Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/126869
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Type: Journal article
Title: Lipopolysaccharide promotes Drp1-dependent mitochondrial fission and associated inflammatory responses in macrophages
Author: Kapetanovic, R.
Afroz, S.F.
Ramnath, D.
Lawrence, G.M.E.P.
Okada, T.
Curson, J.E.B.
de Bruin, J.
Fairlie, D.P.
Schroder, K.
St John, J.C.
Blumenthal, A.
Sweet, M.J.
Citation: Immunology and Cell Biology, 2020; 98(7):528-539
Publisher: Wiley
Issue Date: 2020
ISSN: 0818-9641
1440-1711
Statement of
Responsibility: 
Ronan Kapetanovic, Syeda Farhana Afroz, Divya Ramnath, Grace MEP Lawrence, Takashi Okada, James EB Curson, Jost de Bruin, David P Fairlie, Kate Schroder, Justin C St John, Antje Blumenthal, Matthew J Sweet
Abstract: Mitochondria have a multitude of functions, including energy generation and cell signaling. Recent evidence suggests that mitochondrial dynamics (i.e. the balance between mitochondrial fission and fusion) also regulate immune functions. Here, we reveal that lipopolysaccharide (LPS) stimulation increases mitochondrial numbers in mouse bone marrow‐derived macrophages (BMMs) and human monocyte‐derived macrophages. In BMMs, this response requires Toll‐like receptor 4 (Tlr4) and the TLR adaptor protein myeloid differentiation primary response 88 (MyD88) but is independent of mitochondrial biogenesis. Consistent with this phenomenon being a consequence of mitochondrial fission, the dynamin‐related protein 1 (Drp1) GTPase that promotes mitochondrial fission is enriched on mitochondria in LPS‐activated macrophages and is required for the LPS‐mediated increase in mitochondrial numbers in both BMMs and mouse embryonic fibroblasts. Pharmacological agents that skew toward mitochondrial fusion also abrogated this response. LPS triggered acute Drp1 phosphorylation at serine 635 (S635), followed by sustained Drp1 dephosphorylation at serine 656 (S656), in BMMs. LPS‐induced S656 dephosphorylation was abrogated in MyD88‐deficient BMMs, suggesting that this post‐translational modification is particularly important for Tlr4‐inducible fission. Pharmacological or genetic targeting of Tlr4‐inducible fission had selective effects on inflammatory mediator production, with LPS‐inducible mitochondrial fission promoting the expression and/or secretion of a subset of inflammatory mediators in BMMs and mouse embryonic fibroblasts. Thus, triggering of Tlr4 results in MyD88‐dependent activation of Drp1, leading to inducible mitochondrial fission and subsequent inflammatory responses in macrophages.
Keywords: Dynamin-related protein 1; lipopolysaccharide; macrophage; mitochondrial dynamics; mitochondrial fission; Toll-like receptor
Rights: © 2020 The Authors. Immunology & Cell Biology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
DOI: 10.1111/imcb.12363
Grant ID: http://purl.org/au-research/grants/nhmrc/1125316
http://purl.org/au-research/grants/nhmrc/1160106
http://purl.org/au-research/grants/nhmrc/1107914
http://purl.org/au-research/grants/nhmrc/1117017
http://purl.org/au-research/grants/arc/CE140100011
http://purl.org/au-research/grants/arc/DE130100470
http://purl.org/au-research/grants/nhmrc/1141131
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