Literature DB >> 32762495

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

Yong Hwan Kim1,2, Phuong-Nhung Vu3, Se-Woon Choe1,4, Chang-Jin Jeon5, Helen M Arthur6, Calvin P H Vary7, Young Jae Lee3, S Paul Oh1,2.   

Abstract

RATIONALE: Hereditary hemorrhagic telangiectasia (HHT) is a genetic disease caused by mutations in ENG, ALK1, or SMAD4. Since proteins from all 3 HHT genes are components of signal transduction of TGF-β (transforming growth factor β) family members, it has been hypothesized that HHT is a disease caused by defects in the ENG-ALK1-SMAD4 linear signaling. However, in vivo evidence supporting this hypothesis is scarce.
OBJECTIVE: We tested this hypothesis and investigated the therapeutic effects and potential risks of induced-ALK1 or -ENG overexpression (OE) for HHT. METHODS AND
RESULTS: We generated a novel mouse allele (ROSA26Alk1) in which HA (human influenza hemagglutinin)-tagged ALK1 and bicistronic eGFP expression are induced by Cre activity. We examined whether ALK1-OE using the ROSA26Alk1 allele could suppress the development of arteriovenous malformations (AVMs) in wounded adult skin and developing retinas of Alk1- and Eng-inducible knockout (iKO) mice. We also used a similar approach to investigate whether ENG-OE could rescue AVMs. Biochemical and immunofluorescence analyses confirmed the Cre-dependent OE of the ALK1-HA transgene. We could not detect any pathological signs in ALK1-OE mice up to 3 months after induction. ALK1-OE prevented the development of retinal AVMs and wound-induced skin AVMs in Eng-iKO as well as Alk1-iKO mice. ALK1-OE normalized expression of SMAD and NOTCH target genes in ENG-deficient endothelial cells (ECs) and restored the effect of BMP9 (bone morphogenetic protein 9) on suppression of phosphor-AKT levels in these endothelial cells. On the other hand, ENG-OE could not inhibit the AVM development in Alk1-iKO models.
CONCLUSIONS: These data support the notion that ENG and ALK1 form a linear signaling pathway for the formation of a proper arteriovenous network during angiogenesis. We suggest that ALK1 OE or activation can be an effective therapeutic strategy for HHT. Further research is required to study whether this therapy could be translated into treatment for humans.

Entities:  

Keywords:  activin receptor-like kinase 1; arteriovenous malformation; endoglin; endothelial cell; hereditary hemorrhagic telangiectasia; mice; signal transduction

Mesh:

Substances:

Year:  2020        PMID: 32762495      PMCID: PMC7554133          DOI: 10.1161/CIRCRESAHA.119.316267

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  69 in total

1.  Angiopoietin-2 Inhibition Rescues Arteriovenous Malformation in a Smad4 Hereditary Hemorrhagic Telangiectasia Mouse Model.

Authors:  Angela M Crist; Xingyan Zhou; Jone Garai; Amanda R Lee; Janina Thoele; Christoph Ullmer; Christian Klein; Jovanny Zabaleta; Stryder M Meadows
Journal:  Circulation       Date:  2019-04-23       Impact factor: 29.690

2.  Arteriovenous malformations in mice lacking activin receptor-like kinase-1.

Authors:  L D Urness; L K Sorensen; D Y Li
Journal:  Nat Genet       Date:  2000-11       Impact factor: 38.330

3.  Endoglin is required for myogenic differentiation potential of neural crest stem cells.

Authors:  Maria L Mancini; Joseph M Verdi; Barbara A Conley; Teodora Nicola; Douglas B Spicer; Leif H Oxburgh; Calvin P H Vary
Journal:  Dev Biol       Date:  2007-06-16       Impact factor: 3.582

4.  Alk1 controls arterial endothelial cell migration in lumenized vessels.

Authors:  Elizabeth R Rochon; Prahlad G Menon; Beth L Roman
Journal:  Development       Date:  2016-06-10       Impact factor: 6.868

