RRC ID 152
Author Ago T, Kitazono T, Kuroda J, Kumai Y, Kamouchi M, Ooboshi H, Wakisaka M, Kawahara T, Rokutan K, Ibayashi S, Iida M.
Title NAD(P)H oxidases in rat basilar arterial endothelial cells.
Journal Stroke
Abstract BACKGROUND AND PURPOSE:Reactive oxygen species (ROS) may play a critical role in the regulation of vascular tone and development of vascular diseases, such as stroke. NAD(P)H oxidase is a major source of ROS in vascular cells, including endothelial cells. It has been considered that Nox2 and Nox4 are exclusively expressed among Nox homologues in the endothelial cells of noncerebral blood vessels. However, the precise molecular identity of the NAD(P)H oxidase in the endothelial cells of the cerebral arteries is not fully understood. We examined the expression of Nox homologues and their activation mechanism in the endothelial cells of the cerebral arteries.
METHODS:We isolated and cultured basilar artery endothelial cells (BAECs) of Sprague-Dawley rats. Expression of NAD(P)H oxidase was examined by reverse-transcription-polymerase chain reaction (RT-PCR) and immunohistological staining.
RESULTS:RT-PCR disclosed abundant expression of Nox4 with marginal Nox2 in BAEC. In addition, Nox1 was expressed highly both at mRNA and protein levels in BAECs. Immunohistological staining also showed the prominent expression of Nox1 in the endothelial cells of the basilar artery. With respect to the cytosolic components of NAD(P)H oxidases, BAECs expressed p67phox and, to a lesser extent, p47phox, Noxo1, and Noxa1. Both NADH and NADPH induced superoxide production of the BAEC membranes. The phagocyte-type cytosolic components, p47phox and p67phox, significantly enhanced the NADH-induced superoxide production of the BAEC membranes, whereas the components failed to increase the NADPH-induced superoxide production.
CONCLUSIONS:Nox1 is highly expressed in the endothelial cells of the cerebral arteries along with Nox2 and Nox4, and the endothelial NAD(P)H oxidase of the cerebral arteries may have a unique activation mechanism by the phagocyte-type cytosolic components.
Volume 36(5)
Pages 1040-6
Published 2005-5
DOI 10.1161/01.STR.0000163111.05825.0b
PII 01.STR.0000163111.05825.0b
PMID 15845888
MeSH Animals Basilar Artery / cytology Basilar Artery / enzymology* Endothelial Cells / cytology Endothelial Cells / enzymology Endothelium, Vascular / cytology Endothelium, Vascular / enzymology* Male NADH, NADPH Oxidoreductases / genetics NADH, NADPH Oxidoreductases / metabolism NADPH Oxidase 1 NADPH Oxidases / metabolism* Phosphoproteins / biosynthesis Phosphoproteins / genetics RNA, Messenger / metabolism Rats Rats, Sprague-Dawley Superoxides / metabolism
IF 6.058
Times Cited 105
WOS Category CLINICAL NEUROLOGY PERIPHERAL VASCULAR DISEASE
Resource
Rats