The macrophage-specific V-ATPase subunit ATP6V0D2 restricts inflammasome activation and bacterial infection by facilitating autophagosome-lysosome fusion

Macroautophagy/autophagy is a conserved ubiquitous pathway that performs diverse roles in health and disease. Although many key, widely expressed proteins that regulate autophagosome formation followed by lysosomal fusion have been identified, the possibilities of cell-specific elements that contrib...

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Veröffentlicht in:Autophagy 2019-06, Vol.15 (6), p.960-975
Hauptverfasser: Xia, Yu, Liu, Na, Xie, Xiuxiu, Bi, Guoyu, Ba, Hongping, Li, Lin, Zhang, Jinxia, Deng, Xiaofei, Yao, Yao, Tang, Zhaohui, Yin, Binjiao, Wang, Jing, Jiang, Kan, Li, Zhuoya, Choi, Yongwon, Gong, Feili, Cheng, Xiang, O'Shea, John J, Chae, Jae Jin, Laurence, Arian, Yang, Xiang-Ping
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container_end_page 975
container_issue 6
container_start_page 960
container_title Autophagy
container_volume 15
creator Xia, Yu
Liu, Na
Xie, Xiuxiu
Bi, Guoyu
Ba, Hongping
Li, Lin
Zhang, Jinxia
Deng, Xiaofei
Yao, Yao
Tang, Zhaohui
Yin, Binjiao
Wang, Jing
Jiang, Kan
Li, Zhuoya
Choi, Yongwon
Gong, Feili
Cheng, Xiang
O'Shea, John J
Chae, Jae Jin
Laurence, Arian
Yang, Xiang-Ping
description Macroautophagy/autophagy is a conserved ubiquitous pathway that performs diverse roles in health and disease. Although many key, widely expressed proteins that regulate autophagosome formation followed by lysosomal fusion have been identified, the possibilities of cell-specific elements that contribute to the autophagy fusion machinery have not been explored. Here we show that a macrophage-specific isoform of the vacuolar ATPase protein ATP6V0D2/subunit d2 is dispensable for lysosome acidification, but promotes the completion of autophagy via promotion of autophagosome-lysosome fusion through its interaction with STX17 and VAMP8. Atp6v0d2-deficient macrophages have augmented mitochondrial damage, enhanced inflammasome activation and reduced clearance of Salmonella typhimurium. The susceptibility of atp6v0d2 knockout mice to DSS-induced colitis and Salmonella typhimurium-induced death, highlights the in vivo significance of ATP6V0D2-mediated autophagosome-lysosome fusion. Together, our data identify ATP6V0D2 as a key component of macrophage-specific autophagosome-lysosome fusion machinery maintaining macrophage organelle homeostasis and, in turn, limiting both inflammation and bacterial infection. Abbreviations: ACTB/β-actin: actin, beta; ATG14: autophagy related 14; ATG16L1: autophagy related 16-like 1 (S. cerevisiae); ATP6V0D1/2: ATPase, H+ transporting, lysosomal V0 subunit D1/2; AIM2: absent in melanoma 2; BMDM: bone marrow-derived macrophage; CASP1: caspase 1; CGD: chronic granulomatous disease; CSF1/M-CSF: colony stimulating factor 1 (macrophage); CTSB: cathepsin B; DSS: dextran sodium sulfate; IL1B: interleukin 1 beta; IL6: interleukin 6; IRGM: immunity-related GTPase family M member; KO: knockout; LAMP1: lysosomal-associated membrane protein 1; LC3: microtubule-associated protein 1 light chain 3; LPS: lipo-polysaccaride; NLRP3: NLR family, pyrin domain containing 3; PYCARD/ASC: PYD and CARD domain containing; SNARE: soluble N-ethylmaleimide-sensitive factor attachment protein receptor; SNAP29: synaptosomal-associated protein 29; SQSTM1/p62: sequestosome 1; STX17: syntaxin 17; TLR: toll-like receptor; TNF: tumor necrosis factor ; TOMM20: translocase of outer mitochondrial membrane 20; ULK1: unc-51 like kinase 1; VAMP8: vesicle-associated membrane protein 8; WT: wild type; 3-MA: 3-methyladenine
doi_str_mv 10.1080/15548627.2019.1569916
