TY - JOUR
T1 - The Multifaceted Neurotoxicity of Astrocytes in Ageing and Age-Related Neurodegenerative Diseases
T2 - A Translational Perspective
AU - Bouvier, David S.
AU - Fixemer, Sonja
AU - Heurtaux, Tony
AU - Jeannelle, Félicia
AU - Frauenknecht, Katrin B.M.
AU - Mittelbronn, Michel
N1 - Funding Information:
DB was supported by the Luxembourg Espoir-en-Tête Rotary Club award, the Auguste et Simone Prévot foundation, and the Agaajani family donation. SF was supported by the PRIDE program of the Luxembourg National Research Found through the grant PRIDE17/12244779/PARK-QC, and FJ was supported by the AFR FNR program. MM would like to thank the Luxembourg National Research Fond (FNR) for the support (FNR PEARL P16/BM/11192868 grant).
Publisher Copyright:
Copyright © 2022 Bouvier, Fixemer, Heurtaux, Jeannelle, Frauenknecht and Mittelbronn.
PY - 2022/3/17
Y1 - 2022/3/17
N2 - In a healthy physiological context, astrocytes are multitasking cells contributing to central nervous system (CNS) homeostasis, defense, and immunity. In cell culture or rodent models of age-related neurodegenerative diseases (NDDs), such as Alzheimer’s disease (AD) and Parkinson’s disease (PD), numerous studies have shown that astrocytes can adopt neurotoxic phenotypes that could enhance disease progression. Chronic inflammatory responses, oxidative stress, unbalanced phagocytosis, or alteration of their core physiological roles are the main manifestations of their detrimental states. However, if astrocytes are directly involved in brain deterioration by exerting neurotoxic functions in patients with NDDs is still controversial. The large spectrum of NDDs, with often overlapping pathologies, and the technical challenges associated with the study of human brain samples complexify the analysis of astrocyte involvement in specific neurodegenerative cascades. With this review, we aim to provide a translational overview about the multi-facets of astrocyte neurotoxicity ranging from in vitro findings over mouse and human cell-based studies to rodent NDDs research and finally evidence from patient-related research. We also discuss the role of ageing in astrocytes encompassing changes in physiology and response to pathologic stimuli and how this may prime detrimental responses in NDDs. To conclude, we discuss how potentially therapeutic strategies could be adopted to alleviate or reverse astrocytic toxicity and their potential to impact neurodegeneration and dementia progression in patients.
AB - In a healthy physiological context, astrocytes are multitasking cells contributing to central nervous system (CNS) homeostasis, defense, and immunity. In cell culture or rodent models of age-related neurodegenerative diseases (NDDs), such as Alzheimer’s disease (AD) and Parkinson’s disease (PD), numerous studies have shown that astrocytes can adopt neurotoxic phenotypes that could enhance disease progression. Chronic inflammatory responses, oxidative stress, unbalanced phagocytosis, or alteration of their core physiological roles are the main manifestations of their detrimental states. However, if astrocytes are directly involved in brain deterioration by exerting neurotoxic functions in patients with NDDs is still controversial. The large spectrum of NDDs, with often overlapping pathologies, and the technical challenges associated with the study of human brain samples complexify the analysis of astrocyte involvement in specific neurodegenerative cascades. With this review, we aim to provide a translational overview about the multi-facets of astrocyte neurotoxicity ranging from in vitro findings over mouse and human cell-based studies to rodent NDDs research and finally evidence from patient-related research. We also discuss the role of ageing in astrocytes encompassing changes in physiology and response to pathologic stimuli and how this may prime detrimental responses in NDDs. To conclude, we discuss how potentially therapeutic strategies could be adopted to alleviate or reverse astrocytic toxicity and their potential to impact neurodegeneration and dementia progression in patients.
KW - ageing
KW - astrocyte
KW - heterogeneity
KW - neurodegeneration
KW - neurotoxicity
KW - reactive astrogliosis
UR - http://www.scopus.com/inward/record.url?scp=85127919075&partnerID=8YFLogxK
UR - https://pubmed.ncbi.nlm.nih.gov/35370777
U2 - 10.3389/fphys.2022.814889
DO - 10.3389/fphys.2022.814889
M3 - Review article
C2 - 35370777
AN - SCOPUS:85127919075
SN - 1664-042X
VL - 13
JO - Frontiers in Physiology
JF - Frontiers in Physiology
M1 - 814889
ER -