Lysosomal TFEB‐TRPML1 Axis in Astrocytes Modulates Depressive‐like Behaviors

Lysosomes are important cellular structures for human health as centers for recycling, signaling, metabolism and stress adaptation. However, the potential role of lysosomes in stress‐related emotions has long been overlooked. Here, it is found that lysosomal morphology in astrocytes is altered in th...

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Published inAdvanced science Vol. 11; no. 41; pp. e2403389 - n/a
Main Authors Mo, Jia‐Wen, Kong, Peng‐Li, Ding, Li, Fan, Jun, Ren, Jing, Lu, Cheng‐Lin, Guo, Fang, Chen, Liang‐Yu, Mo, Ran, Zhong, Qiu‐Ling, Wen, You‐Lu, Gu, Ting‐Ting, Wang, Qian‐Wen, Li, Shu‐Ji, Guo, Ting, Gao, Tian‐Ming, Cao, Xiong
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Published Germany John Wiley & Sons, Inc 01.11.2024
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Abstract Lysosomes are important cellular structures for human health as centers for recycling, signaling, metabolism and stress adaptation. However, the potential role of lysosomes in stress‐related emotions has long been overlooked. Here, it is found that lysosomal morphology in astrocytes is altered in the medial prefrontal cortex (mPFC) of susceptible mice after chronic social defeat stress. A screen of lysosome‐related genes revealed that the expression of the mucolipin 1 gene (Mcoln1; protein: mucolipin TRP channel 1) is decreased in susceptible mice and depressed patients. Astrocyte‐specific knockout of mucolipin TRP channel 1 (TRPML1) induced depressive‐like behaviors by inhibiting lysosomal exocytosis‐mediated adenosine 5′‐triphosphate (ATP) release. Furthermore, this stress response of astrocytic lysosomes is mediated by the transcription factor EB (TFEB), and overexpression of TRPML1 rescued depressive‐like behaviors induced by astrocyte‐specific knockout of TFEB. Collectively, these findings reveal a lysosomal stress‐sensing signaling pathway contributing to the development of depression and identify the lysosome as a potential target organelle for antidepressants. This study indicates that chronic stress alters the morphology of astrocytic lysosomes and the mucolipin TRP channel 1 (TRPML1) expression in the mPFC of susceptible mice. Astrocyte‐specific knockout of TRPML1 results in depressive‐like behaviors in mice by inhibiting lysosomal exocytosis‐mediated adenosine 5'‐triphosphate (ATP) release. This stress response of astrocytic lysosomes is mediated by the transcription factor EB (TFEB).
AbstractList Abstract Lysosomes are important cellular structures for human health as centers for recycling, signaling, metabolism and stress adaptation. However, the potential role of lysosomes in stress‐related emotions has long been overlooked. Here, it is found that lysosomal morphology in astrocytes is altered in the medial prefrontal cortex (mPFC) of susceptible mice after chronic social defeat stress. A screen of lysosome‐related genes revealed that the expression of the mucolipin 1 gene (Mcoln1; protein: mucolipin TRP channel 1) is decreased in susceptible mice and depressed patients. Astrocyte‐specific knockout of mucolipin TRP channel 1 (TRPML1) induced depressive‐like behaviors by inhibiting lysosomal exocytosis‐mediated adenosine 5′‐triphosphate (ATP) release. Furthermore, this stress response of astrocytic lysosomes is mediated by the transcription factor EB (TFEB), and overexpression of TRPML1 rescued depressive‐like behaviors induced by astrocyte‐specific knockout of TFEB. Collectively, these findings reveal a lysosomal stress‐sensing signaling pathway contributing to the development of depression and identify the lysosome as a potential target organelle for antidepressants.
Lysosomes are important cellular structures for human health as centers for recycling, signaling, metabolism and stress adaptation. However, the potential role of lysosomes in stress‐related emotions has long been overlooked. Here, it is found that lysosomal morphology in astrocytes is altered in the medial prefrontal cortex (mPFC) of susceptible mice after chronic social defeat stress. A screen of lysosome‐related genes revealed that the expression of the mucolipin 1 gene ( Mcoln1 ; protein: mucolipin TRP channel 1) is decreased in susceptible mice and depressed patients. Astrocyte‐specific knockout of mucolipin TRP channel 1 (TRPML1) induced depressive‐like behaviors by inhibiting lysosomal exocytosis‐mediated adenosine 5′‐triphosphate (ATP) release. Furthermore, this stress response of astrocytic lysosomes is mediated by the transcription factor EB (TFEB), and overexpression of TRPML1 rescued depressive‐like behaviors induced by astrocyte‐specific knockout of TFEB. Collectively, these findings reveal a lysosomal stress‐sensing signaling pathway contributing to the development of depression and identify the lysosome as a potential target organelle for antidepressants. This study indicates that chronic stress alters the morphology of astrocytic lysosomes and the mucolipin TRP channel 1 (TRPML1) expression in the mPFC of susceptible mice. Astrocyte‐specific knockout of TRPML1 results in depressive‐like behaviors in mice by inhibiting lysosomal exocytosis‐mediated adenosine 5'‐triphosphate (ATP) release. This stress response of astrocytic lysosomes is mediated by the transcription factor EB (TFEB).
