Smad3-dependent nuclear translocation of β-catenin is required for TGF-β1-induced proliferation of bone marrow-derived adult human mesenchymal stem cells

H Jian, X Shen, I Liu, M Semenov, XI He… - Genes & …, 2006 - genesdev.cshlp.org
H Jian, X Shen, I Liu, M Semenov, XI He, XF Wang
Genes & development, 2006genesdev.cshlp.org
Adult mesenchymal stem cells (MSCs) derived from bone marrow contribute to the
regeneration of multiple types of mesenchymal tissues. Here we describe the functional role
of a novel form of cross-talk between the transforming growth factor β1 (TGF-β1) and Wnt
signaling pathways in regulating the activities of human MSCs. We show that TGF-β1
induces rapid nuclear translocation of β-catenin in MSCs in a Smad3-dependent manner.
Functionally, this pathway is required for the stimulation of MSC proliferation and the …
Adult mesenchymal stem cells (MSCs) derived from bone marrow contribute to the regeneration of multiple types of mesenchymal tissues. Here we describe the functional role of a novel form of cross-talk between the transforming growth factor β1 (TGF-β1) and Wnt signaling pathways in regulating the activities of human MSCs. We show that TGF-β1 induces rapid nuclear translocation of β-catenin in MSCs in a Smad3-dependent manner. Functionally, this pathway is required for the stimulation of MSC proliferation and the inhibition of MSC osteogenic differetiation by TGF-β1, likely through the regulation of specific downstream target genes. These results provide evidence for a new mode of cooperation between the TGF-β and Wnt signaling pathways in this specific cellular context and suggest a potentially important role for this distinct signaling pathway in the control of self-renewal and differentiation of a specific type of MSCs.
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