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| Research article summary (published 30 Aug 2009): |
Identification and function of agrin expressed in rat brain microvessels.
Full Abstract
Agrin isoforms in the brain microvessels were investigated. Brain microvessels prepared from rat cerebral cortex expressed the short amino terminal (SN) isoform, which contains a transmembrane sequence of SN agrin, and the long amino terminal (LN) isoform, which contains a signal sequence for secretion of LN agrin, were detected in the microvessels. The expression of LN form mRNA in comparison with that of SN form was higher in the brain microvessels than in the cerebral cortex, indicating preferential expression of LN form agrin in the microvessels. In addition, the amino-terminal sequence of agrin expressed in the rat brain microvessels was determined by rapid amplification of 5' cDNA end (5'-RACE). The sequence contained a cluster of hydrophobic amino acids, which may form a signal sequence for secretion. Transfection of expression vector coding amino-terminal sequence of LN agrin fused with green fluorescence protein (GFP) into human embryonic kidney (HEK293) cells caused expression of the protein in the cell as well as in the medium, whereas SN agrin fused with GFP expressed at the cell surface. These results show that the major form of agrin expressed in the brain microvessels is of basal lamina-associated LN agrin and suggest that LN agrin may play a role in molecular organization at the interface between the parenchyma cells and microvessels.
Author information
Author/s: Kobayashi, Hideyuki (H);
Affiliation: Department of Chemistry, School of Medicine, University of Occupational and Environmental Health, Japan, Yahatanishi-ku, Kitakyushu 807-8555, Japan.
Journal and publication information
Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
Journal: Journal of UOEH (J UOEH), published in Japan. (Language: eng)
Reference: 2009-Sep; vol 31 (issue 3) : pp 219-30
Dates: Created 2009/09/15; Completed 2009/11/02;
PMID: 19750929, status: MEDLINE (last retrieval date: 11/2/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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