Sensory-Related Neural Activity Regulates the Structure of Vascular Networks in the Cerebral Cortex
Open accessAbstract
Neurovascular interactions are essential for proper brain function. While the effect of neural activity on cerebral blood flow has been extensively studied, whether or not neural activity influences vascular patterning remains elusive. Here, we demonstrate that neural activity promotes the formation of vascular networks in the early postnatal mouse barrel cortex. Using a combination of genetics, imaging, and computational tools to allow simultaneous analysis of neuronal and vascular components, we found that vascular density and branching were decreased in the barrel cortex when sensory input was reduced by either a complete deafferentation, a genetic impairment of neurotransmitter release at thalamocortical synapses, or a selective reduction of sensory-related neural activity by whisker plucking. In contrast, enhancement of neural activity by whisker stimulation led to an increase in vascular density and branching. The finding that neural activity is necessary and sufficient to trigger alterations of vascular networks reveals an important feature of neurovascular interactions.
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Deprivation of sensory input in the mouse barrel cortex by either surgical deafferentation or genetic inhibition of neurotransmitter release results in postnatal reduction in vascular density, suggesting that neuronal activity remains an important regulator of vascular plasticity after birth.
“Deprivation of sensory input in the mouse barrel cortex by either surgical deafferentation or genetic inhibition of neurotransmitter release results in postnatal reduction in vascular density (340), suggesting that neuronal activity remains an important regulator of vascular plasticity after birth.”
From Blood-Brain Barrier: From Physiology to Disease and Back (2019) · cites this paper as [340]
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- Authors
- Lacoste, B., Comin, C. H., Ben-Zvi, A., Kaeser, P. S., Xu, X., Costa, L. D. F., & Gu, C.
- Affiliations
- Harvard University (US)
- Universidade de São Paulo (BR)
- Brigham and Women's Hospital (US)
- Corresponding author
- Gu, Chenghua
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2014-09
- Volume
- 83
- Issue
- 5
- Pages
- 1117-1130
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC4166422
- OpenAlex
- W2014932510
- Cited by
- 171
- References
- 6
- Citations by year
- 2026: 11 · 2025: 17 · 2024: 12 · 2023: 20 · 2022: 23 · 2021: 25 · 2020: 16 · 2019: 8 · 2018: 7 · 2017: 12 · 2016: 10 · 2015: 8 · 2014: 2
- FWCI
- 5.55
- Type
- journal article
- Language
- en
- Open access
- bronze
- dx.doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Scientific Electronic Library Online (São Paulo Research Foundation, Latin American and Caribbean Center on Health Sciences Information, Conselho Nacional de Desenvolvimento Científico e Tecnológico) (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Drug Abuse (K01DA029044)
- National Institute of Neurological Disorders and Stroke (R01NS064583, P30NS072030)
- Topics
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
- Keywords
- neurovascular interactions, cerebral blood flow, vascular network formation, barrel cortex, sensory input, deafferentation, thalamocortical synapses, neurotransmitter release, whisker stimulation, vessel density, vascular branching, postnatal development, mice
- MeSH terms
- Afferent Pathways, Age Factors, Animals, Animals, Newborn, Cerebral Cortex, Cerebrovascular Circulation, Luminescent Proteins, Mice, Transgenic, Phosphopyruvate Hydratase, Physical Stimulation, Sensory Receptor Cells, Vibrissae, Gene Expression Regulation, Developmental, GTP-Binding Proteins, rab3 GTP-Binding Proteins, Receptor, TIE-2, Cell Proliferation, Mice, In Vitro Techniques
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