Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway

Natural killer (NK) cells provide the first line of defense against malaria parasite infection. However, the molecular mechanisms through which NK cells are activated by parasites are largely unknown, so is the molecular basis underlying the variation in NK cell responses to malaria infection in the...

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Main Authors: Ye, Weijian, Chew, Marvin, Hou, Jue, Lai, Fritz, Leopold, Stije J., Loo, Hooi Linn, Ghose, Aniruddha, Dutta, Ashok K., Chen, Qingfeng, Ooi, Eng Eong, White, Nicholas J., Dondorp, Arjen M., Preiser, Peter, Chen, Jianzhu
Other Authors: Goodier, Martin
Format: Article
Language:English
Published: 2019
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Online Access:https://hdl.handle.net/10356/106329
http://hdl.handle.net/10220/47420
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1063292023-02-28T17:07:10Z Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway Ye, Weijian Chew, Marvin Hou, Jue Lai, Fritz Leopold, Stije J. Loo, Hooi Linn Ghose, Aniruddha Dutta, Ashok K. Chen, Qingfeng Ooi, Eng Eong White, Nicholas J. Dondorp, Arjen M. Preiser, Peter Chen, Jianzhu Goodier, Martin School of Biological Sciences Singapore-MIT Alliance Programme NK Cells Malaria DRNTU::Science::Biological sciences Natural killer (NK) cells provide the first line of defense against malaria parasite infection. However, the molecular mechanisms through which NK cells are activated by parasites are largely unknown, so is the molecular basis underlying the variation in NK cell responses to malaria infection in the human population. Here, we compared transcriptional profiles of responding and non-responding NK cells following exposure to Plasmodium-infected red blood cells (iRBCs) and identified MDA5, a RIG-I-like receptor involved in sensing cytosolic RNAs, to be differentially expressed. Knockout of MDA5 in responding human NK cells by CRISPR/cas9 abolished NK cell activation, IFN-γ secretion, lysis of iRBCs. Similarly, inhibition of TBK1/IKKε, an effector molecule downstream of MDA5, also inhibited activation of responding NK cells. Conversely, activation of MDA5 by liposome-packaged poly I:C restored non-responding NK cells to lyse iRBCs. We further show that microvesicles containing large parasite RNAs from iRBCs activated NK cells by fusing with NK cells. These findings suggest that NK cells are activated through the MDA5 pathway by parasite RNAs that are delivered to the cytoplasm of NK cells by microvesicles from iRBCs. The difference in MDA5 expression between responding and non-responding NK cells following exposure to iRBCs likely contributes to the variation in NK cell responses to malaria infection in the human population. NRF (Natl Research Foundation, S’pore) Published version 2019-01-08T04:56:35Z 2019-12-06T22:09:16Z 2019-01-08T04:56:35Z 2019-12-06T22:09:16Z 2018 Journal Article Ye, W., Chew, M., Hou, J., Lai, F., Leopold, S. J., Loo, H. L., . . . Chen, J. (2018). Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway. PLOS Pathogens, 14(10), e1007298-. doi:10.1371/journal.ppat.1007298 1553-7366 https://hdl.handle.net/10356/106329 http://hdl.handle.net/10220/47420 10.1371/journal.ppat.1007298 en PLOS Pathogens © 2018 Ye et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 21 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic NK Cells
Malaria
DRNTU::Science::Biological sciences
spellingShingle NK Cells
Malaria
DRNTU::Science::Biological sciences
Ye, Weijian
Chew, Marvin
Hou, Jue
Lai, Fritz
Leopold, Stije J.
Loo, Hooi Linn
Ghose, Aniruddha
Dutta, Ashok K.
Chen, Qingfeng
Ooi, Eng Eong
White, Nicholas J.
Dondorp, Arjen M.
Preiser, Peter
Chen, Jianzhu
Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway
description Natural killer (NK) cells provide the first line of defense against malaria parasite infection. However, the molecular mechanisms through which NK cells are activated by parasites are largely unknown, so is the molecular basis underlying the variation in NK cell responses to malaria infection in the human population. Here, we compared transcriptional profiles of responding and non-responding NK cells following exposure to Plasmodium-infected red blood cells (iRBCs) and identified MDA5, a RIG-I-like receptor involved in sensing cytosolic RNAs, to be differentially expressed. Knockout of MDA5 in responding human NK cells by CRISPR/cas9 abolished NK cell activation, IFN-γ secretion, lysis of iRBCs. Similarly, inhibition of TBK1/IKKε, an effector molecule downstream of MDA5, also inhibited activation of responding NK cells. Conversely, activation of MDA5 by liposome-packaged poly I:C restored non-responding NK cells to lyse iRBCs. We further show that microvesicles containing large parasite RNAs from iRBCs activated NK cells by fusing with NK cells. These findings suggest that NK cells are activated through the MDA5 pathway by parasite RNAs that are delivered to the cytoplasm of NK cells by microvesicles from iRBCs. The difference in MDA5 expression between responding and non-responding NK cells following exposure to iRBCs likely contributes to the variation in NK cell responses to malaria infection in the human population.
author2 Goodier, Martin
author_facet Goodier, Martin
Ye, Weijian
Chew, Marvin
Hou, Jue
Lai, Fritz
Leopold, Stije J.
Loo, Hooi Linn
Ghose, Aniruddha
Dutta, Ashok K.
Chen, Qingfeng
Ooi, Eng Eong
White, Nicholas J.
Dondorp, Arjen M.
Preiser, Peter
Chen, Jianzhu
format Article
author Ye, Weijian
Chew, Marvin
Hou, Jue
Lai, Fritz
Leopold, Stije J.
Loo, Hooi Linn
Ghose, Aniruddha
Dutta, Ashok K.
Chen, Qingfeng
Ooi, Eng Eong
White, Nicholas J.
Dondorp, Arjen M.
Preiser, Peter
Chen, Jianzhu
author_sort Ye, Weijian
title Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway
title_short Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway
title_full Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway
title_fullStr Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway
title_full_unstemmed Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway
title_sort microvesicles from malaria-infected red blood cells activate natural killer cells via mda5 pathway
publishDate 2019
url https://hdl.handle.net/10356/106329
http://hdl.handle.net/10220/47420
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