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Induction of novel cytokines and chemokines by advanced glycation endproducts determined with a cytometric bead array

Citation

Berbaurn, K and Shanmugam, K and Stuchbury, G and Wiede, F and Korner, H and Munch, G, Induction of novel cytokines and chemokines by advanced glycation endproducts determined with a cytometric bead array, Cytokine, 41, (3) pp. 198-203. ISSN 1043-4666 (2008) [Refereed Article]

DOI: doi:10.1016/j.cyto.2007.11.012

Abstract

Advanced glycation endproducts (AGEs) accumulate on long-lived protein deposits, e.g. those composed of β 2-microglobulin (in dialysis-related amyloidosis) or β-amyloid peptide (in Alzheimer's disease). When AGEs bind to the "receptor for advanced glycation endproducts", they activate redox-sensitive transcription factors such as NF-κB, and subsequently induce the expression of pro-inflammatory cytokines such as IL-1, IL-6 and TNF-α. Using a cytokine bead array, we have further analyzed the Bovine Serum Albumin (BSA)-AGE induced expression of selected cytokines/chemokines in two murine cell lines, RAW 264.7 macrophages and N-11 microglia. Our study showed that monocyte chemoattractant protein-1 (MCP-1) and tumor necrosis factor (TNF-α) were both released in a time-dependent manner from both RAW 264.7 macrophages and N-11 microglia upon stimulation with BSA-AGE or lipopolysaccharide (LPS), which was used as a positive control. Interestingly, MCP-1 was also constitutively expressed by unstimulated cells, although at a lower levels. Much higher levels of IL-6 were secreted by RAW 264.7 macrophages than by N-11 microglia in response to both stimuli. IL-12p70, interferon-γ and the anti-inflammatory cytokine IL-10 were not induced by either LPS or BSA-AGE. Our results indicate a very similar pattern of chemokine and cytokine expression induced by such different ligands as AGEs and LPS indicating similar or convergent downstream signaling pathways. © 2007 Elsevier Ltd. All rights reserved.

Item Details

Item Type:Refereed Article
Research Division:Medical and Health Sciences
Research Group:Neurosciences
Research Field:Central Nervous System
Objective Division:Health
Objective Group:Clinical Health (Organs, Diseases and Abnormal Conditions)
Objective Field:Infectious Diseases
Author:Korner, H (Professor Heinrich Korner)
ID Code:72539
Year Published:2008
Web of Science® Times Cited:33
Deposited By:Research Division
Deposited On:2011-08-29
Last Modified:2011-08-29
Downloads:0

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