Journal
EXPERIMENTAL NEUROLOGY
Volume 182, Issue 1, Pages 135-141Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/S0014-4886(03)00057-8
Keywords
glial activation; neuroinflammation; nitric oxide; microglia; astrocyte; neurodegeneration; IL-1; IL-6; TNF-alpha
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Funding
- NIA NIH HHS [AG13499] Funding Source: Medline
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Glial activation during aging was analyzed in primary glia cultured from brain regions sampled across the life span. An initial study showed that phenotypes of activated astrocytes and microglia from aging rat cerebral cortex persisted in primary cultures (Neurobiol. Aging 19 (1998), 97). We extend these findings by examining effects of age on the activation of glial cultures from adult rat brain in response to lipopolysaccharide (LPS), an inflammatory stimulus. Mixed glia from F344 male rats, aged 3 and 24 months, cultured from cerebral cortex (Cx), hippocampus (He), and striatum (St), were assayed for cytokines implicated in Alzheimer's disease: IL-1alpha, IL-1beta, IL-6, and TNF-alpha. Regional differences across all age groups included consistently lower expression of these cytokines in glia derived from Cx than He and St. Aging increased basal IL-6 mRNA and secretion by greater than or equal to3-fold in glia from Cx and He. Aging also increased LPS-induced IL-1 and IL-6 in He more than in Cx, whereas no significant effects of age were seen in St-derived glial cytokines. TNF-alpha secretion did not differ by donor age (basal or LPS-induced). Nitric oxide production by microglia from Cx of aging brains showed a smaller induction in response to LPS, with proportionately less neurotoxicity. Thus, glial activation during aging shows regional selectivity in cytokine expression, with opposite effects of aging on the increased inducibility of IL-1 and IL-6 vs the decreased production of nitric oxide. (C) 2003 Elsevier Science (USA). All rights reserved.
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