Kinetic profile of the transcriptome changes induced in the choroid plexus by peripheral inflammation

被引:100
作者
Marques, Fernanda [1 ]
Sousa, Joao C. [1 ]
Coppola, Giovanni [2 ]
Falcao, Ana M. [1 ]
Rodrigues, Ana Joao [1 ]
Geschwind, Daniel H. [2 ]
Sousa, Nuno [1 ]
Correia-Neves, Margarida [1 ]
Palha, Joana A. [1 ]
机构
[1] Univ Minho, Sch Hlth Sci, Life & Hlth Sci Res Inst ICVS, P-4710057 Braga, Portugal
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
关键词
choroid plexus; cerebrospinal fluid; lipopolysaccharide; blood-brain barrier; inflammation; transcriptome; CELL-WALL COMPONENTS; ACUTE-PHASE PROTEINS; TOLL-LIKE RECEPTOR-4; RAT-BRAIN; PROINFLAMMATORY CYTOKINES; MULTIPLE-SCLEROSIS; MESSENGER-RNAS; ENDOTOXEMIA; INVOLVEMENT; EXPRESSION;
D O I
10.1038/jcbfm.2009.15
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The choroid plexus, being part of the blood-brain barriers and responsible for the production of cerebrospinal fluid, is ideally positioned to transmit signals into and out of the brain. This study, using microarray analysis, shows that the mouse choroid plexus displays an acute-phase response after an inflammatory stimulus induced in the periphery by lipopolysaccharide (LPS). Remarkably, the response is specific to a restricted number of genes (out of a total of 24,000 genes analyzed, 252 are up-regulated and 173 are down-regulated) and transient, as it returns to basal conditions within 72 h. The up-regulated genes cluster into families implicated in immune-mediated cascades and in extracellular matrix remodeling, whereas those down-regulated participate in maintenance of the barrier function. Importantly, several acute-phase proteins, whose blood concentrations rise in response to inflammation, may contribute to the effects observed in vivo after LPS injection, as suggested by the differential response of primary choroid plexus epithelial cell cultures to LPS alone or to serum collected from animals exposed to LPS. By modulating the composition of the cerebrospinal fluid, which will ultimately influence the brain parenchyma, the choroid plexus response to inflammation may be of relevance in brain homeostasis in health and disease. Journal of Cerebral Blood Flow & Metabolism (2009) 29, 921-932; doi:10.1038/jcbfm.2009.15; published online 25 February 2009
引用
收藏
页码:921 / 932
页数:12
相关论文
共 41 条
[1]   CSF biomarkers for mild cognitive impairment and early Alzheimer's disease [J].
Andreasen, N ;
Blennow, K .
CLINICAL NEUROLOGY AND NEUROSURGERY, 2005, 107 (03) :165-173
[2]   Time course and distribution of inflammatory and neurodegenerative events suggest structural bases for the pathogenesis of experimental autoimmune encephalomyelitis [J].
Brown, David A. ;
Sawchenko, Paul E. .
JOURNAL OF COMPARATIVE NEUROLOGY, 2007, 502 (02) :236-260
[3]   The systemic reaction during inflammation: The acute-phase proteins [J].
Ceciliani, F ;
Giordano, A ;
Spagnolo, V .
PROTEIN AND PEPTIDE LETTERS, 2002, 9 (03) :211-223
[4]   Toll-like receptor 4 on nonhematopoietic cells sustains CNS inflammation during endotoxemia, independent of systemic cytokines [J].
Chakravarty, S ;
Herkenham, M .
JOURNAL OF NEUROSCIENCE, 2005, 25 (07) :1788-1796
[5]   Cutting edge: TLR2 is a functional receptor for acute-phase serum amyloid A [J].
Cheng, Ni ;
He, Rong ;
Tian, Jun ;
Ye, Patrick P. ;
Ye, Richard D. .
JOURNAL OF IMMUNOLOGY, 2008, 181 (01) :22-26
[6]  
Chodobski A, 2001, MICROSC RES TECHNIQ, V52, P65
[7]   TLR pathways and IFN-regulatory factors: To each its own [J].
Colonna, Marco .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2007, 37 (02) :306-309
[8]   Streptococcus suis serotype 2, an important swine and human pathogen, induces strong systemic and cerebral inflammatory responses in a mouse model of infection [J].
Dominguez-Punaro, Maria C. ;
Segura, Mariela ;
Plante, Marie-Michele ;
Lacouture, Sonia ;
Rivest, Serge ;
Gottschalk, Marcelo .
JOURNAL OF IMMUNOLOGY, 2007, 179 (03) :1842-1854
[9]   The choroid plexus in the rise, fall and repair of the brain [J].
Emerich, DF ;
Skinner, SJM ;
Borlongan, CV ;
Vasconcellos, AV ;
Thanos, CG .
BIOESSAYS, 2005, 27 (03) :262-274
[10]  
Engelhardt B, 2001, MICROSC RES TECHNIQ, V52, P112, DOI 10.1002/1097-0029(20010101)52:1<112::AID-JEMT13>3.0.CO