| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Molecular Endocrinology, Vol 6, 935-942, Copyright © 1992 by Endocrine Society
ARTICLES |
L Bartalena, A Farsetti, IL Flink and J Robbins
Genetics and Biochemistry Branch, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892.
T4-binding globulin (TBG) shares a high degree of homology with two serpin antiproteases, alpha 1-antichymotrypsin (ACT) and alpha 1- antitrypsin (AT), whose synthesis is increased during the acute phase phenomenon, which accompanies trauma, infections, and neoplasms. Interleukin-6 (IL-6) is believed to be the main effector of the acute phase response. When evaluated in human hepatoblastoma-derived (Hep G2) cells exposed to different doses of the recombinant human cytokine for variable time intervals, IL-6 caused a dose- and time-dependent decrease in the secretion of [35S]methionine-labeled TBG, transthyretin (TTR), and albumin. The secretion of ACT and AT was increased. These changes were not due to alterations in the secretory process, since the kinetics of secretion of newly synthesized proteins were not modified. IL-6 did, however, cause a decrease in the steady state levels of mRNA for TTR, TBG, and albumin and an increase in ACT and AT mRNAs. In addition, nuclear run-off assay demonstrated a decrease in the transcription of TTR, TBG, and albumin genes and an increased transcription of the ACT gene. Quantitation of the results showed that changes in the secretion of proteins, in steady state mRNA levels, and in gene transcription were superimposable for each protein, indicating that IL-6 exerts its effect on thyroid hormone-binding proteins mostly at the transcriptional level and that TTR is the thyroid hormone- binding protein showing the most pronounced negative regulation by IL- 6. The opposite effect of IL-6 on TBG and the antiproteases, despite their structural homology, underscores gene divergence among these proteins.
This article has been cited by other articles:
![]() |
M. A. Fishel, G. S. Watson, T. J. Montine, Q. Wang, P. S. Green, J. J. Kulstad, D. G. Cook, E. R. Peskind, L. D. Baker, D. Goldgaber, et al. Hyperinsulinemia Provokes Synchronous Increases in Central Inflammation and {beta}-Amyloid in Normal Adults Arch Neurol, October 1, 2005; 62(10): 1539 - 1544. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Wang, E. Gjernes, and H. Prydz Factor VIIa Induces Tissue Factor-dependent Up-regulation of Interleukin-8 in a Human Keratinocyte Line J. Biol. Chem., June 21, 2002; 277(26): 23620 - 23626. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. M. Calvo, E. Jauniaux, B. Gulbis, M. Asuncion, C. Gervy, B. Contempre, and G. Morreale de Escobar Fetal Tissues Are Exposed to Biologically Relevant Free Thyroxine Concentrations during Early Phases of Development J. Clin. Endocrinol. Metab., April 1, 2002; 87(4): 1768 - 1777. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Zhang, J.-J. Jiao, B. R. Bhavnani, and S.-P. Tam Regulation of human apolipoprotein A-I gene expression by equine estrogens J. Lipid Res., November 1, 2001; 42(11): 1789 - 1800. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Citarella, A. Felici, M. Brouwer, J. Wagstaff, A. Fantoni, and C. E. Hack Interleukin-6 Downregulates Factor XII Production by Human Hepatoma Cell Line (HepG2) Blood, August 15, 1997; 90(4): 1501 - 1507. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Cuthbert, Z. Wang, X. Zhang, and S.-P. Tam Regulation of Human Apolipoprotein A-I Gene Expression by Gramoxone J. Biol. Chem., June 6, 1997; 272(23): 14954 - 14960. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Zhang, Z.-Q. Chen, Z. Wang, W. Mohan, and S.-P. Tam Protein-DNA Interactions at a Drug-responsive Element of the Human Apolipoprotein A-I Gene J. Biol. Chem., October 25, 1996; 271(43): 27152 - 27160. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |