Delta like 4 regulates cerebrovascular development and endothelial integrity via DLL4-NOTCH-CLDN5 pathway and is vulnerable to neonatal hyperoxia.

Autor: Ke X; Department of Pediatrics Division of Neonatology, Children's Mercy, Kansas City, MO, USA., Xia S; Department of Pediatrics Division of Neonatology, Children's Mercy, Kansas City, MO, USA., Yu W; Department of Pediatrics Division of Neonatology, Children's Mercy, Kansas City, MO, USA., Mabry S; Department of Pediatrics Division of Neonatology, Children's Mercy, Kansas City, MO, USA., Fu Q; Department of Pediatrics Division of Neonatology, Children's Mercy, Kansas City, MO, USA., Menden HL; Department of Pediatrics Division of Neonatology, Children's Mercy, Kansas City, MO, USA., Sampath V; Department of Pediatrics Division of Neonatology, Children's Mercy, Kansas City, MO, USA., Lane RH; Department of Administration, Children Mercy Research Institute, Children's Mercy, Kansas City, MO, USA.
Jazyk: angličtina
Zdroj: The Journal of physiology [J Physiol] 2024 May; Vol. 602 (10), pp. 2265-2285. Date of Electronic Publication: 2024 Apr 17.
DOI: 10.1113/JP285716
Abstrakt: The mechanisms governing brain vascularization during development remain poorly understood. A key regulator of developmental vascularization is delta like 4 (DLL4), a Notch ligand prominently expressed in endothelial cells (EC). Exposure to hyperoxia in premature infants can disrupt the development and functions of cerebral blood vessels and lead to long-term cognitive impairment. However, its role in cerebral vascular development and the impact of postnatal hyperoxia on DLL4 expression in mouse brain EC have not been explored. We determined the DLL4 expression pattern and its downstream signalling gene expression in brain EC using Dll4 +/+ and Dll4 +/LacZ mice. We also performed in vitro studies using human brain microvascular endothelial cells. Finally, we determined Dll4 and Cldn5 expression in mouse brain EC exposed to postnatal hyperoxia. DLL4 is expressed in various cell types, with EC being the predominant one in immature brains. Moreover, DLL4 deficiency leads to persistent abnormalities in brain microvasculature and increased vascular permeability both in vivo and in vitro. We have identified that DLL4 insufficiency compromises endothelial integrity through the NOTCH-NICD-RBPJ-CLDN5 pathway, resulting in the downregulation of the tight junction protein claudin 5 (CLDN5). Finally, exposure to neonatal hyperoxia reduces DLL4 and CLDN5 expression in developing mouse brain EC. We reveal that DLL4 is indispensable for brain vascular development and maintaining the blood-brain barrier's function and is repressed by neonatal hyperoxia. We speculate that reduced DLL4 signalling in brain EC may contribute to the impaired brain development observed in neonates exposed to hyperoxia. KEY POINTS: The role of delta like 4 (DLL4), a Notch ligand in vascular endothelial cells, in brain vascular development and functions remains unknown. We demonstrate that DLL4 is expressed at a high level during postnatal brain development in immature brains and DLL4 insufficiency leads to abnormal cerebral vasculature and increases vascular permeability both in vivo and in vitro. We identify that DLL4  regulates endothelial integrity through NOTCH-NICD-RBPJ-CLDN5 signalling. Dll4 and Cldn5 expression are decreased in mouse brain endothelial cells exposed to postnatal hyperoxia.
(© 2024 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society.)
Databáze: MEDLINE
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