RT Journal Article
SR Electronic
T1 Disruption of Bmal1 impairs blood—brain barrier integrity via pericyte dysfunction
JF The Journal of Neuroscience
JO J. Neurosci.
FD Society for Neuroscience
SP 3639-16
DO 10.1523/JNEUROSCI.3639-16.2017
A1 Ryota Nakazato
A1 Kenji Kawabe
A1 Daisuke Yamada
A1 Shinsuke Ikeno
A1 Michihiro Mieda
A1 Shigeki Shimba
A1 Eiichi Hinoi
A1 Yukio Yoneda
A1 Takeshi Takarada
YR 2017
UL http://www.jneurosci.org/content/early/2017/09/14/JNEUROSCI.3639-16.2017.abstract
AB Circadian rhythm disturbances are well-established in neurological diseases. However, how these disruptions cause homeostatic imbalances remains poorly understood. Brain and muscle aryl hydrocarbon receptor nuclear translocator-like protein 1 (Bmal1) is a major circadian clock transcriptional activator, and Bmal1 deficiency in male Bmal1nestin-/- mice induced marked astroglial activation without affecting the number of astrocytes in the brain and spinal cord. Bmal1 deletion caused blood—brain barrier (BBB) hyperpermeability with an age-dependent loss of pericyte coverage of blood vessels in the brain. Using Nestin-green fluorescent protein (GFP) transgenic mice, we determined that pericytes are Nestin-GFP+ in the adult brain. Bmal1 deletion caused Nestin-GFP+ pericyte dysfunction, including downregulation of platelet-derived growth factor receptor β (PDGFRβ), a protein necessary for maintaining BBB integrity. Knockdown of Bmal1 downregulated PDGFRβ transcription in the brain pericyte cell line. Thus, circadian clock component Bmal1 maintain BBB integrity via regulating pericytes.Significant StatementCircadian rhythm disturbances may play a role in neurodegenerative disorders, such as Alzheimer's disease. Our results revealed that one of the circadian clock component maintains the integrity of the blood—brain barrier (BBB) by regulating vascular-embedded pericytes. These cells were recently identified as a vital component for the control of BBB permeability and cerebral blood flow. Our present study demonstrates the involvement of circadian clock component Bmal1 in BBB homeostasis and highlights the role of Bmal1 dysfunction in multiple neurological diseases.