Lysosomes are important cellular structures for human health as centers for recycling, signaling, metabolism and stress adaptation. However, the potential role of lysosomes in stress-related emotions has long been overlooked. Here, it is found that lysosomal morphology in astrocytes is altered in the medial prefrontal cortex (mPFC) of susceptible mice after chronic social defeat stress. A screen of lysosome-related genes revealed that the expression of the mucolipin 1 gene (Mcoln1; protein: mucolipin TRP channel 1) is decreased in susceptible mice and depressed patients. Astrocyte-specific knockout of mucolipin TRP channel 1 (TRPML1) induced depressive-like behaviors by inhibiting lysosomal exocytosis-mediated adenosine 5'-triphosphate (ATP) release. Furthermore, this stress response of astrocytic lysosomes is mediated by the transcription factor EB (TFEB), and overexpression of TRPML1 rescued depressive-like behaviors induced by astrocyte-specific knockout of TFEB. Collectively, these findings reveal a lysosomal stress-sensing signaling pathway contributing to the development of depression and identify the lysosome as a potential target organelle for antidepressants.Lysosomes are important cellular structures for human health as centers for recycling, signaling, metabolism and stress adaptation. However, the potential role of lysosomes in stress-related emotions has long been overlooked. Here, it is found that lysosomal morphology in astrocytes is altered in the medial prefrontal cortex (mPFC) of susceptible mice after chronic social defeat stress. A screen of lysosome-related genes revealed that the expression of the mucolipin 1 gene (Mcoln1; protein: mucolipin TRP channel 1) is decreased in susceptible mice and depressed patients. Astrocyte-specific knockout of mucolipin TRP channel 1 (TRPML1) induced depressive-like behaviors by inhibiting lysosomal exocytosis-mediated adenosine 5'-triphosphate (ATP) release. Furthermore, this stress response of astrocytic lysosomes is mediated by the transcription factor EB (TFEB), and overexpression of TRPML1 rescued depressive-like behaviors induced by astrocyte-specific knockout of TFEB. Collectively, these findings reveal a lysosomal stress-sensing signaling pathway contributing to the development of depression and identify the lysosome as a potential target organelle for antidepressants.
Lysosomes are important cellular structures for human health as centers for recycling, signaling, metabolism and stress adaptation. However, the potential role of lysosomes in stress-related emotions has long been overlooked. Here, it is found that lysosomal morphology in astrocytes is altered in the medial prefrontal cortex (mPFC) of susceptible mice after chronic social defeat stress. A screen of lysosome-related genes revealed that the expression of the mucolipin 1 gene (Mcoln1; protein: mucolipin TRP channel 1) is decreased in susceptible mice and depressed patients. Astrocyte-specific knockout of mucolipin TRP channel 1 (TRPML1) induced depressive-like behaviors by inhibiting lysosomal exocytosis-mediated adenosine 5'-triphosphate (ATP) release. Furthermore, this stress response of astrocytic lysosomes is mediated by the transcription factor EB (TFEB), and overexpression of TRPML1 rescued depressive-like behaviors induced by astrocyte-specific knockout of TFEB. Collectively, these findings reveal a lysosomal stress-sensing signaling pathway contributing to the development of depression and identify the lysosome as a potential target organelle for antidepressants.
