Intrinsic endothelial remodeling drives brain capillary repair
- Neuron. 2026 May 11:S0896-6273(26)00315-6. doi: 10.1016/j.neuron.2026.04.020.
- 1. Institute of Pharmacology and Toxicology, University of Zurich, 8057 Zürich, Switzerland; Neuroscience Center Zurich, University and ETH Zurich, 8057 Zürich, Switzerland.
- 2. Department of Chemistry, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA 19104, USA; Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
- 3. Departments of Neurology and Ophthalmology, Programs in Neuroscience and Immunology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
- 4. Institute of Pharmacology and Toxicology, University of Zurich, 8057 Zürich, Switzerland; Neuroscience Center Zurich, University and ETH Zurich, 8057 Zürich, Switzerland; Department of Neurology, University Hospital Zurich, 8091 Zürich, Switzerland.
- 5. Neuroscience Center Zurich, University and ETH Zurich, 8057 Zürich, Switzerland; Department of Neurology, University Hospital Zurich, 8091 Zürich, Switzerland.
- 6. Institute of Pharmacology and Toxicology, University of Zurich, 8057 Zürich, Switzerland; Neuroscience Center Zurich, University and ETH Zurich, 8057 Zürich, Switzerland. Electronic address: [email protected].
The brain's microvasculature is essential for oxygen and nutrient delivery; however, the mechanisms underlying cerebral capillary repair following injury remain largely elusive. Here, we identify an unrecognized mechanism through which brain capillary endothelial cells (ECs) autonomously promote capillary remodeling. Using longitudinal two-photon imaging in mice, we demonstrate that following focal endothelial injury and selective loss of a single EC, neighboring ECs extend their plasma membranes toward each Other, rapidly re-establishing capillary continuity and blood flow within 24-48 h. This repair process engages vascular endothelial growth factor receptor 2 (VEGFR2) signaling but occurs independently of perivascular or glial cell involvement. Finally, we reveal regional differences in repair efficacy, with hippocampal capillaries exhibiting a slower and less-efficient response compared with those in the cortex. These findings reveal an intrinsic mechanism that safeguards microvascular integrity and suggest that regional vulnerabilities in endothelial repair could shape brain resilience to injury and disease.
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