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Role of astrocyte senescence regulated by the non– canonical autophagy in the neuroinflammation associated to cerebral malaria

•Cellular senescence and resistance to apoptosis are observed in Astrocytes during cerebral malaria in mice and humans.•Astrocyte senescence is triggered by LC3-dependent non-conventional autophagy when interacting with the malaria parasite.•Parasite-induced senescence promotes the production of CX-...

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Published in:Brain, behavior, and immunity behavior, and immunity, 2024-03, Vol.117, p.20-35
Main Authors: Hellani, Fatima, Leleu, Inès, Saidi, Nasreddine, Martin, Nathalie, Lecoeur, Cécile, Werkmeister, Elisabeth, Koffi, David, Trottein, François, Yapo-Etté, Hélène, Das, Bidyut, Abbadie, Corinne, Pied, Sylviane
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container_title Brain, behavior, and immunity
container_volume 117
creator Hellani, Fatima
Leleu, Inès
Saidi, Nasreddine
Martin, Nathalie
Lecoeur, Cécile
Werkmeister, Elisabeth
Koffi, David
Trottein, François
Yapo-Etté, Hélène
Das, Bidyut
Abbadie, Corinne
Pied, Sylviane
description •Cellular senescence and resistance to apoptosis are observed in Astrocytes during cerebral malaria in mice and humans.•Astrocyte senescence is triggered by LC3-dependent non-conventional autophagy when interacting with the malaria parasite.•Parasite-induced senescence promotes the production of CX-CL10 by astrocytes.•Treatment with senolytic drugs prevents CM by reducing the inflammatory response. Cerebral malaria (CM) is a fatal neuroinflammatory syndrome caused (in humans) by the protozoa Plasmodium (P.) falciparum. Glial cell activation is one of the mechanisms that contributes to neuroinflammation in CM. By studying a mouse model of CM (caused by P. berghei ANKA), we describe that the induction of autophagy promoted p21-dependent senescence in astrocytes and that CXCL-10 was part of the senescence-associated secretory phenotype. Furthermore, p21 expression was observed in post-mortem brain and peripheral blood samples from patients with CM. Lastly, we found that the depletion of senescent astrocytes with senolytic drugs abrogated inflammation and protected mice from CM. Our data provide evidence for a novel mechanism through which astrocytes could be involved in the neuropathophysiology of CM. p21 gene expression in blood cell and an elevated plasma CXCL-10 concentration could be valuable biomarkers of CM in humans. In the end, we believe senolytic drugs shall open up new avenues to develop newer treatment options.
doi_str_mv 10.1016/j.bbi.2023.12.030
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Cerebral malaria (CM) is a fatal neuroinflammatory syndrome caused (in humans) by the protozoa Plasmodium (P.) falciparum. Glial cell activation is one of the mechanisms that contributes to neuroinflammation in CM. By studying a mouse model of CM (caused by P. berghei ANKA), we describe that the induction of autophagy promoted p21-dependent senescence in astrocytes and that CXCL-10 was part of the senescence-associated secretory phenotype. Furthermore, p21 expression was observed in post-mortem brain and peripheral blood samples from patients with CM. Lastly, we found that the depletion of senescent astrocytes with senolytic drugs abrogated inflammation and protected mice from CM. Our data provide evidence for a novel mechanism through which astrocytes could be involved in the neuropathophysiology of CM. p21 gene expression in blood cell and an elevated plasma CXCL-10 concentration could be valuable biomarkers of CM in humans. 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subjects Astrocyte
Cellular senescence
Cerebral malaria
Inflammation
Life Sciences
P21
Senolytic drugs
title Role of astrocyte senescence regulated by the non– canonical autophagy in the neuroinflammation associated to cerebral malaria
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