Your browser doesn't support javascript.
loading
Defective Function of the Blood-Brain Barrier in a Stroke-Prone Spontaneously Hypertensive Rat: Evaluation in an In Vitro Cell Culture Model.
Nakagawa, Shinsuke; Ohara, Hiroki; Niwa, Masami; Yamagata, Kazuo; Nabika, Toru.
Afiliación
  • Nakagawa S; Department of Medical Pharmacology, Nagasaki University Graduate School of Biomedical Sciences, 1-12-4 Sakamoto, Nagasaki, 852-8523, Japan. shin3@fukuoka-u.ac.jp.
  • Ohara H; Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.
  • Niwa M; BBB Laboratory, PharmaCo-Cell Company, Ltd., 6-19-203 Chitose, Nagasaki, 852-8135, Japan.
  • Yamagata K; Laboratory of Molecular Health of Food, Department of Food Bioscience and Biotechnology, College of Bioresource Sciences, Nihon University (NUBS), 1866, Kameino, Fujisawa, Kanagawa, 252-8510, Japan.
  • Nabika T; Department of Functional Pathology, Shimane University Faculty of Medicine, Izumo, Japan.
Cell Mol Neurobiol ; 42(1): 243-253, 2022 Jan.
Article en En | MEDLINE | ID: mdl-32648236
ABSTRACT
The blood-brain barrier (BBB) comprises three cell types brain capillary endothelial cells (BECs), astrocytes, and pericytes. Abnormal interaction among these cells may induce BBB dysfunction and lead to cerebrovascular diseases. The stroke-prone spontaneously hypertensive rat (SHRSP) harbors a defective BBB, so we designed the present study to examine the role of these three cell types in a functional disorder of the BBB in SHRSP in order to elucidate the role of these cells in the BBB more generally. To this end, we employed a unique in vitro model of BBB, in which various combinations of the cells could be tested. The three types of cells were prepared from both SHRSPs and Wistar Kyoto rats (WKYs). They were then co-cultured in various combinations to construct in vitro BBB models. The barrier function of the models was estimated by measuring transendothelial electrical resistance and the permeability of the endothelial monolayer to sodium fluorescein. The in vitro models revealed that (1) BECs from SHRSPs had an inherent lower barrier function, (2) astrocytes of SHRSPs had an impaired ability to induce barrier function in BECs, although (3) both pericytes and astrocytes of SHRSPs and WKYs could potentiate the barrier function of BECs under co-culture conditions. Furthermore, we found that claudin-5 expression was consistently lower in models that used BECs and/or SHRSP astrocytes. These results suggested that defective interaction among BBB cells-especially BECs and astrocytes-was responsible for a functional disorder of the BBB in SHRSPs.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Barrera Hematoencefálica / Accidente Cerebrovascular Límite: Animals Idioma: En Revista: Cell Mol Neurobiol Año: 2022 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Barrera Hematoencefálica / Accidente Cerebrovascular Límite: Animals Idioma: En Revista: Cell Mol Neurobiol Año: 2022 Tipo del documento: Article País de afiliación: Japón