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Endothelial TFEB signaling-mediated autophagic disturbance initiates microglial activation and cognitive dysfunction
Cognitive impairment caused by systemic chemotherapy is a critical question that perplexes the effective implementation of clinical treatment, but related molecular events are poorly understood. Herein, we show that bortezomib exposure leads to microglia activation and cognitive impairment, this occ...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262803/ https://www.ncbi.nlm.nih.gov/pubmed/36588318 http://dx.doi.org/10.1080/15548627.2022.2162244 |
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author | Lu, Yaping Chen, Xiang Liu, Xiuxiu Shi, Yi Wei, Zhaocong Feng, Lili Jiang, Quan Ye, Weifeng Sasaki, Takuya Fukunaga, Kohji Ji, Yong Han, Feng Lu, Ying-Mei |
author_facet | Lu, Yaping Chen, Xiang Liu, Xiuxiu Shi, Yi Wei, Zhaocong Feng, Lili Jiang, Quan Ye, Weifeng Sasaki, Takuya Fukunaga, Kohji Ji, Yong Han, Feng Lu, Ying-Mei |
author_sort | Lu, Yaping |
collection | PubMed |
description | Cognitive impairment caused by systemic chemotherapy is a critical question that perplexes the effective implementation of clinical treatment, but related molecular events are poorly understood. Herein, we show that bortezomib exposure leads to microglia activation and cognitive impairment, this occurs along with decreased nuclear translocation of TFEB (transcription factor EB), which is linked to macroautophagy/autophagy disorder, STAT3 (signal transducer and activator of transcription 3) phosphorylation and IL23A (interleukin 23 subunit alpha) expression. Pharmacological enhancement of TFEB nuclear translocation by digoxin restores lysosomal function and reduces STAT3-dependent endothelial IL23A secretion. As a consequence, we found that brain endothelial-specific ablation of Il23a ameliorated both microglia activation and cognitive dysfunction. Thus, the endothelial TFEB-STAT3-IL23A axis in the brain represents a critical cellular event for initiating bortezomib-mediated aberrant microglial activation and synapse engulfment. Our results suggest the reversal of TFEB nuclear translocation may provide a novel therapeutic approach to prevent symptoms of cognitive dysfunction during clinical use of bortezomib. Abbreviations: AAV: adeno-associated virus; BBB: blood-brain barrier; BTZ: bortezomib; DG: digoxin; DGs: dentate gyrus; DLG4/PSD95: discs large MAGUK scaffold protein 4; HBMECs: human brain microvascular endothelial cells; HP: hippocampus; IL23A: interleukin 23 subunit alpha; MBVECs: mouse brain vascular endothelial cells; mPFC: medial prefrontal cortex; NORT: novel object recognition test; OLT: object location test; PLX5622: 6-fluoro-N-([5-fluoro-2-methoxypyridin-3-yl]methyl)-5-(5-methyl-1H-pyrrolo[2,3-b]pyridin-3- yl)methyl; PPP3/calcineurin: protein phosphatase 3; SBEs: STAT3 binding elements; shRNA: small hairpin RNA; SLC17A7/VGLUT1: solute carrier family 17 member 7; SLC32A1/VGAT: solute carrier family 32 member 1; STAT3: signal transducer and activator of transcription 3, TFEB: transcription factor EB; Ub: ubiquitin. |
format | Online Article Text |
id | pubmed-10262803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-102628032023-06-15 Endothelial TFEB signaling-mediated autophagic disturbance initiates microglial activation and cognitive dysfunction Lu, Yaping Chen, Xiang Liu, Xiuxiu Shi, Yi Wei, Zhaocong Feng, Lili Jiang, Quan Ye, Weifeng Sasaki, Takuya Fukunaga, Kohji Ji, Yong Han, Feng Lu, Ying-Mei Autophagy Research Paper Cognitive impairment caused by systemic chemotherapy is a critical question that perplexes the effective implementation of clinical treatment, but related molecular events are poorly understood. Herein, we show that bortezomib exposure leads to microglia activation and cognitive impairment, this occurs along with decreased nuclear translocation of TFEB (transcription factor EB), which is linked to macroautophagy/autophagy disorder, STAT3 (signal transducer and activator of transcription 3) phosphorylation and IL23A (interleukin 23 subunit alpha) expression. Pharmacological enhancement of TFEB nuclear translocation by digoxin restores lysosomal function and reduces STAT3-dependent endothelial IL23A secretion. As a consequence, we found that brain endothelial-specific ablation of Il23a ameliorated both microglia activation and cognitive dysfunction. Thus, the endothelial TFEB-STAT3-IL23A axis in the brain represents a critical cellular event for initiating bortezomib-mediated aberrant microglial activation and synapse engulfment. Our results suggest the reversal of TFEB nuclear translocation may provide a novel therapeutic approach to prevent symptoms of cognitive dysfunction during clinical use of bortezomib. Abbreviations: AAV: adeno-associated virus; BBB: blood-brain barrier; BTZ: bortezomib; DG: digoxin; DGs: dentate gyrus; DLG4/PSD95: discs large MAGUK scaffold protein 4; HBMECs: human brain microvascular endothelial cells; HP: hippocampus; IL23A: interleukin 23 subunit alpha; MBVECs: mouse brain vascular endothelial cells; mPFC: medial prefrontal cortex; NORT: novel object recognition test; OLT: object location test; PLX5622: 6-fluoro-N-([5-fluoro-2-methoxypyridin-3-yl]methyl)-5-(5-methyl-1H-pyrrolo[2,3-b]pyridin-3- yl)methyl; PPP3/calcineurin: protein phosphatase 3; SBEs: STAT3 binding elements; shRNA: small hairpin RNA; SLC17A7/VGLUT1: solute carrier family 17 member 7; SLC32A1/VGAT: solute carrier family 32 member 1; STAT3: signal transducer and activator of transcription 3, TFEB: transcription factor EB; Ub: ubiquitin. Taylor & Francis 2023-01-01 /pmc/articles/PMC10262803/ /pubmed/36588318 http://dx.doi.org/10.1080/15548627.2022.2162244 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Research Paper Lu, Yaping Chen, Xiang Liu, Xiuxiu Shi, Yi Wei, Zhaocong Feng, Lili Jiang, Quan Ye, Weifeng Sasaki, Takuya Fukunaga, Kohji Ji, Yong Han, Feng Lu, Ying-Mei Endothelial TFEB signaling-mediated autophagic disturbance initiates microglial activation and cognitive dysfunction |
title | Endothelial TFEB signaling-mediated autophagic disturbance initiates microglial activation and cognitive dysfunction |
title_full | Endothelial TFEB signaling-mediated autophagic disturbance initiates microglial activation and cognitive dysfunction |
title_fullStr | Endothelial TFEB signaling-mediated autophagic disturbance initiates microglial activation and cognitive dysfunction |
title_full_unstemmed | Endothelial TFEB signaling-mediated autophagic disturbance initiates microglial activation and cognitive dysfunction |
title_short | Endothelial TFEB signaling-mediated autophagic disturbance initiates microglial activation and cognitive dysfunction |
title_sort | endothelial tfeb signaling-mediated autophagic disturbance initiates microglial activation and cognitive dysfunction |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262803/ https://www.ncbi.nlm.nih.gov/pubmed/36588318 http://dx.doi.org/10.1080/15548627.2022.2162244 |
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