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Although many key, widely expressed proteins that regulate autophagosome formation followed by lysosomal fusion have been identified, the possibilities of cell-specific elements that contribute to the autophagy fusion machinery have not been explored. Here we show that a macrophage-specific isoform of the vacuolar ATPase protein ATP6V0D2/subunit d2 is dispensable for lysosome acidification, but promotes the completion of autophagy via promotion of autophagosome-lysosome fusion through its interaction with STX17 and VAMP8. Atp6v0d2-deficient macrophages have augmented mitochondrial damage, enhanced inflammasome activation and reduced clearance of Salmonella typhimurium. The susceptibility of atp6v0d2 knockout mice to DSS-induced colitis and Salmonella typhimurium-induced death, highlights the in vivo significance of ATP6V0D2-mediated autophagosome-lysosome fusion. Together, our data identify ATP6V0D2 as a key component of macrophage-specific autophagosome-lysosome fusion machinery maintaining macrophage organelle homeostasis and, in turn, limiting both inflammation and bacterial infection. Abbreviations: ACTB/β-actin: actin, beta; ATG14: autophagy related 14; ATG16L1: autophagy related 16-like 1 (S. cerevisiae); ATP6V0D1/2: ATPase, H+ transporting, lysosomal V0 subunit D1/2; AIM2: absent in melanoma 2; BMDM: bone marrow-derived macrophage; CASP1: caspase 1; CGD: chronic granulomatous disease; CSF1/M-CSF: colony stimulating factor 1 (macrophage); CTSB: cathepsin B; DSS: dextran sodium sulfate; IL1B: interleukin 1 beta; IL6: interleukin 6; IRGM: immunity-related GTPase family M member; KO: knockout; LAMP1: lysosomal-associated membrane protein 1; LC3: microtubule-associated protein 1 light chain 3; LPS: lipo-polysaccaride; NLRP3: NLR family, pyrin domain containing 3; PYCARD/ASC: PYD and CARD domain containing; SNARE: soluble N-ethylmaleimide-sensitive factor attachment protein receptor; SNAP29: synaptosomal-associated protein 29; SQSTM1/p62: sequestosome 1; STX17: syntaxin 17; TLR: toll-like receptor; TNF: tumor necrosis factor ; TOMM20: translocase of outer mitochondrial membrane 20; ULK1: unc-51 like kinase 1; VAMP8: vesicle-associated membrane protein 8; WT: wild type; 3-MA: 3-methyladenine</description><identifier>ISSN: 1554-8627</identifier><identifier>EISSN: 1554-8635</identifier><identifier>DOI: 10.1080/15548627.2019.1569916</identifier><identifier>PMID: 30681394</identifier><language>eng</language><publisher>United States: Taylor &amp; Francis</publisher><subject>ATP6V0D2 ; autophagosome-lysosome fusion ; IL1B ; inflammasome activation ; Research Paper ; Salmonella typhimurium</subject><ispartof>Autophagy, 2019-06, Vol.15 (6), p.960-975</ispartof><rights>2019 Huazhong University of Science and Technology 2019</rights><rights>2019 Huazhong University of Science and Technology 2019 Huazhong University of Science and Technology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c560t-a0ee4f0013843c3f30b089f82f1199d342a49cde9cf969c07ea5be142900b5723</citedby><cites>FETCH-LOGICAL-c560t-a0ee4f0013843c3f30b089f82f1199d342a49cde9cf969c07ea5be142900b5723</cites><orcidid>0000-0003-0942-8292 ; 0000-0001-9003-1772</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6526827/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6526827/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30681394$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xia, Yu</creatorcontrib><creatorcontrib>Liu, Na</creatorcontrib><creatorcontrib>Xie, Xiuxiu</creatorcontrib><creatorcontrib>Bi, Guoyu</creatorcontrib><creatorcontrib>Ba, Hongping</creatorcontrib><creatorcontrib>Li, Lin</creatorcontrib><creatorcontrib>Zhang, Jinxia</creatorcontrib><creatorcontrib>Deng, Xiaofei</creatorcontrib><creatorcontrib>Yao, Yao</creatorcontrib><creatorcontrib>Tang, Zhaohui</creatorcontrib><creatorcontrib>Yin, Binjiao</creatorcontrib><creatorcontrib>Wang, Jing</creatorcontrib><creatorcontrib>Jiang, Kan</creatorcontrib><creatorcontrib>Li, Zhuoya</creatorcontrib><creatorcontrib>Choi, Yongwon</creatorcontrib><creatorcontrib>Gong, Feili</creatorcontrib><creatorcontrib>Cheng, Xiang</creatorcontrib><creatorcontrib>O'Shea, John