Literature DB >> 32640906

Mural Cell-Specific Deletion of Cerebral Cavernous Malformation 3 in the Brain Induces Cerebral Cavernous Malformations.

Kang Wang1, Haifeng Zhang1, Yun He1, Quan Jiang1, Yoshiaki Tanaka2, In-Hyun Park2, Jordan S Pober1, Wang Min1, Huanjiao Jenny Zhou1.   

Abstract

OBJECTIVE: Cerebral cavernous malformations (CCM), consisting of dilated capillary channels formed by a single layer of endothelial cells lacking surrounding mural cells. It is unclear why CCM lesions are primarily confined to brain vasculature, although the 3 CCM-associated genes (CCM1, CCM2, and CCM3) are ubiquitously expressed in all tissues. We aimed to determine the role of CCM gene in brain mural cell in CCM pathogenesis. Approach and
Results: SM22α-Cre was used to drive a specific deletion of Ccm3 in mural cells, including pericytes and smooth muscle cells (Ccm3smKO). Ccm3smKO mice developed CCM lesions in the brain with onset at neonatal stages. One-third of Ccm3smKO mice survived upto 6 weeks of age, exhibiting seizures, and severe brain hemorrhage. The early CCM lesions in Ccm3smKO neonates were loosely wrapped by mural cells, and adult Ccm3smKO mice had clustered and enlarged capillary channels (caverns) formed by a single layer of endothelium lacking mural cell coverage. Importantly, CCM lesions throughout the entire brain in Ccm3smKO mice, which more accurately mimicked human disease than the current endothelial cell-specific CCM3 deletion models. Mechanistically, CCM3 loss in brain pericytes dramatically increased paxillin stability and focal adhesion formation, enhancing ITG-β1 (integrin β1) activity and extracellular matrix adhesion but reducing cell migration and endothelial cell-pericyte associations. Moreover, CCM3-wild type, but not a paxillin-binding defective mutant, rescued the phenotypes in CCM3-deficient pericytes.
CONCLUSIONS: Our data demonstrate for the first time that deletion of a CCM gene in the brain mural cell induces CCM pathogenesis.

Entities:  

Keywords:  cell adhesion; endothelial cells; muscle cells; paxillin; pericytes

Year:  2020        PMID: 32640906     DOI: 10.1161/ATVBAHA.120.314586

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


  6 in total

1.  CCM3 Loss-Induced Lymphatic Defect Is Mediated by the Augmented VEGFR3-ERK1/2 Signaling.

Authors:  Lingfeng Qin; Haifeng Zhang; Busu Li; Quan Jiang; Francesc Lopez; Wang Min; Jenny Huanjiao Zhou
Journal:  Arterioscler Thromb Vasc Biol       Date:  2021-10-21       Impact factor: 8.311

2.  Somatic PIK3CA Mutations in Sporadic Cerebral Cavernous Malformations.

Authors:  Matthieu Peyre; Danielle Miyagishima; Franck Bielle; Françoise Chapon; Michael Sierant; Quitterie Venot; Julie Lerond; Pauline Marijon; Samiya Abi-Jaoude; Tuan Le Van; Karim Labreche; Richard Houlston; Maxime Faisant; Stéphane Clémenceau; Anne-Laure Boch; Aurelien Nouet; Alexandre Carpentier; Julien Boetto; Angeliki Louvi; Michel Kalamarides
Journal:  N Engl J Med       Date:  2021-09-09       Impact factor: 91.245

Review 3.  Cerebral Cavernous Malformation Pathogenesis: Investigating Lesion Formation and Progression with Animal Models.

Authors:  Chelsea M Phillips; Svetlana M Stamatovic; Richard F Keep; Anuska V Andjelkovic
Journal:  Int J Mol Sci       Date:  2022-04-30       Impact factor: 6.208

4.  Contact-dependent signaling triggers tumor-like proliferation of CCM3 knockout endothelial cells in co-culture with wild-type cells.

Authors:  Matthias Rath; Konrad Schwefel; Matteo Malinverno; Dariush Skowronek; Alexandra Leopoldi; Robin A Pilz; Doreen Biedenweg; Sander Bekeschus; Josef M Penninger; Elisabetta Dejana; Ute Felbor
Journal:  Cell Mol Life Sci       Date:  2022-06-04       Impact factor: 9.207

5.  Caveolae-mediated Tie2 signaling contributes to CCM pathogenesis in a brain endothelial cell-specific Pdcd10-deficient mouse model.

Authors:  Lingfeng Qin; Quan Jiang; Katie N Murray; Haifeng Zhang; Huanjiao Jenny Zhou; Busu Li; Qun Lin; Morven Graham; Xinran Liu; Jaime Grutzendler; Wang Min
Journal:  Nat Commun       Date:  2021-01-25       Impact factor: 14.919

6.  Next-Generation Sequencing Advances the Genetic Diagnosis of Cerebral Cavernous Malformation (CCM).

Authors:  Valerio Benedetti; Rosalia Canzoneri; Andrea Perrelli; Carlo Arduino; Andrea Zonta; Alfredo Brusco; Saverio Francesco Retta
Journal:  Antioxidants (Basel)       Date:  2022-06-29
  6 in total

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