KLF4 is a key determinant in the development and progression of cerebral cavernous malformations
2016 (English)In: EMBO Molecular Medicine, ISSN 1757-4676, E-ISSN 1757-4684, Vol. 8, no 1, 6-24 p.Article in journal (Refereed) PublishedText
Cerebral cavernous malformations (CCMs) are vascular malformations located within the central nervous system often resulting in cerebral hemorrhage. Pharmacological treatment is needed, since current therapy is limited to neurosurgery. Familial CCM is caused by loss-of-function mutations in any of Ccm1, Ccm2, and Ccm3 genes. CCM cavernomas are lined by endothelial cells (ECs) undergoing endothelial-to-mesenchymal transition (EndMT). This switch in phenotype is due to the activation of the transforming growth factor beta/bone morphogenetic protein (TGFb/BMP) signaling. However, the mechanism linking Ccm gene inactivation and TGFb/ BMP-dependent EndMT remains undefined. Here, we report that Ccm1 ablation leads to the activation of a MEKK3-MEK5-ERK5MEF2 signaling axis that induces a strong increase in Kruppel-like factor 4 (KLF4) in ECs in vivo. KLF4 transcriptional activity is responsible for the EndMT occurring in CCM1-null ECs. KLF4 promotes TGFb/BMP signaling through the production of BMP6. Importantly, in endothelial-specific Ccm1 and Klf4 double knockout mice, we observe a strong reduction in the development of CCM and mouse mortality. Our data unveil KLF4 as a therapeutic target for CCM.
Place, publisher, year, edition, pages
2016. Vol. 8, no 1, 6-24 p.
CCM, EndMT, endothelial cells, KLF4, TGF beta-BMP
IdentifiersURN: urn:nbn:se:uu:diva-276831DOI: 10.15252/emmm.201505433ISI: 000368135800003PubMedID: 26612856OAI: oai:DiVA.org:uu-276831DiVA: diva2:903477
FunderEU, European Research Council, 268870EU, European Research Council, ITN VESSEL 317250EU, European Research Council, ENDOSTEM-HEALTH-2009-241440
De två första författarna delar förstaförfattarskapet2016-02-162016-02-162016-02-16Bibliographically approved