J</creatorcontrib><creatorcontrib>Chae, Jae Jin</creatorcontrib><creatorcontrib>Laurence, Arian</creatorcontrib><creatorcontrib>Yang, Xiang-Ping</creatorcontrib><title>The macrophage-specific V-ATPase subunit ATP6V0D2 restricts inflammasome activation and bacterial infection by facilitating autophagosome-lysosome fusion</title><title>Autophagy</title><addtitle>Autophagy</addtitle><description>Macroautophagy/autophagy is a conserved ubiquitous pathway that performs diverse roles in health and disease. Although many key, widely expressed proteins that regulate autophagosome formation followed by lysosomal fusion have been identified, the possibilities of cell-specific elements that contribute to the autophagy fusion machinery have not been explored. Here we show that a macrophage-specific isoform of the vacuolar ATPase protein ATP6V0D2/subunit d2 is dispensable for lysosome acidification, but promotes the completion of autophagy via promotion of autophagosome-lysosome fusion through its interaction with STX17 and VAMP8. Atp6v0d2-deficient macrophages have augmented mitochondrial damage, enhanced inflammasome activation and reduced clearance of Salmonella typhimurium. The susceptibility of atp6v0d2 knockout mice to DSS-induced colitis and Salmonella typhimurium-induced death, highlights the in vivo significance of ATP6V0D2-mediated autophagosome-lysosome fusion. Together, our data identify ATP6V0D2 as a key component of macrophage-specific autophagosome-lysosome fusion machinery maintaining macrophage organelle homeostasis and, in turn, limiting both inflammation and bacterial infection. Abbreviations: ACTB/β-actin: actin, beta; ATG14: autophagy related 14; ATG16L1: autophagy related 16-like 1 (S. cerevisiae); ATP6V0D1/2: ATPase, H+ transporting, lysosomal V0 subunit D1/2; AIM2: absent in melanoma 2; BMDM: bone marrow-derived macrophage; CASP1: caspase 1; CGD: chronic granulomatous disease; CSF1/M-CSF: colony stimulating factor 1 (macrophage); CTSB: cathepsin B; DSS: dextran sodium sulfate; IL1B: interleukin 1 beta; IL6: interleukin 6; IRGM: immunity-related GTPase family M member; KO: knockout; LAMP1: lysosomal-associated membrane protein 1; LC3: microtubule-associated protein 1 light chain 3; LPS: lipo-polysaccaride; NLRP3: NLR family, pyrin domain containing 3; PYCARD/ASC: PYD and CARD domain containing; SNARE: soluble N-ethylmaleimide-sensitive factor attachment protein receptor; SNAP29: synaptosomal-associated protein 29; SQSTM1/p62: sequestosome 1; STX17: syntaxin 17; TLR: toll-like receptor; TNF: tumor necrosis factor ; TOMM20: translocase of outer mitochondrial membrane 20; ULK1: unc-51 like kinase 1; VAMP8: vesicle-associated membrane protein 8; WT: wild type; 3-MA: 3-methyladenine</description><subject>ATP6V0D2</subject><subject>autophagosome-lysosome fusion</subject><subject>IL1B</subject><subject>inflammasome activation</subject><subject>Research Paper</subject><subject>Salmonella