Abstract
The enzyme PORCN is considered essential for Wnt secretion and signaling. However, PORCN inhibition did not phenocopy the effects of WNT4 knockdown in WNT4-dependent breast cancer cells, suggesting an atypical role for PORCN in WNT4 signaling. WNT4 or WNT3A were over-expressed in cell lines (breast and ovarian cancer, and fibrosarcoma). Conditioned medium from these cell lines, and co-culture systems, were used to assess Wnt secretion and activity. The dependence of Wnt secretion on PORCN and WLS was also tested. We observed that WLS was universally required for Wnt secretion and paracrine signaling. In contrast, the dependence of WNT3A secretion and activity on PORCN varied across cell lines, and WNT4 secretion was PORCN-independent in all models. Surprisingly, WNT4 did not present paracrine activity in any tested context. Absent the expected paracrine activity of secreted WNT4, we identified cell autonomous Wnt signaling activation by WNT4 and WNT3A, independent of PORCN and secretion. Direct transfection of Wnt protein activated the Wnt second messenger proteins DVL2 and DVL3, independent of activation of membrane receptors. The PORCN-independent, cell-autonomous Wnt signaling demonstrated herein may be critical in WNT4-driven cellular contexts, or those which are otherwise considered to have dysfunctional Wnt signaling.
Summary Statement Wnt proteins can mediate an atypical mode of cell-autonomous signaling, distinct from paracrine signaling, that is independent of both palmitoylation by PORCN and Wnt secretion.
List of Abbreviations
- AP
- Alkaline Phosphatase
- AXIN2
- Axin related protein 2
- CDH1
- E-cadherin
- CM
- Conditioned Media
- DVL
- Disheveled
- Fulv
- Fulvestrant
- FZD
- Frizzled
- ILC
- Invasive Lobular Carcinoma
- LRP
- Lipoprotein receptor-related protein
- PKO
- Porcupine knockout
- PORCN
- O-acyltransferase Porcupine
- PORCNi
- Porcupine inhibitor
- rWNT
- Recombinant WNT
- sWNT
- Secreted WNT
- WLS
- Wntless
- WNT
- Wingless/Integrated