Baeke, Femke

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  • Baeke, Femke (1)
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Importance of extracellular vesicle secretion at the blood-cerebrospinal fluid interface in the pathogenesis of Alzheimer's disease.

Vandendriessche, Charysse; Balusu, Sriram; Van Cauwenberghe, Caroline; Brkić, Marjana; Pauwels, Marie; Plehiers, Nele; Bruggeman, Arnout; Dujardin, Pieter; Van Imschoot, Griet; Van Wonterghem, Elien; Hendrix, An; Baeke, Femke; De Rycke, Riet; Gevaert, Kris; Vandenbroucke, Roosmarijn E.

(2021)

TY  - JOUR
AU  - Vandendriessche, Charysse
AU  - Balusu, Sriram
AU  - Van Cauwenberghe, Caroline
AU  - Brkić, Marjana
AU  - Pauwels, Marie
AU  - Plehiers, Nele
AU  - Bruggeman, Arnout
AU  - Dujardin, Pieter
AU  - Van Imschoot, Griet
AU  - Van Wonterghem, Elien
AU  - Hendrix, An
AU  - Baeke, Femke
AU  - De Rycke, Riet
AU  - Gevaert, Kris
AU  - Vandenbroucke, Roosmarijn E.
PY  - 2021
UR  - https://actaneurocomms.biomedcentral.com/articles/10.1186/s40478-021-01245-z
UR  - http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=PMC8381545
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/4476
AB  - Increasing evidence indicates that extracellular vesicles (EVs) play an important role in the pathogenesis of Alzheimer's disease (AD). We previously reported that the blood-cerebrospinal fluid (CSF) interface, formed by the choroid plexus epithelial (CPE) cells, releases an increased amount of EVs into the CSF in response to peripheral inflammation. Here, we studied the importance of CP-mediated EV release in AD pathogenesis. We observed increased EV levels in the CSF of young transgenic APP/PS1 mice which correlated with high amyloid beta (Aβ) CSF levels at this age. The intracerebroventricular (icv) injection of Aβ oligomers (AβO) in wild-type mice revealed a significant increase of EVs in the CSF, signifying that the presence of CSF-AβO is sufficient to induce increased EV secretion. Using in vivo, in vitro and ex vivo approaches, we identified the CP as a major source of the CSF-EVs. Interestingly, AβO-induced, CP-derived EVs induced pro-inflammatory effects in mixed cortical cultures. Proteome analysis of these EVs revealed the presence of several pro-inflammatory proteins, including the complement protein C3. Strikingly, inhibition of EV production using GW4869 resulted in protection against acute AβO-induced cognitive decline. Further research into the underlying mechanisms of this EV secretion might open up novel therapeutic strategies to impact the pathogenesis and progression of AD.
T2  - Acta Neuropathologica Communications
T1  - Importance of extracellular vesicle secretion at the blood-cerebrospinal fluid interface in the pathogenesis of Alzheimer's disease.
IS  - 1
VL  - 9
DO  - 10.1186/s40478-021-01245-z
SP  - 143
ER  - 
@article{
author = "Vandendriessche, Charysse and Balusu, Sriram and Van Cauwenberghe, Caroline and Brkić, Marjana and Pauwels, Marie and Plehiers, Nele and Bruggeman, Arnout and Dujardin, Pieter and Van Imschoot, Griet and Van Wonterghem, Elien and Hendrix, An and Baeke, Femke and De Rycke, Riet and Gevaert, Kris and Vandenbroucke, Roosmarijn E.",
year = "2021",
abstract = "Increasing evidence indicates that extracellular vesicles (EVs) play an important role in the pathogenesis of Alzheimer's disease (AD). We previously reported that the blood-cerebrospinal fluid (CSF) interface, formed by the choroid plexus epithelial (CPE) cells, releases an increased amount of EVs into the CSF in response to peripheral inflammation. Here, we studied the importance of CP-mediated EV release in AD pathogenesis. We observed increased EV levels in the CSF of young transgenic APP/PS1 mice which correlated with high amyloid beta (Aβ) CSF levels at this age. The intracerebroventricular (icv) injection of Aβ oligomers (AβO) in wild-type mice revealed a significant increase of EVs in the CSF, signifying that the presence of CSF-AβO is sufficient to induce increased EV secretion. Using in vivo, in vitro and ex vivo approaches, we identified the CP as a major source of the CSF-EVs. Interestingly, AβO-induced, CP-derived EVs induced pro-inflammatory effects in mixed cortical cultures. Proteome analysis of these EVs revealed the presence of several pro-inflammatory proteins, including the complement protein C3. Strikingly, inhibition of EV production using GW4869 resulted in protection against acute AβO-induced cognitive decline. Further research into the underlying mechanisms of this EV secretion might open up novel therapeutic strategies to impact the pathogenesis and progression of AD.",
journal = "Acta Neuropathologica Communications",
title = "Importance of extracellular vesicle secretion at the blood-cerebrospinal fluid interface in the pathogenesis of Alzheimer's disease.",
number = "1",
volume = "9",
doi = "10.1186/s40478-021-01245-z",
pages = "143"
}
Vandendriessche, C., Balusu, S., Van Cauwenberghe, C., Brkić, M., Pauwels, M., Plehiers, N., Bruggeman, A., Dujardin, P., Van Imschoot, G., Van Wonterghem, E., Hendrix, A., Baeke, F., De Rycke, R., Gevaert, K.,& Vandenbroucke, R. E.. (2021). Importance of extracellular vesicle secretion at the blood-cerebrospinal fluid interface in the pathogenesis of Alzheimer's disease.. in Acta Neuropathologica Communications, 9(1), 143.
https://doi.org/10.1186/s40478-021-01245-z
Vandendriessche C, Balusu S, Van Cauwenberghe C, Brkić M, Pauwels M, Plehiers N, Bruggeman A, Dujardin P, Van Imschoot G, Van Wonterghem E, Hendrix A, Baeke F, De Rycke R, Gevaert K, Vandenbroucke RE. Importance of extracellular vesicle secretion at the blood-cerebrospinal fluid interface in the pathogenesis of Alzheimer's disease.. in Acta Neuropathologica Communications. 2021;9(1):143.
doi:10.1186/s40478-021-01245-z .
Vandendriessche, Charysse, Balusu, Sriram, Van Cauwenberghe, Caroline, Brkić, Marjana, Pauwels, Marie, Plehiers, Nele, Bruggeman, Arnout, Dujardin, Pieter, Van Imschoot, Griet, Van Wonterghem, Elien, Hendrix, An, Baeke, Femke, De Rycke, Riet, Gevaert, Kris, Vandenbroucke, Roosmarijn E., "Importance of extracellular vesicle secretion at the blood-cerebrospinal fluid interface in the pathogenesis of Alzheimer's disease." in Acta Neuropathologica Communications, 9, no. 1 (2021):143,
https://doi.org/10.1186/s40478-021-01245-z . .
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