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

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.

Authors

Institutions

Publication Details

Journal
The Journal of Experimental Medicine
Published
2026-03-27
DOI
https://doi.org/10.1084/jem.20251374
Primary Topic
Vascular Malformations Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

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

Alan T. Tang, Rashad Jabarkheel, Mark L. Kahn, Andrew K. Ressler et al.
The Journal of Experimental Medicine
Vascular Malformations Diagnosis and Treatment
article

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

Alan T. Tang, Rashad Jabarkheel, Mark L. Kahn, Andrew K. Ressler, Michael Potente, Maxwell Frankfurter, Rhonda Lightle, Douglas A. Marchuk, Patricia Mericko-Ishizuka, Serena Kinkade, Jenna Bockman, Lun Li, Jisheng Yang, Georgio Sader, Roberto Alcazar, Siqi Gao, Mei Chen, Issam A. Awad, Sweta Narayan, Javed Iqbal, Marco Castro, Robert Shenkar, Jian Ren, Hiroki Hongo, Xianghu Qu, H. Scott Baldwin, Jan-Karl Burkhardt
article en

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.

The Journal of Experimental MedicineVol. 223(5)
Duke University (US), Capital Medical University (CN), Vanderbilt University (US), Max Delbrück Center (DE), Hospital of the University of Pennsylvania (US), University of Chicago (US), University of Tokyo Hospital (JP), Berlin Institute of Health at Charité - Universitätsmedizin Berlin (DE), The University of Tokyo (JP), University of Pennsylvania (US)
Openalex Percentile: Top 13%
Vascular Malformations Diagnosis and Treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.