Lysosomes are important cellular structures for human health as centers for recycling, signaling, metabolism and stress adaptation. However, the potential role of lysosomes in stress‐related emotions has long been overlooked. Here, it is found that lysosomal morphology in astrocytes is altered in the medial prefrontal cortex (mPFC) of susceptible mice after chronic social defeat stress. A screen of lysosome‐related genes revealed that the expression of the mucolipin 1 gene (Mcoln1; protein: mucolipin TRP channel 1) is decreased in susceptible mice and depressed patients. Astrocyte‐specific knockout of mucolipin TRP channel 1 (TRPML1) induced depressive‐like behaviors by inhibiting lysosomal exocytosis‐mediated adenosine 5′‐triphosphate (ATP) release. Furthermore, this stress response of astrocytic lysosomes is mediated by the transcription factor EB (TFEB), and overexpression of TRPML1 rescued depressive‐like behaviors induced by astrocyte‐specific knockout of TFEB. Collectively, these findings reveal a lysosomal stress‐sensing signaling pathway contributing to the development of depression and identify the lysosome as a potential target organelle for antidepressants. This study indicates that chronic stress alters the morphology of astrocytic lysosomes and the mucolipin TRP channel 1 (TRPML1) expression in the mPFC of susceptible mice. Astrocyte‐specific knockout of TRPML1 results in depressive‐like behaviors in mice by inhibiting lysosomal exocytosis‐mediated adenosine 5'‐triphosphate (ATP) release. This stress response of astrocytic lysosomes is mediated by the transcription factor EB (TFEB).
Author Chen, Liang‐Yu
Fan, Jun
Li, Shu‐Ji
Kong, Peng‐Li
Zhong, Qiu‐Ling
Ren, Jing
Mo, Ran
Wang, Qian‐Wen
Cao, Xiong
Wen, You‐Lu
Gu, Ting‐Ting
Mo, Jia‐Wen
Guo, Ting
Guo, Fang
Gao, Tian‐Ming
Ding, Li
Lu, Cheng‐Lin
AuthorAffiliation 2 Microbiome Medicine Center Department of Laboratory Medicine Zhujiang Hospital Southern Medical University Guangzhou 510260 China
1 Key Laboratory of Mental Health of the Ministry of Education Guangdong‐Hong Kong‐Macao Greater Bay Area Center for Brain Science and Brain‐Inspired Intelligence Guangdong‐Hong Kong Joint Laboratory for Psychiatric Disorders Guangdong Province Key Laboratory of Psychiatric Disorders Guangdong Basic Research Center of Excellence for Integrated Traditional and Western Medicine for Qingzhi Diseases Department of Neurobiology School of Basic Medical Sciences Southern Medical University Guangzhou 510515 China
4 Department of Bioinformatics School of Basic Medical Sciences Southern Medical University Guangzhou 510515 China
5 Department of Oncology Nanfang Hospital Southern Medical University Guangzhou 510515 China
3 Department of Psychology and Behavior Guangdong 999 Brain Hospital Institute for Brain Research and Rehabilitation South China Normal University Guangz
AuthorAffiliation_xml – name: 3 Department of Psychology and Behavior Guangdong 999 Brain Hospital Institute for Brain Research and Rehabilitation South China Normal University Guangzhou 510515 China
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– name: 2 Microbiome Medicine Center Department of Laboratory Medicine Zhujiang Hospital Southern Medical University Guangzhou 510260 China
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– name: 5 Department of Oncology Nanfang Hospital Southern Medical University Guangzhou 510515 China
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Keywords transcription factor EB
lysosomes
astrocytes
depressive‐like behaviors
ATP
mucolipin TRP channel 1
Language English
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Wiley
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SSID ssj0001537418
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Snippet Lysosomes are important cellular structures for human health as centers for recycling, signaling, metabolism and stress adaptation. However, the potential role...
Abstract Lysosomes are important cellular structures for human health as centers for recycling, signaling, metabolism and stress adaptation. However, the...
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pubmedcentral
proquest
pubmed
crossref
wiley
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage e2403389
SubjectTerms Animals
astrocytes
Astrocytes - metabolism
ATP
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - genetics
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism
Behavior, Animal
Brain
Depression - genetics
Depression - metabolism
depressive‐like behaviors
Disease Models, Animal
Humans
lysosomes
Lysosomes - metabolism
Male
Mental depression
Mice
Mice, Inbred C57BL
Mice, Knockout
Microscopy
Morphology
mucolipin TRP channel 1
Neurons
Prefrontal Cortex - metabolism
Proteins
Quantitative analysis
Signal Transduction - genetics
Stress
transcription factor EB
Transient Receptor Potential Channels - genetics
Transient Receptor Potential Channels - metabolism
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Title Lysosomal TFEB‐TRPML1 Axis in Astrocytes Modulates Depressive‐like Behaviors
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fadvs.202403389
https://www.ncbi.nlm.nih.gov/pubmed/39264289
https://www.proquest.com/docview/3124286096
https://www.proquest.com/docview/3103451027
https://pubmed.ncbi.nlm.nih.gov/PMC11538709
https://doaj.org/article/1cd74eec8301438b9b272bb2dbafc826
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