TY - JOUR
T1 - Neuroprotective and Neurotoxic Effects of Glial-Derived Exosomes
AU - Oyarce, Karina
AU - Cepeda, María Yamila
AU - Lagos, Raúl
AU - Garrido, Camila
AU - Vega-Letter, Ana María
AU - Garcia-Robles, María
AU - Luz-Crawford, Patricia
AU - Elizondo-Vega, Roberto
N1 - Funding Information:
This work was supported by grants from the Agencia Nacional de Investigación y Desarrollo-ANID; “Fondecyt iniciación” N° 11190690 (to RE-V) and “Fondecyt iniciación” N° 11190914 (to KO).
Publisher Copyright:
Copyright © 2022 Oyarce, Cepeda, Lagos, Garrido, Vega-Letter, Garcia-Robles, Luz-Crawford and Elizondo-Vega.
PY - 2022/6/22
Y1 - 2022/6/22
N2 - Exosomes derived from glial cells such as astrocytes, microglia, and oligodendrocytes can modulate cell communication in the brain and exert protective or neurotoxic effects on neurons, depending on the environmental context upon their release. Their isolation, characterization, and analysis under different conditions in vitro, in animal models and samples derived from patients has allowed to define the participation of other molecular mechanisms behind neuroinflammation and neurodegeneration spreading, and to propose their use as a potential diagnostic tool. Moreover, the discovery of specific molecular cargos, such as cytokines, membrane-bound and soluble proteins (neurotrophic factors, growth factors, misfolded proteins), miRNA and long-non-coding RNA, that are enriched in glial-derived exosomes with neuroprotective or damaging effects, or their inhibitors can now be tested as therapeutic tools. In this review we summarize the state of the art on how exosomes secretion by glia can affect neurons and other glia from the central nervous system in the context of neurodegeneration and neuroinflammation, but also, on how specific stress stimuli and pathological conditions can change the levels of exosome secretion and their properties.
AB - Exosomes derived from glial cells such as astrocytes, microglia, and oligodendrocytes can modulate cell communication in the brain and exert protective or neurotoxic effects on neurons, depending on the environmental context upon their release. Their isolation, characterization, and analysis under different conditions in vitro, in animal models and samples derived from patients has allowed to define the participation of other molecular mechanisms behind neuroinflammation and neurodegeneration spreading, and to propose their use as a potential diagnostic tool. Moreover, the discovery of specific molecular cargos, such as cytokines, membrane-bound and soluble proteins (neurotrophic factors, growth factors, misfolded proteins), miRNA and long-non-coding RNA, that are enriched in glial-derived exosomes with neuroprotective or damaging effects, or their inhibitors can now be tested as therapeutic tools. In this review we summarize the state of the art on how exosomes secretion by glia can affect neurons and other glia from the central nervous system in the context of neurodegeneration and neuroinflammation, but also, on how specific stress stimuli and pathological conditions can change the levels of exosome secretion and their properties.
KW - astrocytes
KW - exosomes
KW - microglia
KW - neuroinflammation
KW - neuroprotective
KW - neurotoxic
KW - oligodendrocyte
KW - Astrocytes
KW - Exosomes
KW - Microglia
KW - Neuroinflammation
KW - Neuroprotective
KW - Neurotoxic
KW - Oligodendrocyte
UR - http://www.scopus.com/inward/record.url?scp=85133717620&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/1bf43bfe-5c52-3e5b-b267-9fe93a08f0a7/
U2 - 10.3389/fncel.2022.920686
DO - 10.3389/fncel.2022.920686
M3 - Review article
C2 - 35813501
AN - SCOPUS:85133717620
SN - 1662-5102
VL - 16
SP - 920686
JO - Frontiers in Cellular Neuroscience
JF - Frontiers in Cellular Neuroscience
M1 - 920686
ER -