cAMP-dependent signaling pathway to increase transcription of the CYP24 gene, to increase CYP24 protein levels, and to increase 24-hydroxylase activity.",
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