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WNT-3A-induced β-catenin signaling does not require signaling through heterotrimeric G proteins.

Authors :
Bowin CF
Inoue A
Schulte G
Source :
The Journal of biological chemistry [J Biol Chem] 2019 Aug 02; Vol. 294 (31), pp. 11677-11684. Date of Electronic Publication: 2019 Jun 24.
Publication Year :
2019

Abstract

The network of Wingless/Int-1 (WNT)-induced signaling pathways includes β-catenin-dependent and -independent pathways. β-Catenin regulates T cell factor/lymphoid enhancer-binding factor (TCF/LEF)-mediated gene transcription, and in response to WNTs, β-catenin signaling is initiated through engagement of a Frizzled (FZD)/LDL receptor-related protein 5/6 (LRP5/6) receptor complex. FZDs are G protein-coupled receptors, but the question of whether heterotrimeric G proteins are involved in WNT/β-catenin signaling remains unanswered. Here, we investigate whether acute activation of WNT/β-catenin signaling by purified WNT-3A requires functional signaling through heterotrimeric G proteins. Using genome editing, we ablated expression of G <subscript>s</subscript> /G <subscript>olf</subscript> /G <subscript>q</subscript> /G <subscript>11</subscript> /G <subscript>12</subscript> /G <subscript>13</subscript> /G <subscript>z</subscript> in HEK293 (ΔG7) cells, leaving the expression of pertussis toxin (PTX)-sensitive G <subscript>i/o</subscript> proteins unchanged, to assess whether WNT-3A activates WNT/β-catenin signaling in WT and ΔG7 cells devoid of functional G protein signaling. We monitored WNT-3A-induced activation by detection of phosphorylation of LDL receptor-related protein 6 (LRP6), electrophoretic mobility shift of the phosphoprotein Dishevelled (DVL), β-catenin stabilization and dephosphorylation, and TCF-dependent transcription. We found that purified, recombinant WNT-3A efficiently induces WNT/β-catenin signaling in ΔG7 cells in both the absence and presence of G <subscript>i/o</subscript> -blocking PTX. Furthermore, cells completely devoid of G protein expression, so called Gα-depleted HEK293 cells, maintain responsiveness to WNT-3A with regard to the hallmarks of WNT/β-catenin signaling. These findings corroborate the concept that heterotrimeric G proteins are not required for this FZD- and DVL-mediated signaling branch. Our observations agree with previous results arguing for FZD conformation-dependent functional selectivity between DVL and heterotrimeric G proteins. In conclusion, WNT/β-catenin signaling through FZDs does not require the involvement of heterotrimeric G proteins.<br /> (© 2019 Bowin et al.)

Details

Language :
English
ISSN :
1083-351X
Volume :
294
Issue :
31
Database :
MEDLINE
Journal :
The Journal of biological chemistry
Publication Type :
Academic Journal
Accession number :
31235524
Full Text :
https://doi.org/10.1074/jbc.AC119.009412