𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The osteogenic transcription factor Runx2 regulates components of the fibroblast growth factor/proteoglycan signaling axis in osteoblasts

✍ Scribed by Nadiya M. Teplyuk; Larisa M. Haupt; Ling Ling; Christian Dombrowski; Foong Kin Mun; Saminathan S. Nathan; Jane B. Lian; Janet L. Stein; Gary S. Stein; Simon M. Cool; Andre J. van Wijnen


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
406 KB
Volume
107
Category
Article
ISSN
0730-2312

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Heparan sulfate proteoglycans cooperate with basic fibroblast growth factor (bFGF/FGF2) signaling to control osteoblast growth and differentiation, as well as metabolic functions of osteoblasts. FGF2 signaling modulates the expression and activity of Runt‐related transcription factor 2 (Runx2/Cbfa1), a key regulator of osteoblast proliferation and maturation. Here, we have characterized novel Runx2 target genes in osteoprogenitors under conditions that promote growth arrest while not yet permitting sustained phenotypic maturation. Runx2 enhances expression of genes related to proteoglycan‐mediated signaling, including FGF receptors (e.g., FGFR2 and FGFR3) and proteoglycans (e.g., syndecans [Sdc1, Sdc2, Sdc3], glypicans [Gpc1], versican [Vcan]). Runx2 increases expression of the glycosyltransferase Exostosin‐1 (Ext1) and heparanase, as well as alters the relative expression of N‐linked sulfotransferases (Ndst1 = Ndst2 > Ndst3) and enzymes mediating O‐linked sulfation of heparan sulfate (Hs2st > Hs6st) or chondroitin sulfate (Cs4st > Cs6st). Runx2 cooperates with FGF2 to induce expression of Sdc4 and the sulfatase Galns, but Runx2 and FGF2 suppress Gpc6, thus suggesting intricate Runx2 and FGF2 dependent changes in proteoglycan utilization. One functional consequence of Runx2 mediated modulations in proteoglycan‐related gene expression is a change in the responsiveness of bone markers to FGF2 stimulation. Runx2 and FGF2 synergistically enhance osteopontin expression (>100 fold), while FGF2 blocks Runx2 induction of alkaline phosphatase. Our data suggest that Runx2 and the FGF/proteoglycan axis may form an extracellular matrix (ECM)‐related regulatory feed‐back loop that controls osteoblast proliferation and execution of the osteogenic program. J. Cell. Biochem. 107: 144–154, 2009. © 2009 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Regulation of the osteoblast-specific tr
✍ Renny T. Franceschi; Guozhi Xiao 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 146 KB

## Abstract The Cbfa1/Runx2 is an important transcription factor necessary for osteoblast differentiation and bone formation. However, the signaling pathways regulating Runx2 activity are just beginning to be understood. Inconsistencies between Runx2 mRNA or protein levels and its transcriptional a

Expression and regulation of the insulin
✍ Ruslan Novosyadlyy; Kyrylo Tron; Jozsef Dudas; Giuliano Ramadori; Jens-Gerd Scha 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 309 KB

## Abstract Apart from hepatic stellate cells (HSC), liver myofibroblasts (MF) represent a second mesenchymal cell population involved in hepatic fibrogenesis. The IGF system including the insulin‐like growth factors I and II (IGF‐I, ‐II), their receptors (IGF‐I receptor, IGF‐IR; IGF‐II/mannose 6‐p

Altered transcriptional regulation of th
✍ Kosaku Uchida; Masashi Kondo; Shin Takeda; Hirotaka Osada; Toshitada Takahashi; 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 158 KB 👁 2 views

The insulin-like growth factor 2 (IGF2) gene is regulated in a complex manner, involving developmentally regulated use of four different promoters as well as transcriptional repression of the maternal allele due to genomic imprinting. It has been well documented that liver is an exceptional organ in

Characterization of the promoter for the
✍ Michael L. Gagnon; Grace K. Moy; Michael Klagsbrun 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 295 KB 👁 2 views

Human lymphoid cells were found to synthesize predominantly antisense, and not sense, fibroblast growth factor-2 (FGF-2) mRNA. Two cDNAs corresponding to human 1069- and 1173-nucleotide antisense FGF-2 mRNAs were cloned from Jurkat T cells. The two cDNAs each possess a unique exon 1 and common exon

PI3K/Akt-dependent regulation of the tra
✍ M. Wiedmann; X. Wang; X. Tang; M. Han; M. Li; Z. Mao 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 270 KB

## Abstract Survival signals such as insulin‐like growth factor‐1 (IGF‐1) or membrane depolarization convey their neuronal protective effects through the activation of signaling networks and nuclear factors. In cerebellar granule neurons, IGF‐1 mediates survival primarily through the PI3K/Akt pathw