Runx2 protein stabilizes hypoxia-inducible factor-1α through competition with von Hippel-Lindau protein (pVHL) and stimulates angiogenesis in growth plate hypertrophic chondrocytes.
The regulation of hypoxia-inducible factor-1α (HIF-1α) during endochondral bone formation is not fully understood. Here, we investigated the cross-talk between HIF-1α and Runt-related transcription factor 2 (Runx2) in the growth plate. Runx2 caused the accumulation of HIF-1α protein in ATDC5 chondrocytes and HEK293 cells under normoxic conditions. Runx2 also increased ... the nuclear translocation of HIF-1α when coexpressed in HEK293 cells and interacted with HIF-1α at the oxygen-dependent degradation domain (ODDD). In addition, Runx2 competed with von Hippel-Lindau tumor suppressor protein by directly binding to ODDD-HIF-1α and significantly inhibited the ubiquitination of HIF-1α, even though Runx2 did not change the hydroxylation status of HIF-1α. Furthermore, overexpression of Runx2 resulted in the significant enhancement of vascular endothelial growth factor (VEGF) promoter reporter activity and protein secretion. Runx2 significantly increased angiogenic activity in human umbilical vein endothelial cells in vitro. In wild-type mice, HIF-1α and Runx2 were colocalized in hypertrophic chondrocytes in which the cluster of differentiation 31 (CD31) protein was expressed at embryonic day 15.5 (E15.5). In contrast, the expression of HIF-1α was markedly reduced in areas of CD31 expression in Runx2(-/-) mice. These results suggest that Runx2 stabilizes HIF-1α by binding to ODDD to block the interaction between von Hippel-Lindau protein and HIF-1α. In conclusion, Runx2, HIF-1α, and VEGF may regulate vascular angiogenesis spatially and temporally in the hypertrophic zone of the growth plate during endochondral bone formation.
Mesh Terms:
Active Transport, Cell Nucleus, Animals, Cell Nucleus, Chondrocytes, Core Binding Factor Alpha 1 Subunit, HEK293 Cells, Humans, Hydroxylation, Hypoxia-Inducible Factor 1, alpha Subunit, Mice, Mice, Knockout, Neovascularization, Physiologic, Protein Binding, Protein Stability, Protein Structure, Tertiary, Vascular Endothelial Growth Factor A, Von Hippel-Lindau Tumor Suppressor Protein
Active Transport, Cell Nucleus, Animals, Cell Nucleus, Chondrocytes, Core Binding Factor Alpha 1 Subunit, HEK293 Cells, Humans, Hydroxylation, Hypoxia-Inducible Factor 1, alpha Subunit, Mice, Mice, Knockout, Neovascularization, Physiologic, Protein Binding, Protein Stability, Protein Structure, Tertiary, Vascular Endothelial Growth Factor A, Von Hippel-Lindau Tumor Suppressor Protein
J. Biol. Chem.
Date: Apr. 27, 2012
PubMed ID: 22351759
View in: Pubmed Google Scholar
Download Curated Data For This Publication
142076
Switch View:
- Interactions 5