Aging enhances classical activation but mitigates alternative activation in the central nervous system.

Aging enhances classical activation but mitigates alternative activation in the central nervous system.
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DOI:
10.1016/j.neurobiolaging.2012.12.014
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发表时间:
2013-06
影响因子:
4.2
通讯作者:
Morgan D
Morgan D
中科院分区:
医学2区
文献类型:
--
作者:
Lee DC;Ruiz CR;Lebson L;Selenica ML;Rizer J;Hunt JB Jr;Rojiani R;Reid P;Kammath S;Nash K;Dickey CA;Gordon M;Morgan D

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The role of microglia/ macrophages during neuroinflammation and neurodegenerative diseases remains controversial. To date, at least two activations states have been suggested consisting of a classical response (M1) and the alternative response (M2). Identifying selective biomarkers of microglia that representative their functional activation states may help elucidate disease course and understand repair mechanisms. Two cocktails containing either TNF-α, IL-12, and IL-1β (referred to as CKT-1) or IL-13 and IL-4 (referred to CKT-2) were injections into the hippocampus of mice aged 6, 12, or 24 months. Microarray analysis was performed on hippocampal tissue 3 days post injection. Gene transcripts were compared between CKT-1 versus CKT-2 stimulator cocktails. Several selective transcripts expressed for the CKT-1 included CXCL13, haptoglobin, MARCO, and calgranulin B, while a smaller subset of genes was selectively induced by the CKT-2 and consisted of FIZZ1, IGF-1, and EAR 11. Importantly, selective transcripts were induced at all ages by CKT-1, whereas selective gene transcripts induced by CKT-2 decreased with age suggesting an age-related reduction in the IL-4/ IL-13 signaling pathway.
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