## Abstract Three genetic mouse models were examined to define effects of bone morphogenetic protein (BMP) signalling on gene expression in normal and injured adult brain. CaMKII‐Cre eliminated the BMP receptor Acvr1 (Alk2) and the common TGFβ superfamily signal mediator Smad4 or activated a consti
Altered expression of randomly selected genes in mouse hippocampus after traumatic brain injury
✍ Scribed by Yan Long; Linglong Zou; Hao Liu; Holly Lu; Xiaoqing Yuan; Claudia S. Robertson; Keyi Yang
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 335 KB
- Volume
- 71
- Category
- Article
- ISSN
- 0360-4012
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Using a cDNA microarray method, we analyzed gene expression profiles in mouse hippocampus after traumatic brain injury (TBI). Of 6,400 randomly selected arrayed genes and expressed sequence tags from a mouse cDNA library, 253 were found to be differentially expressed (106 increased and 147 decreased). Genes involved in cell homeostasis and calcium signaling were primarily up‐regulated while those encoding mitochondrial enzymes, metabolic molecules, and structural proteins were predominantly down‐regulated. Equal numbers of genes related to inflammatory reactions showed increased or decreased expression. Importantly, a large proportion of the dysregulated genes we identified have not been reported as differentially expressed in TBI models. Semiquantitative reverse‐transcriptase polymerase chain reaction (RT‐PCR) analyses of representative genes confirmed the validity of the corresponding microarray findings. Thus, our microarray‐based evaluation of gene expression in traumatically injured hippocampus identified both known and novel genes that respond to TBI. Further investigation of these candidate molecules may suggest new ways to attenuate the traumatic effects of brain injury. © 2002 Wiley‐Liss, Inc.
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