Effect of oncostatin M on uridine diphosphate-5′- glucuronosyltransferase 1A1 through cross talk with constitutive androstane receptor

Hisashi Masuyama, Hideki Nakatsukasa, Yuji Hiramatsu

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Hyperbilirubinemia remains a common condition in neonates. The constitutive androstane receptor (CAR) is an orphan nuclear receptor that has been shown to participate in the activation of the uridine diphosphate-5′- glucuronosyltransferase 1A1 (UGT1A1) gene, which plays an important role in bilirubin clearance. Oncostatin M (OSM), a member of the IL-6 family, is involved in the maturation of fetal hepatocytes. We have demonstrated that low OSM levels are a potential indicator of neonatal jaundice and the need for phototherapy. In this study we examined the effects of OSM on CAR-mediated signaling to investigate its potential role in neonatal jaundice via the CAR-UGT1A1 pathway. We observed that OSM positively augmented the CAR and UGT1A1 expressions and CAR-mediated signaling in vivo and in vitro, through cross talk between the nuclear CAR receptor and the plasma membrane OSM receptor, via the MAPK cascade. These data suggest that OSM might play a role in bilirubin metabolism via the CAR-UGT1A1 pathway.

Original languageEnglish
Pages (from-to)745-753
Number of pages9
JournalMolecular Endocrinology
Volume24
Issue number4
DOIs
Publication statusPublished - Apr 2010

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Oncostatin M
Glucuronosyltransferase
Uridine Diphosphate
Neonatal Jaundice
Bilirubin
Oncostatin M Receptors
Orphan Nuclear Receptors
Hyperbilirubinemia
Phototherapy
constitutive androstane receptor
Hepatocytes
Interleukin-6
Cell Membrane

ASJC Scopus subject areas

  • Molecular Biology
  • Endocrinology

Cite this

Effect of oncostatin M on uridine diphosphate-5′- glucuronosyltransferase 1A1 through cross talk with constitutive androstane receptor. / Masuyama, Hisashi; Nakatsukasa, Hideki; Hiramatsu, Yuji.

In: Molecular Endocrinology, Vol. 24, No. 4, 04.2010, p. 745-753.

Research output: Contribution to journalArticle

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