| Literature DB >> 25411471 |
Viorica Braniste1, Maha Al-Asmakh2, Czeslawa Kowal3, Farhana Anuar2, Afrouz Abbaspour2, Miklós Tóth4, Agata Korecka2, Nadja Bakocevic5, Lai Guan Ng, Ng Lai Guan5, Parag Kundu6, Balázs Gulyás7, Christer Halldin7, Kjell Hultenby8, Harriet Nilsson9, Hans Hebert9, Bruce T Volpe10, Betty Diamond3, Sven Pettersson11.
Abstract
Pivotal to brain development and function is an intact blood-brain barrier (BBB), which acts as a gatekeeper to control the passage and exchange of molecules and nutrients between the circulatory system and the brain parenchyma. The BBB also ensures homeostasis of the central nervous system (CNS). We report that germ-free mice, beginning with intrauterine life, displayed increased BBB permeability compared to pathogen-free mice with a normal gut flora. The increased BBB permeability was maintained in germ-free mice after birth and during adulthood and was associated with reduced expression of the tight junction proteins occludin and claudin-5, which are known to regulate barrier function in endothelial tissues. Exposure of germ-free adult mice to a pathogen-free gut microbiota decreased BBB permeability and up-regulated the expression of tight junction proteins. Our results suggest that gut microbiota-BBB communication is initiated during gestation and propagated throughout life.Entities:
Mesh:
Year: 2014 PMID: 25411471 PMCID: PMC4396848 DOI: 10.1126/scitranslmed.3009759
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956