Isolating vessels from the mouse brain for gene expression analysis using laser capture microdissection

被引:52
作者
Ball, HJ [1 ]
McParland, B [1 ]
Driussi, C [1 ]
Hunt, NH [1 ]
机构
[1] Univ Sydney, Dept Pathol, Camperdown, NSW 2006, Australia
来源
BRAIN RESEARCH PROTOCOLS | 2002年 / 9卷 / 03期
基金
英国医学研究理事会;
关键词
laser capture microdissection; microvessel; cerebral malaria;
D O I
10.1016/S1385-299X(02)00147-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Studies of gene expression often examine a pool of RNA extracted from the diverse cell types making up a tissue. We have developed a method for isolating vessels from the brain in order to understand the changes occurring in the vessels during the pathogenesis of cerebral malaria. Vessels were visualised by incubating sections of mouse brain with a substrate for alkaline phosphatase. Vessels were collected by laser capture microdissection and the specificity was monitored by measuring the expression of cell-specific markers. RNA from the captured vessels was highly enriched in mRNA for genes associated with endothelial cells and pericytes. Measurement of indoleamine 2,3-dioxygenase mRNA indicated it was possible to detect changes in gene expression, due to malaria infection, occurring specifically within the vessels. Laser capture microdissection can be used to study changes in gene expression occurring at the blood-brain barrier. Crown copyright (C) 2002 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:206 / 213
页数:8
相关论文
共 11 条
[1]  
BURSTONE MS, 1960, J NATL CANCER I, V24, P1199
[2]   A high-resolution, fluorescence-based method for localization of endogenous alkaline phosphatase activity [J].
Cox, WG ;
Singer, VL .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1999, 47 (11) :1443-1455
[3]   ANALYSIS OF GENE-EXPRESSION IN SINGLE LIVE NEURONS [J].
EBERWINE, J ;
YEH, H ;
MIYASHIRO, K ;
CAO, YX ;
NAIR, S ;
FINNELL, R ;
ZETTEL, M ;
COLEMAN, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) :3010-3014
[4]   Laser capture microdissection [J].
EmmertBuck, MR ;
Bonner, RF ;
Smith, PD ;
Chuaqui, RF ;
Zhuang, ZP ;
Goldstein, SR ;
Weiss, RA ;
Liotta, LA .
SCIENCE, 1996, 274 (5289) :998-1001
[5]   Role of ICAM-1 (CD54) in the development of murine cerebral malaria [J].
Favre, N ;
Da Laperousaz, C ;
Ryffel, B ;
Weiss, NA ;
Imhof, BA ;
Rudin, W ;
Lucas, R ;
Piguet, PF .
MICROBES AND INFECTION, 1999, 1 (12) :961-968
[6]  
Gomoki G, 1939, P SOC EXP BIOL MED, V42, P23
[7]  
HANSEN AM, UNPUB INCREASED EXPR
[8]   A CYTOCHEMICAL STUDY OF CEREBROVASCULAR LESIONS IN MICE INFECTED WITH PLASMODIUM-BERGHEI [J].
POLDER, TW ;
ELING, WMC ;
JERUSALEM, CR ;
WIJERSROUW, M .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1991, 101 (01) :24-34
[9]   BREAKDOWN OF THE BLOOD-BRAIN BARRIER IN MURINE CEREBRAL MALARIA [J].
THUMWOOD, CM ;
HUNT, NH ;
CLARK, IA ;
COWDEN, WB .
PARASITOLOGY, 1988, 96 :579-589
[10]   Cerebral malaria [J].
Turner, G .
BRAIN PATHOLOGY, 1997, 7 (01) :569-582