Literature DB >> 29449337

ALK1 Loss Results in Vascular Hyperplasia in Mice and Humans Through PI3K Activation.

Elisenda Alsina-Sanchís1,2, Yaiza García-Ibáñez1,2, Ana M Figueiredo1,3,2, Carla Riera-Domingo1,2, Agnès Figueras1,2, Xavier Matias-Guiu2,4,5,6, Oriol Casanovas1,2, Luisa M Botella7, Miquel A Pujana1,2, Antoni Riera-Mestre8,9, Mariona Graupera10,3,11, Francesc Viñals10,2,12.   

Abstract

OBJECTIVE: ALK1 (activin-receptor like kinase 1) is an endothelial cell-restricted receptor with high affinity for BMP (bone morphogenetic protein) 9 TGF-β (transforming growth factor-β) family member. Loss-of-function mutations in ALK1 cause a subtype of hereditary hemorrhagic telangiectasia-a rare disease characterized by vasculature malformations. Therapeutic strategies are aimed at reducing potential complications because of vascular malformations, but currently, there is no curative treatment for hereditary hemorrhagic telangiectasia. APPROACH AND
RESULTS: In this work, we report that a reduction in ALK1 gene dosage (heterozygous ALK1+/- mice) results in enhanced retinal endothelial cell proliferation and vascular hyperplasia at the sprouting front. We found that BMP9/ALK1 represses VEGF (vascular endothelial growth factor)-mediated PI3K (phosphatidylinositol 3-kinase) by promoting the activity of the PTEN (phosphatase and tensin homolog). Consequently, loss of ALK1 function in endothelial cells results in increased activity of the PI3K pathway. These results were confirmed in cutaneous telangiectasia biopsies of patients with hereditary hemorrhagic telangiectasia 2, in which we also detected an increase in endothelial cell proliferation linked to an increase on the PI3K pathway. In mice, genetic and pharmacological inhibition of PI3K is sufficient to abolish the vascular hyperplasia of ALK1+/- retinas and in turn normalize the vasculature.
CONCLUSIONS: Overall, our results indicate that the BMP9/ALK1 hub critically mediates vascular quiescence by limiting PI3K signaling and suggest that PI3K inhibitors could be used as novel therapeutic agents to treat hereditary hemorrhagic telangiectasia.
© 2018 American Heart Association, Inc.

Entities:  

Keywords:  endothelium; humans; mice; rare diseases; retina; telangiectasia, hereditary hemorrhagic

Mesh:

Substances:

Year:  2018        PMID: 29449337     DOI: 10.1161/ATVBAHA.118.310760

Source DB:  PubMed          Journal:  Arterioscler Thromb Vasc Biol        ISSN: 1079-5642            Impact factor:   8.311


  28 in total

1.  Shaping Waves of Bone Morphogenetic Protein Inhibition During Vascular Growth.

Authors:  Pierre J Guihard; Yina Guo; Xiuju Wu; Lily Zhang; Jiayi Yao; Medet Jumabay; Yucheng Yao; Alan Garfinkel; Kristina I Boström
Journal:  Circ Res       Date:  2020-08-28       Impact factor: 17.367

2.  Correcting Smad1/5/8, mTOR, and VEGFR2 treats pathology in hereditary hemorrhagic telangiectasia models.

Authors:  Santiago Ruiz; Haitian Zhao; Pallavi Chandakkar; Julien Papoin; Hyunwoo Choi; Aya Nomura-Kitabayashi; Radhika Patel; Matthew Gillen; Li Diao; Prodyot K Chatterjee; Mingzhu He; Yousef Al-Abed; Ping Wang; Christine N Metz; S Paul Oh; Lionel Blanc; Fabien Campagne; Philippe Marambaud
Journal:  J Clin Invest       Date:  2020-02-03       Impact factor: 14.808

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

Authors:  Roxana Ola; Sandrine H Künzel; Feng Zhang; Gael Genet; Raja Chakraborty; Laurence Pibouin-Fragner; Kathleen Martin; William Sessa; Alexandre Dubrac; Anne Eichmann
Journal:  Circulation       Date:  2018-11-20       Impact factor: 29.690

4.  The onset of PI3K-related vascular malformations occurs during angiogenesis and is prevented by the AKT inhibitor miransertib.

Authors:  Piotr Kobialka; Helena Sabata; Sandra D Castillo; Mariona Graupera; Odena Vilalta; Leonor Gouveia; Ana Angulo-Urarte; Laia Muixí; Jasmina Zanoncello; Oscar Muñoz-Aznar; Nagore G Olaciregui; Lucia Fanlo; Anna Esteve-Codina; Cinzia Lavarino; Biola M Javierre; Veronica Celis; Carlota Rovira; Susana López-Fernández; Eulàlia Baselga; Jaume Mora
Journal:  EMBO Mol Med       Date:  2022-06-13       Impact factor: 14.260

Review 5.  Annual Report on Sex in Preclinical Studies: Arteriosclerosis, Thrombosis, and Vascular Biology Publications in 2018.

Authors:  Hong S Lu; Ann Marie Schmidt; Robert A Hegele; Nigel Mackman; Daniel J Rader; Christian Weber; Alan Daugherty
Journal:  Arterioscler Thromb Vasc Biol       Date:  2019-12-23       Impact factor: 8.311

6.  KEA3: improved kinase enrichment analysis via data integration.

Authors:  Maxim V Kuleshov; Zhuorui Xie; Alexandra B K London; Janice Yang; John Erol Evangelista; Alexander Lachmann; Ingrid Shu; Denis Torre; Avi Ma'ayan
Journal:  Nucleic Acids Res       Date:  2021-07-02       Impact factor: 16.971

7.  Endoglin deficiency impairs VEGFR2 but not FGFR1 or TIE2 activation and alters VEGF-mediated cellular responses in human primary endothelial cells.

Authors:  Qiuwang Zhang; Chenxi Wang; Anthony Cannavicci; Marie E Faughnan; Michael J B Kutryk
Journal:  Transl Res       Date:  2021-04-22       Impact factor: 10.171

8.  Natural history of patients with venous thromboembolism and hereditary hemorrhagic telangiectasia. Findings from the RIETE registry.

Authors:  Antoni Riera-Mestre; José María Mora-Luján; Javier Trujillo-Santos; Jorge Del Toro; José Antonio Nieto; José María Pedrajas; Raquel López-Reyes; Silvia Soler; Aitor Ballaz; Pau Cerdà; Manel Monreal
Journal:  Orphanet J Rare Dis       Date:  2019-08-09       Impact factor: 4.123

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

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