TY - JOUR
T1 - Brain response to traumatic brain injury in wild-type and interleukin-6 knockout mice: a microarray analysis
AU - Poulsen, Christian Bjørn
AU - Penkowa, Milena
AU - Borup, Rehannah
AU - Nielsen, Finn Cilius
AU - Cáceres, Mario
AU - Quintana, Albert
AU - Molinero, Amalia
AU - Carrasco, Javier
AU - Giralt, Mercedes
AU - Hidalgo, Juan
N1 - Keywords: Analysis of Variance; Animals; Brain; Brain Injuries; Cluster Analysis; Disease Progression; Down-Regulation; Gene Expression Profiling; Interleukin-6; Mice; Mice, Inbred C57BL; Mice, Knockout; Oligonucleotide Array Sequence Analysis; Up-Regulation
PY - 2005
Y1 - 2005
N2 - Traumatic injury to the brain is one of the leading causes of injury-related death or disability. Brain response to injury is orchestrated by cytokines, such as interleukin (IL)-6, but the full repertoire of responses involved is not well known. We here report the results obtained with microarrays in wild-type and IL-6 knockout mice subjected to a cryolesion of the somatosensorial cortex and killed at 0, 1, 4, 8 and 16 days post-lesion. Overall gene expression was analyzed by using Affymetrix genechips/oligonucleotide arrays with approximately 12,400 probe sets corresponding to approximately 10,000 different murine genes (MG_U74Av2). A robust, conventional statistical method (two-way anova) was employed to select the genes significantly affected. An orderly pattern of gene responses was clearly detected, with genes being up- or down-regulated at specific timings consistent with the processes involved in the initial tissue injury and later regeneration of the parenchyma. IL-6 deficiency showed a dramatic effect in the expression of many genes, especially in the 1 day post-lesion timing, which presumably underlies the poor capacity of IL-6 knockout mice to cope with brain damage. The results highlight the importance of IL-6 controlling the response of the brain to injury as well as the suitability of microarrays for identifying specific targets worthy of further study.
AB - Traumatic injury to the brain is one of the leading causes of injury-related death or disability. Brain response to injury is orchestrated by cytokines, such as interleukin (IL)-6, but the full repertoire of responses involved is not well known. We here report the results obtained with microarrays in wild-type and IL-6 knockout mice subjected to a cryolesion of the somatosensorial cortex and killed at 0, 1, 4, 8 and 16 days post-lesion. Overall gene expression was analyzed by using Affymetrix genechips/oligonucleotide arrays with approximately 12,400 probe sets corresponding to approximately 10,000 different murine genes (MG_U74Av2). A robust, conventional statistical method (two-way anova) was employed to select the genes significantly affected. An orderly pattern of gene responses was clearly detected, with genes being up- or down-regulated at specific timings consistent with the processes involved in the initial tissue injury and later regeneration of the parenchyma. IL-6 deficiency showed a dramatic effect in the expression of many genes, especially in the 1 day post-lesion timing, which presumably underlies the poor capacity of IL-6 knockout mice to cope with brain damage. The results highlight the importance of IL-6 controlling the response of the brain to injury as well as the suitability of microarrays for identifying specific targets worthy of further study.
U2 - 10.1111/j.1471-4159.2004.02877.x
DO - 10.1111/j.1471-4159.2004.02877.x
M3 - Journal article
C2 - 15663489
SN - 0022-3042
VL - 92
SP - 417
EP - 432
JO - Journal of Neurochemistry
JF - Journal of Neurochemistry
IS - 2
ER -