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NeuroMolecular Medicine

, Volume 20, Issue 4, pp 504–514 | Cite as

Metabolism of Docosahexaenoic Acid (DHA) Induces Pyroptosis in BV-2 Microglial Cells

  • Malavika Srikanth
  • Kalashobini Chandrasaharan
  • Xinyuan Zhao
  • Kanokporn Chayaburakul
  • Wei-Yi Ong
  • Deron R. HerrEmail author
Original Paper

Abstract

DHA is one of the most abundant fatty acids in the brain, largely present in stores of membrane phospholipids. It is readily released by the action of phospholipase A2 and is known to induce anti-inflammatory and neurotrophic effects. It is not thought to contribute to proinflammatory processes in the brain. In this study, an immortalized murine microglia cell line (BV-2) was used to evaluate the effect of DHA on neuroinflammatory cells. Pretreatment of BV-2 cells with low concentrations of DHA (30 µM) attenuates lipopolysaccharide-mediated inflammatory cytokine gene expression, consistent with known anti-inflammatory effects. However, higher (but still physiologically relevant) concentrations of DHA (200 µM) induce profound cell swelling and a reduction of viability. This is accompanied by increases in the expressions of inflammatory cytokine and lipoxygenase genes, activation of caspase-1 activity, and release of IL1β, indicating that cells were undergoing a proinflammatory cell death program known as pyroptosis. This process could be attenuated by pharmacological inhibition of 12-lipoxygenase (12-LOX, Alox12e), but not by inhibition of 5-LOX or 15-LOX. Cumulatively, these data demonstrate that DHA has an anti-inflammatory effect on microglial cells, but its metabolism by 12-LOX generates one or more products that activate a proinflammatory cell death program.

Keywords

Neuroinflammation Proptosis Microglia Docosahexaenoic acid (DHA) Lipoxygenase 12-LOX 

Abbreviations

AA

Arachidonic acid

CNS

Central nervous system

DAMP

Damage-associated molecular pattern

DHA

Docosahexaenoic acid

DMEM

Dulbecco’s modified Eagle’s medium

ETI

Eicosatrienoic acid

LPS

Lipopolysaccharide

MTT

3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide

PRR

Pattern recognition receptor

PUFA

Polyunsaturated fatty acid

SPM

Specialized pro-resolving mediators

Notes

Acknowledgements

The authors are grateful to Low Kay En and the Electron Microscopy Unit at the National University of Singapore for expert technical assistance with the scanning electron microscopy, and to Pabba Anubharath for expert technical assistance with the processing of time-lapse microscopy data. This work was supported by the Ministry of Education, Singapore (T1-2016 Sep-11, D.R.H.); the National Medical Research Council, Singapore (NMRC/CIRG/1410/2014, W.Y.O.); and the National University Health System (NUHSRO/2014/085/AF-Partner/01, D.R.H.).

Compliance with Ethical Standards

Conflict of interest

The authors declare no conflict of interest. The founding sponsors had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, and in the decision to publish the results.

Supplementary material

Supplementary data 1 Time-lapse video microscopy of BV-2 cells treated with vehicle. Total video length: 4 hours. (MP4 31248 KB)

Supplementary data 2 Time-lapse video microscopy of BV-2 cells treated with 200 μM DHA. Total video length: 4 hours. (MP4 31238 KB)

Supplementary data 3 Time-lapse video microscopy of BV-2 cells treated with 200 μM cisplatin (CDDP). Total video length: 4 hours. (MP4 31222 KB)

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Department of Pharmacology, Yong Loo Lin School of Medicine, National University Health SystemNational University of SingaporeSingaporeSingapore
  2. 2.Anatomy Unit, Faculty of ScienceRangsit UniversityPatum ThaniThailand
  3. 3.Department of Anatomy, Yong Loo Lin School of Medicine, National University Health SystemNational University of SingaporeSingaporeSingapore
  4. 4.Department of BiologySan Diego State UniversitySan DiegoUSA

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