PMID- 25845934 OWN - NLM STAT- MEDLINE DCOM- 20151006 LR - 20161125 IS - 1879-1220 (Electronic) IS - 0960-0760 (Linking) VI - 152 DP - 2015 Aug TI - A review of 1alpha,25(OH)2D3 dependent Pdia3 receptor complex components in Wnt5a non-canonical pathway signaling. PG - 84-8 LID - S0960-0760(15)00099-0 [pii] LID - 10.1016/j.jsbmb.2015.04.002 [doi] AB - Wnt5a and 1alpha,25-dihydroxyvitamin D3 [1alpha,25(OH)2D3] regulate endochondral ossification. 1alpha,25(OH)2D3 initiates its calcium-dependent effects via its membrane-associated receptor, protein disulfide isomerase A3 (Pdia3). 1alpha,25(OH)2D3 binding to Pdia3 triggers the interaction between Pdia3 and phospholipase A2 (PLA2)-activating protein (PLAA), resulting in downstream activation of calcium/calmodulin-dependent protein kinase II (CaMKII), PLA2, and protein kinase C (PKC). Wnt5a initiates its calcium-dependent effects via binding its receptors Frizzled2 (FZD2) and Frizzled5 (FZD5) and receptor tyrosine kinase-like orphan receptor 2 (ROR2), activating intracellular calcium release and stimulating PKC and CaMKII. Recent efforts to determine the inter-relation between Wnt5a and 1alpha,25(OH)2D3 signaling pathways have demonstrated that Wnt5a signals through a CaMKII/PLA2/PGE2/PKC cascade in chondrocytes and osteoblasts in which the components of the Pdia3 receptor complex were required. Furthermore, ROR2, but not FZD2 or FZD5, was required to mediate the calcium-dependent actions of 1alpha,25(OH)2D3. This review provides evidence that 1alpha,25(OH)2D3 and Wnt5a mediate their calcium-dependent pathways via similar receptor components and proposes that these pathways may interact since they are competing for the same receptor complex components. CI - Copyright (c) 2015 Elsevier Ltd. All rights reserved. FAU - Doroudi, Maryam AU - Doroudi M AD - School of Biology, Georgia Institute of Technology, Atlanta, GA 30332, USA. FAU - Olivares-Navarrete, Rene AU - Olivares-Navarrete R AD - Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA 23284, USA. FAU - Boyan, Barbara D AU - Boyan BD AD - School of Biology, Georgia Institute of Technology, Atlanta, GA 30332, USA; Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA 23284, USA; Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA. Electronic address: bboyan@vcu.edu. FAU - Schwartz, Zvi AU - Schwartz Z AD - Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA 23284, USA; Department of Periodontics, The University of Texas Health Science Center at San Antonio, San Antonio, TX 78284, USA. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Review DEP - 20150403 PL - England TA - J Steroid Biochem Mol Biol JT - The Journal of steroid biochemistry and molecular biology JID - 9015483 RN - 0 (Frizzled Receptors) RN - 0 (Fzd2 protein, mouse) RN - 0 (Fzd5 protein, mouse) RN - 0 (Proteins) RN - 0 (Wnt Proteins) RN - 0 (Wnt-5a Protein) RN - 0 (Wnt5a protein, mouse) RN - 0 (phospholipase A2-activating protein) RN - EC 2.7.10.1 (Receptor Tyrosine Kinase-like Orphan Receptors) RN - EC 2.7.10.1 (Ror2 protein, mouse) RN - EC 2.7.11.13 (Protein Kinase C) RN - EC 2.7.11.17 (Calcium-Calmodulin-Dependent Protein Kinase Type 2) RN - EC 5.3.4.1 (Pdia3 protein, mouse) RN - EC 5.3.4.1 (Protein Disulfide-Isomerases) RN - FXC9231JVH (Calcitriol) SB - IM MH - Animals MH - Calcitriol/*metabolism MH - Calcium-Calmodulin-Dependent Protein Kinase Type 2/metabolism MH - Cell Line MH - Frizzled Receptors/metabolism MH - Humans MH - Mice MH - Protein Disulfide-Isomerases/*metabolism MH - Protein Kinase C/metabolism MH - Proteins/metabolism MH - Receptor Tyrosine Kinase-like Orphan Receptors/metabolism MH - Wnt Proteins/*metabolism MH - Wnt Signaling Pathway/*physiology MH - Wnt-5a Protein OTO - NOTNLM OT - 1,25-Dihydroxyvitamin D3 OT - Calmodulin OT - Phospholipase A2 activating protein OT - Protein disulfide isomerase A3 OT - Protein kinase C OT - Wnt5a EDAT- 2015/04/08 06:00 MHDA- 2015/10/07 06:00 CRDT- 2015/04/08 06:00 PHST- 2014/09/12 00:00 [received] PHST- 2015/03/16 00:00 [revised] PHST- 2015/04/02 00:00 [accepted] PHST- 2015/04/08 06:00 [entrez] PHST- 2015/04/08 06:00 [pubmed] PHST- 2015/10/07 06:00 [medline] AID - S0960-0760(15)00099-0 [pii] AID - 10.1016/j.jsbmb.2015.04.002 [doi] PST - ppublish SO - J Steroid Biochem Mol Biol. 2015 Aug;152:84-8. doi: 10.1016/j.jsbmb.2015.04.002. Epub 2015 Apr 3.