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TIE2 links MEKK3-KLF2/4 and PI3K signaling in cerebral cavernous malformation

Item Type:Article
Title:TIE2 links MEKK3-KLF2/4 and PI3K signaling in cerebral cavernous malformation
Creators Name:Li, Lun, Castro, Marco, Hongo, Hiroki, Ren, Jian, Shenkar, Robert, Jabarkheel, Rashad, Gao, Siqi, Narayan, Sweta, Frankfurter, Maxwell, Tang, Alan T., Yang, Jisheng, Chen, Mei, Bockman, Jenna, Mericko-Ishizuka, Patricia, Alcazar, Roberto, Sader, Georgio, Iqbal, Javed, Kinkade, Serena, Lightle, Rhonda, Ressler, Andrew K., Qu, Xianghu, Baldwin, H Scott, Marchuk, Douglas A., Awad, Issam A., Burkhardt, Jan-Karl, Potente, Michael and Kahn, Mark L.
Abstract:Cerebral cavernous malformations (CCMs) are vascular lesions in the central nervous system that can cause strokes and seizures. Aggressive CCM growth follows an endothelial cell two-hit mechanism in which enhanced MEKK3-KLF2/4 signaling stimulates PI3K signaling, but how these pathways are linked has been undefined. Here, we use human CCM specimens, two mouse models of CCM disease, and primary human endothelial cells to examine the roles of the major endothelial growth factor receptors, VEGFR2 and TIE2. We find no evidence of augmented VEGFR2 signaling in CCM lesions, and neither genetic nor pharmacologic blockade of VEGFR2 reduced CCM formation in mouse models. Instead, we observe markedly increased phospho-TIE2 levels in human and mouse CCM lesions, MEKK3-KLF2/4-driven induction of TIE2 receptor expression, and almost complete rescue of CCM formation following genetic or pharmacologic TIE2 blockade in mouse models. Our studies identify TIE2 as the molecular link between the MEKK3-KLF2/4 and PI3K signaling pathways during CCM formation and suggest that targeting TIE2 may be an effective means to treat human CCM disease.
Keywords:Animal Disease Models, Central Nervous System Cavernous Hemangioma, Endothelial Cells, Inbred C57BL Mice, Kruppel-Like Factor 4, Kruppel-Like Transcription Factors, MAP Kinase Kinase Kinase 3, Phosphatidylinositol 3-Kinases, Signal Transduction, TIE-2 Receptor, Vascular Endothelial Growth Factor Receptor-2, Animals, Mice
Source:Journal of Experimental Medicine
ISSN:0022-1007
Publisher:Rockefeller University Press
Volume:223
Number:5
Page Range:e20251374
Date:4 May 2026
Official Publication:https://doi.org/10.1084/jem.20251374
PubMed:View item in PubMed

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