The blood-brain barrier (BBB) assures brain homeostasis through the specialized function of brain endothelial cells (BECs). Dysfunction of the BBB due to inflammatory processes is associated with several neurological disorders, including multiple sclerosis (MS). Understanding the mechanisms that underlie these processes may ultimately lead to new therapeutic strategies to restore BBB function, thereby fighting disease progression. In this study, we demonstrate for the first time a critical role of the Notch signaling pathway in the function of the BBB under resting and inflammatory conditions. Inhibition of the Notch signaling, either by a γ-secretase inhibitor or by genetic ablation of endothelial NOTCH, led to BBB dysfunction in vitro as evidenced by reduced transendothelial electrical resistance (TEER), altered localization and loss of endothelial junction molecules and enhanced macromolecular permeability. Inflamed BECs showed impaired Notch signaling as indicated by reduced level of the downstream targets HES-1 and HES-5. Notably, barrier function was further reduced when the Notch signaling was inhibited under inflammatory conditions, suggesting an additive effect of the Notch signaling and inflammation in BECs. In contrast, inducible overexpression of Notch-intracellular domain 1 (NICD1) rescued the detrimental effect caused by inflammation. Furthermore, we provide evidence that inflammation reduced the expression of the glycosyltransferase Lunatic Fringe (LFNG), a known positive regulator of Notch glycosylation and signaling, thereby leading to disrupted barrier function of BECs. Together, our data demonstrate the functional importance of the conserved Notch signaling pathway in control of the brain endothelial barrier and shed light on the role of LFNG in the regulation of Notch glycosylation and signaling in the adult brain vasculature in both health and disease.

Additional Metadata
Keywords Glycosylation, Inflammation, Notch signaling, Vasculature
Persistent URL dx.doi.org/10.1016/j.bbi.2017.12.016, hdl.handle.net/1765/103915
Journal Brain, Behavior, and Immunity
Citation
Derada Troletti, C. (Claudio), Lopes Pinheiro, M.A, Charabati, M. (Marc), Gowing, E. (Elizabeth), Van Het Hof, B, van der Pol, S.M.A, … de Vries, H.E. (Helga E.). (2018). Notch signaling is impaired during inflammation in a Lunatic Fringe-dependent manner. Brain, Behavior, and Immunity. doi:10.1016/j.bbi.2017.12.016