5.  Real-time imaging of de novo arteriovenous malformation in a mouse model of hereditary hemorrhagic telangiectasia.

Authors:  Sung Ok Park; Mamta Wankhede; Young Jae Lee; Eun-Jung Choi; Naime Fliess; Se-Woon Choe; Seh-Hoon Oh; Glenn Walter; Mohan K Raizada; Brian S Sorg; S Paul Oh
Journal:  J Clin Invest       Date:  2009-10-01       Impact factor: 14.808

6.  A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4).

Authors:  Carol J Gallione; Gabriela M Repetto; Eric Legius; Anil K Rustgi; Susan L Schelley; Sabine Tejpar; Grant Mitchell; Eric Drouin; Cornelius J J Westermann; Douglas A Marchuk
Journal:  Lancet       Date:  2004-03-13       Impact factor: 79.321

7.  Pathogenesis of arteriovenous malformations in the absence of endoglin.

Authors:  Marwa Mahmoud; Kathleen R Allinson; Zhenhua Zhai; Rachael Oakenfull; Pranita Ghandi; Ralf H Adams; Marcus Fruttiger; Helen M Arthur
Journal:  Circ Res       Date:  2010-03-11       Impact factor: 17.367

8.  Endoglin prevents vascular malformation by regulating flow-induced cell migration and specification through VEGFR2 signalling.

Authors:  Yi Jin; Lars Muhl; Mikhail Burmakin; Yixin Wang; Anne-Claire Duchez; Christer Betsholtz; Helen M Arthur; Lars Jakobsson
Journal:  Nat Cell Biol       Date:  2017-05-22       Impact factor: 28.824

Review 9.  Endoglin as an Adhesion Molecule in Mature and Progenitor Endothelial Cells: A Function Beyond TGF-β.

Authors:  Elisa Rossi; Carmelo Bernabeu; David M Smadja
Journal:  Front Med (Lausanne)       Date:  2019-01-30

10.  Structural Basis of the Human Endoglin-BMP9 Interaction: Insights into BMP Signaling and HHT1.

Authors:  Takako Saito; Marcel Bokhove; Romina Croci; Sara Zamora-Caballero; Ling Han; Michelle Letarte; Daniele de Sanctis; Luca Jovine
Journal:  Cell Rep       Date:  2017-05-30       Impact factor: 9.423

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Journal:  Science       Date:  2022-03-04       Impact factor: 63.714

2.  Bone Marrow-Derived Alk1 Mutant Endothelial Cells and Clonally Expanded Somatic Alk1 Mutant Endothelial Cells Contribute to the Development of Brain Arteriovenous Malformations in Mice.

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Journal:  Transl Stroke Res       Date:  2021-10-21       Impact factor: 6.800

Review 3.  Vascular endothelial cell specification in health and disease.

Authors:  Corina Marziano; Gael Genet; Karen K Hirschi
Journal:  Angiogenesis       Date:  2021-04-12       Impact factor: 9.596

Review 4.  Hereditary Haemorrhagic Telangiectasia, an Inherited Vascular Disorder in Need of Improved Evidence-Based Pharmaceutical Interventions.

Authors:  Ryan O Snodgrass; Timothy J A Chico; Helen M Arthur
Journal:  Genes (Basel)       Date:  2021-01-27       Impact factor: 4.096

5.  MicroRNA-132-3p, Downregulated in Myeloid Angiogenic Cells from Hereditary Hemorrhagic Telangiectasia Patients, Is Enriched in the TGFβ and PI3K/AKT Signalling Pathways.

Authors:  Anthony Cannavicci; Qiuwang Zhang; Marie E Faughnan; Michael J B Kutryk
Journal:  Genes (Basel)       Date:  2022-04-09       Impact factor: 4.141

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Authors:  Helen M Arthur; Beth L Roman
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Journal:  Front Hum Neurosci       Date:  2022-09-21       Impact factor: 3.473

Review 8.  Review of treatment and therapeutic targets in brain arteriovenous malformation.

Authors:  Peipei Pan; Shantel Weinsheimer; Daniel Cooke; Ethan Winkler; Adib Abla; Helen Kim; Hua Su
Journal:  J Cereb Blood Flow Metab       Date:  2021-06-23       Impact factor: 6.960

9.  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
Journal:  Circulation       Date:  2021-06-29       Impact factor: 39.918

Review 10.  The versatility and paradox of BMP signaling in endothelial cell behaviors and blood vessel function.

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