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 in | Advanced science Vol. 11; no. 41; pp. e2403389 - n/a |
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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). |
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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 – name: 4 Department of Bioinformatics School of Basic Medical Sciences Southern Medical University Guangzhou 510515 China – name: 2 Microbiome Medicine Center Department of Laboratory Medicine Zhujiang Hospital Southern Medical University Guangzhou 510260 China – name: 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 – name: 5 Department of Oncology Nanfang Hospital Southern Medical University Guangzhou 510515 China |
Author_xml | – sequence: 1 givenname: Jia‐Wen surname: Mo fullname: Mo, Jia‐Wen organization: Southern Medical University – sequence: 2 givenname: Peng‐Li surname: Kong fullname: Kong, Peng‐Li organization: Southern Medical University – sequence: 3 givenname: Li surname: Ding fullname: Ding, Li organization: Southern Medical University – sequence: 4 givenname: Jun surname: Fan fullname: Fan, Jun organization: Southern Medical University – sequence: 5 givenname: Jing surname: Ren fullname: Ren, Jing organization: Southern Medical University – sequence: 6 givenname: Cheng‐Lin surname: Lu fullname: Lu, Cheng‐Lin organization: Southern Medical University – sequence: 7 givenname: Fang surname: Guo fullname: Guo, Fang organization: Southern Medical University – sequence: 8 givenname: Liang‐Yu surname: Chen fullname: Chen, Liang‐Yu organization: Southern Medical University – sequence: 9 givenname: Ran surname: Mo fullname: Mo, Ran organization: Southern Medical University – sequence: 10 givenname: Qiu‐Ling surname: Zhong fullname: Zhong, Qiu‐Ling organization: Southern Medical University – sequence: 11 givenname: You‐Lu surname: Wen fullname: Wen, You‐Lu organization: South China Normal University – sequence: 12 givenname: Ting‐Ting surname: Gu fullname: Gu, Ting‐Ting organization: South China Normal University – sequence: 13 givenname: Qian‐Wen surname: Wang fullname: Wang, Qian‐Wen organization: Southern Medical University – sequence: 14 givenname: Shu‐Ji surname: Li fullname: Li, Shu‐Ji organization: Southern Medical University – sequence: 15 givenname: Ting surname: Guo fullname: Guo, Ting organization: Southern Medical University – sequence: 16 givenname: Tian‐Ming surname: Gao fullname: Gao, Tian‐Ming organization: Southern Medical University – sequence: 17 givenname: Xiong orcidid: 0000-0002-1889-4255 surname: Cao fullname: Cao, Xiong email: caoxiong@smu.edu.cn organization: Southern Medical University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39264289$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1038_s41467_025_57924_1 crossref_primary_10_1002_advs_202410273 |
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Keywords | transcription factor EB lysosomes astrocytes depressive‐like behaviors ATP mucolipin TRP channel 1 |
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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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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 |
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