Literature DB >> 29976569

SMAD4 Prevents Flow Induced Arteriovenous Malformations by Inhibiting Casein Kinase 2.

Roxana Ola1,2,3,4, Sandrine H Künzel1, Feng Zhang1, Gael Genet1, Raja Chakraborty1, Laurence Pibouin-Fragner5, Kathleen Martin1, William Sessa6, Alexandre Dubrac1, Anne Eichmann1,7,5.   

Abstract

BACKGROUND: Hereditary hemorrhagic telangiectasia (HHT) is an inherited vascular disorder that causes arteriovenous malformations (AVMs). Mutations in the genes encoding Endoglin ( ENG) and activin-receptor-like kinase 1 ( AVCRL1 encoding ALK1) cause HHT type 1 and 2, respectively. Mutations in the SMAD4 gene are present in families with juvenile polyposis-HHT syndrome that involves AVMs. SMAD4 is a downstream effector of transforming growth factor-β (TGFβ)/bone morphogenetic protein (BMP) family ligands that signal via activin-like kinase receptors (ALKs). Ligand-neutralizing antibodies or inducible, endothelial-specific Alk1 deletion induce AVMs in mouse models as a result of increased PI3K (phosphatidylinositol 3-kinase)/AKT (protein kinase B) signaling. Here we addressed if SMAD4 was required for BMP9-ALK1 effects on PI3K/AKT pathway activation.
METHODS: The authors generated tamoxifen-inducible, postnatal, endothelial-specific Smad4 mutant mice ( Smad4iΔEC).
RESULTS: We found that loss of endothelial Smad4 resulted in AVM formation and lethality. AVMs formed in regions with high blood flow in developing retinas and other tissues. Mechanistically, BMP9 signaling antagonized flow-induced AKT activation in an ALK1- and SMAD4-dependent manner. Smad4iΔEC endothelial cells in AVMs displayed increased PI3K/AKT signaling, and pharmacological PI3K inhibitors or endothelial Akt1 deletion both rescued AVM formation in Smad4iΔEC mice. BMP9-induced SMAD4 inhibited casein kinase 2 ( CK2) transcription, in turn limiting PTEN phosphorylation and AKT activation. Consequently, CK2 inhibition prevented AVM formation in Smad4iΔEC mice.
CONCLUSIONS: Our study reveals SMAD4 as an essential effector of BMP9-10/ALK1 signaling that affects AVM pathogenesis via regulation of CK2 expression and PI3K/AKT1 activation.

Entities:  

Keywords:  Telangiectasia, hereditary hemorrhagic; activin receptors, type II; arteriovenous malformations; casein kinase; phosphatidylinositol 3-kinase; proto-oncogene proteins c-akt

Mesh:

Substances:

Year:  2018        PMID: 29976569      PMCID: PMC6309254          DOI: 10.1161/CIRCULATIONAHA.118.033842

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  50 in total

1.  The tumor suppressor PTEN is phosphorylated by the protein kinase CK2 at its C terminus. Implications for PTEN stability to proteasome-mediated degradation.

Authors:  J Torres; R Pulido
Journal:  J Biol Chem       Date:  2001-01-12       Impact factor: 5.157

2.  Protein kinase CK2 phosphorylates and upregulates Akt/PKB.

Authors:  G Di Maira; M Salvi; G Arrigoni; O Marin; S Sarno; F Brustolon; L A Pinna; M Ruzzene
Journal:  Cell Death Differ       Date:  2005-06       Impact factor: 15.828

3.  Dll4 and Notch signalling couples sprouting angiogenesis and artery formation.

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Journal:  Nat Cell Biol       Date:  2017-07-17       Impact factor: 28.824

Review 4.  ALK1 signaling in development and disease: new paradigms.

Authors:  Beth L Roman; Andrew P Hinck
Journal:  Cell Mol Life Sci       Date:  2017-09-04       Impact factor: 9.261

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6.  Interaction between alk1 and blood flow in the development of arteriovenous malformations.

Authors:  Paola Corti; Sarah Young; Chia-Yuan Chen; Michael J Patrick; Elizabeth R Rochon; Kerem Pekkan; Beth L Roman
Journal:  Development       Date:  2011-03-09       Impact factor: 6.868

7.  Alk2/ACVR1 and Alk3/BMPR1A Provide Essential Function for Bone Morphogenetic Protein-Induced Retinal Angiogenesis.

Authors:  Heon-Woo Lee; Diana C Chong; Roxana Ola; William P Dunworth; Stryder Meadows; Jun Ka; Vesa M Kaartinen; Yibing Qyang; Ondine Cleaver; Victoria L Bautch; Anne Eichmann; Suk-Won Jin
Journal:  Arterioscler Thromb Vasc Biol       Date:  2017-02-23       Impact factor: 8.311

8.  Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.

Authors:  D W Johnson; J N Berg; M A Baldwin; C J Gallione; I Marondel; S J Yoon; T T Stenzel; M Speer; M A Pericak-Vance; A Diamond; A E Guttmacher; C E Jackson; L Attisano; R Kucherlapati; M E Porteous; D A Marchuk
Journal:  Nat Genet       Date:  1996-06       Impact factor: 38.330

9.  Defective fluid shear stress mechanotransduction mediates hereditary hemorrhagic telangiectasia.

Authors:  Nicolas Baeyens; Bruno Larrivée; Roxana Ola; Brielle Hayward-Piatkowskyi; Alexandre Dubrac; Billy Huang; Tyler D Ross; Brian G Coon; Elizabeth Min; Maya Tsarfati; Haibin Tong; Anne Eichmann; Martin A Schwartz
Journal:  J Cell Biol       Date:  2016-09-19       Impact factor: 10.539

10.  Proteus Syndrome with Arteriovenous Malformation.

Authors:  Ali Asilian; Atefeh Sadat Kamali; Nabet Tajmir Riahi; Neda Adibi; Fatemeh Mokhtari
Journal:  Adv Biomed Res       Date:  2017-03-07
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7.  Role of Venous Endothelial Cells in Developmental and Pathologic Angiogenesis.

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8.  Isolation of Highly Purified and Viable Retinal Endothelial Cells.

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9.  Overexpression of Activin Receptor-Like Kinase 1 in Endothelial Cells Suppresses Development of Arteriovenous Malformations in Mouse Models of Hereditary Hemorrhagic Telangiectasia.

Authors:  Yong Hwan Kim; Phuong-Nhung Vu; Se-Woon Choe; Chang-Jin Jeon; Helen M Arthur; Calvin P H Vary; Young Jae Lee; S Paul Oh
Journal:  Circ Res       Date:  2020-07-31       Impact factor: 17.367

10.  Defective Flow-Migration Coupling Causes Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia.

Authors:  Hyojin Park; Jessica Furtado; Mathilde Poulet; Minhwan Chung; Sanguk Yun; Sungwoon Lee; William C Sessa; Claudio A Franco; Martin A Schwartz; Anne Eichmann
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