4.3 Article

Serotype b of Aggregatibacter actinomycetemcomitans triggers pro-inflammatory responses and amyloid beta secretion in hippocampal cells: a novel link between periodontitis and Alzheimer′s disease?

期刊

JOURNAL OF ORAL MICROBIOLOGY
卷 11, 期 1, 页码 -

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/20002297.2019.1586423

关键词

Periodontitis; Alzheimer ' s disease; inflammation; cytokines; microglia; neurons

资金

  1. National Commission for Scientific and Technological Research [FONDECYT 1150736, FONDECYT 1181780]
  2. Faculty of Dentistry grant [FIOUCh 2017-006]
  3. Regional Development Program of the International Association for Dental Research (RDP-IADR)
  4. BNI [P-09-015]

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Introduction: Previous reports have proposed that Periodontal disease (PDis) predisposes to Alzheimer's disease (AD), both highly prevalent pathologies among the elderly. The bacteria Aggregatibacter actinomycetemcomitans (Aa), associated with the most aggressive forms of PDis, are classified in different serotypes with distinct virulence according to the antigenicity of their lipopolysaccharide (LPS). Methods: Here, we determined the effects of purified LPS, from serotypes a, b or c of Aa, on primary cultures of microglia or mixed hippocampal cells. Results: We found that both culture types exhibited higher levels of inflammatory cytokines (IL-1 beta, IL-6 and TNF alpha) when treated with serotype b-LPS, compared with controls, as quantified by qPCR and/or ELISA. Also, cultures treated with serotype a-LPS displayed increased mRNA levels of the modulatory cytokines IL-4 and IL-10. Mixed hippocampal cultures treated with serotype b-LPS exhibited severe neuronal morphological changes and displayed increased levels of secreted A beta(1-42) peptide. These results indicate that LPS from different Aa serotypes triggers discriminatory immune responses, which differentially affect primary hippocampal cells. Conclusion: Altogether, our results show that treatment with serotype b-LPS triggers the secretion of proinflammatory cytokines by microglia, induces neurite shrinking, and increases the extracellular A beta 1-42 levels, all features strongly associated with the etiology of AD.

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