23 research outputs found

    A human homolog of the C. elegans polarity determinant Par-6 links Rac and Cdc42 to PKCĪ¶ signaling and cell transformation

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    AbstractBackground: Rac and Cdc42 are members of the Rho family of small GTPases. They modulate cell growth and polarity, and contribute to oncogenic transformation by Ras. The molecular mechanisms underlying these functions remain elusive, however.Results: We have identified a novel effector of Rac and Cdc42, hPar-6, which is the human homolog of a cell-polarity determinant in Caenorhabditis elegans. hPar-6 contains a PDZ domain and a Cdc42/Rac interactive binding (CRIB) motif, and interacts with Rac1 and Cdc42 in a GTP-dependent manner. hPar-6 also binds directly to an atypical protein kinase C isoform, PKCĪ¶ and forms a stable ternary complex with Rac1 or Cdc42 and PKCĪ¶. This association results in stimulation of PKCĪ¶ kinase activity. Moreover, hPar-6 potentiates cell transformation by Rac1/Cdc42 and its interaction with Rac1/Cdc42 is essential for this effect. Cell transformation by hPar-6 involves a PKCĪ¶-dependent pathway distinct from the pathway mediated by Raf.Conclusions: These findings indicate that Rac/Cdc42 can regulate cell growth through Par-6 and PKCĪ¶ and suggest that deregulation of cell-polarity signaling can lead to cell transformation

    R-spondin1 synergizes with Wnt3A in inducing osteoblast differentiation and osteoprotegerin expression

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    AbstractR-spondins are a new group of Wnt/Ī²-catenin signaling agonists, however, the role of these proteins in bone remains unclear. We reported herein that R-sponin1 (Rspo1) acted synergistically with Wnt3A to activate Wnt/Ī²-catenin signaling in the uncommitted mesenchymal C2C12 cells. Furthermore, we found that Rspo1 at concentrations as low as 10ng/ml synergized strongly with Wnt3A to induce C2C12 osteoblastic differentiation and osteoprotegerin expression. These events were blocked by Wnt/Ī²-catenin signaling antagonist Dickkopf-1. Finally, we demonstrated that Rspo1 synergized with Wnt3A to induce primary mouse osteoblast differentiation. Together, these findings suggest that Rpos1 may play an important role in bone remodeling
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