typhimurium</subject><issn>1554-8627</issn><issn>1554-8635</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kU2P0zAQhiMEYpeFnwDykUuKPxLHviBWy6e0EhzKXq2JY7dGTlxsZ1F_Cv8Wp-1WcOHkmfEz74zmraqXBK8IFvgNadtGcNqtKCZyRVouJeGPqsulXgvO2sfnmHYX1bOUfmDMuJD0aXXBMBeEyeay-r3eGjSCjmG3hY2p085oZ51Gd_X1-hskg9Lcz5PLqKT8Dr-nKJqUo9M5ITdZD-MIKYwGgc7uHrILE4JpQH3JTXTgF8roQ73fIwvaeZcLN20QzPkwNiwCtd-nQ4DsnAr9vHpiwSfz4vReVd8_fljffK5vv376cnN9W-uW41wDNqaxGBMmGqaZZbjHQlpBLSFSDqyh0Eg9GKmt5FLjzkDbG9JQiXHfdpRdVW-Puru5H82gzZQjeLWLboS4VwGc-vdnclu1CfeKt5QL2hWB1yeBGH7O5ThqdEkb72EyYU6Kkk42jeiELGh7RMu9U4rGnscQrBZb1YOtarFVnWwtfa_-3vHc9eBjAd4dgXLsEEf4FaIfVIa9D9FGmLRLiv1_xh9AebZF</recordid><startdate>20190603</startdate><enddate>20190603</enddate><creator>Xia, Yu</creator><creator>Liu, Na</creator><creator>Xie, Xiuxiu</creator><creator>Bi, Guoyu</creator><creator>Ba, Hongping</creator><creator>Li, Lin</creator><creator>Zhang, Jinxia</creator><creator>Deng, Xiaofei</creator><creator>Yao, Yao</creator><creator>Tang, Zhaohui</creator><creator>Yin, Binjiao</creator><creator>Wang, Jing</creator><creator>Jiang, Kan</creator><creator>Li, Zhuoya</creator><creator>Choi, Yongwon</creator><creator>Gong, Feili</creator><creator>Cheng, Xiang</creator><creator>O'Shea, John J</creator><creator>Chae, Jae Jin</creator><creator>Laurence, Arian</creator><creator>Yang, Xiang-Ping</creator><general>Taylor &amp; 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Although many key, widely expressed proteins that regulate autophagosome formation followed by lysosomal fusion have been identified, the possibilities of cell-specific elements that contribute to the autophagy fusion machinery have not been explored. Here we show that a macrophage-specific isoform of the vacuolar ATPase protein ATP6V0D2/subunit d2 is dispensable for lysosome acidification, but promotes the completion of autophagy via promotion of autophagosome-lysosome fusion through its interaction with STX17 and VAMP8. Atp6v0d2-deficient macrophages have augmented mitochondrial damage, enhanced inflammasome activation and reduced clearance of Salmonella typhimurium. The susceptibility of atp6v0d2 knockout mice to DSS-induced colitis and Salmonella typhimurium-induced death, highlights the in vivo significance of ATP6V0D2-mediated autophagosome-lysosome fusion. Together, our data identify ATP6V0D2 as a key component of macrophage-specific autophagosome-lysosome fusion machinery maintaining macrophage organelle homeostasis and, in turn, limiting both inflammation and bacterial infection. Abbreviations: ACTB/β-actin: actin, beta; ATG14: autophagy related 14; ATG16L1: autophagy related 16-like 1 (S. cerevisiae); ATP6V0D1/2: ATPase, H+ transporting, lysosomal V0 subunit D1/2; AIM2: absent in melanoma 2; BMDM: bone marrow-derived macrophage; CASP1: caspase 1; CGD: chronic granulomatous disease; CSF1/M-CSF: colony stimulating factor 1 (macrophage); CTSB: cathepsin B; DSS: dextran sodium sulfate; IL1B: interleukin 1 beta; IL6: interleukin 6; IRGM: immunity-related GTPase family M member; KO: knockout; LAMP1: lysosomal-associated membrane protein 1; LC3: microtubule-associated protein 1 light chain 3; LPS: lipo-polysaccaride; NLRP3: NLR family, pyrin domain containing 3; PYCARD/ASC: PYD and CARD domain containing; SNARE: soluble N-ethylmaleimide-sensitive factor attachment protein receptor; SNAP29: synaptosomal-associated protein 29; SQSTM1/p62: sequestosome 1; STX17: syntaxin 17; TLR: toll-like receptor; TNF: tumor necrosis factor ; TOMM20: translocase of outer mitochondrial membrane 20; ULK1: unc-51 like kinase 1; VAMP8: vesicle-associated membrane protein 8; WT: wild type; 3-MA: 3-methyladenine</abstract><cop>United States</cop><pub>Taylor &amp; Francis</pub><pmid>30681394</pmid><doi>10.1080/15548627.2019.1569916</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0003-0942-8292</orcidid><orcidid>https://orcid.org/0000-0001-9003-1772</orcidid><oa>free_for_read</oa></addata></record>
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subjects ATP6V0D2
autophagosome-lysosome fusion
IL1B
inflammasome activation
Research Paper
Salmonella typhimurium
title The macrophage-specific V-ATPase subunit ATP6V0D2 restricts inflammasome activation and bacterial infection by facilitating autophagosome-lysosome fusion
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