Host-commensal interaction promotes health and lifespan in Caenorhabditis elegans through the activation of HLH-30/TFEB-mediated autophagy
Gut homeostasis is maintained by the close interaction between commensal intestinal microbiota and the host, affecting the most complex physiological processes, such as aging. Some commensal bacteria with the potential to promote healthy aging arise as attractive candidates for the development of pr...
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Veröffentlicht in: | Aging (Albany, NY.) NY.), 2021-03, Vol.13 (6), p.8040-8054 |
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creator | Dinić, Miroslav Herholz, Marija Kačarević, Uroš Radojević, Dušan Novović, Katarina Đokić, Jelena Trifunović, Aleksandra Golić, Nataša |
description | Gut homeostasis is maintained by the close interaction between commensal intestinal microbiota and the host, affecting the most complex physiological processes, such as aging. Some commensal bacteria with the potential to promote healthy aging arise as attractive candidates for the development of pro-longevity probiotics. Here, we showed that heat-inactivated human commensal
BGHV110 (BGHV110) extends the lifespan of
and improves age-related physiological features, including locomotor function and lipid metabolism. Mechanistically, we found that BGHV110 promotes HLH-30/TFEB-dependent autophagy to delay aging, as longevity assurance was completely abolished in the mutant lacking HLH-30, a major autophagy regulator in
. Moreover, we observed that BGHV110 partially decreased the content of lipid droplets in an HLH-30-dependent manner and, at the same time, slightly increased mitochondrial activity. In summary, this study demonstrates that specific factors from commensal bacteria can be used to exploit HLH-30/TFEB-mediated autophagy in order to promote longevity and fitness of the host. |
doi_str_mv | 10.18632/aging.202885 |
format | Article |
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BGHV110 (BGHV110) extends the lifespan of
and improves age-related physiological features, including locomotor function and lipid metabolism. Mechanistically, we found that BGHV110 promotes HLH-30/TFEB-dependent autophagy to delay aging, as longevity assurance was completely abolished in the mutant lacking HLH-30, a major autophagy regulator in
. Moreover, we observed that BGHV110 partially decreased the content of lipid droplets in an HLH-30-dependent manner and, at the same time, slightly increased mitochondrial activity. In summary, this study demonstrates that specific factors from commensal bacteria can be used to exploit HLH-30/TFEB-mediated autophagy in order to promote longevity and fitness of the host.</description><identifier>ISSN: 1945-4589</identifier><identifier>EISSN: 1945-4589</identifier><identifier>DOI: 10.18632/aging.202885</identifier><identifier>PMID: 33770762</identifier><language>eng</language><publisher>United States: Impact Journals</publisher><subject>Research Paper</subject><ispartof>Aging (Albany, NY.), 2021-03, Vol.13 (6), p.8040-8054</ispartof><rights>Copyright: © 2021 Dinić et al.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-f86716cde9822331db8bd5df43f2f21e65712d5e8ef49fb7c1a34b1a0a3258d73</citedby><cites>FETCH-LOGICAL-c387t-f86716cde9822331db8bd5df43f2f21e65712d5e8ef49fb7c1a34b1a0a3258d73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8034897/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8034897/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33770762$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dinić, Miroslav</creatorcontrib><creatorcontrib>Herholz, Marija</creatorcontrib><creatorcontrib>Kačarević, Uroš</creatorcontrib><creatorcontrib>Radojević, Dušan</creatorcontrib><creatorcontrib>Novović, Katarina</creatorcontrib><creatorcontrib>Đokić, Jelena</creatorcontrib><creatorcontrib>Trifunović, Aleksandra</creatorcontrib><creatorcontrib>Golić, Nataša</creatorcontrib><title>Host-commensal interaction promotes health and lifespan in Caenorhabditis elegans through the activation of HLH-30/TFEB-mediated autophagy</title><title>Aging (Albany, NY.)</title><addtitle>Aging (Albany NY)</addtitle><description>Gut homeostasis is maintained by the close interaction between commensal intestinal microbiota and the host, affecting the most complex physiological processes, such as aging. Some commensal bacteria with the potential to promote healthy aging arise as attractive candidates for the development of pro-longevity probiotics. Here, we showed that heat-inactivated human commensal
BGHV110 (BGHV110) extends the lifespan of
and improves age-related physiological features, including locomotor function and lipid metabolism. Mechanistically, we found that BGHV110 promotes HLH-30/TFEB-dependent autophagy to delay aging, as longevity assurance was completely abolished in the mutant lacking HLH-30, a major autophagy regulator in
. Moreover, we observed that BGHV110 partially decreased the content of lipid droplets in an HLH-30-dependent manner and, at the same time, slightly increased mitochondrial activity. In summary, this study demonstrates that specific factors from commensal bacteria can be used to exploit HLH-30/TFEB-mediated autophagy in order to promote longevity and fitness of the host.</description><subject>Research Paper</subject><issn>1945-4589</issn><issn>1945-4589</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpVkU1v1DAQhiMEoqVw5Ip85JLWH3HiXJBg1bJIK3EpZ2sSjxOjxA62U6l_ob-adLdU5fSONI-eGektio-MXjJVC34Fg_PDJadcKfmqOGdtJctKqvb1i_mseJfSb0prKav6bXEmRNPQpubnxcM-pFz2YZ7RJ5iI8xkj9NkFT5YY5pAxkRFhyiMBb8jkLKYF_AaSHaAPcYTOuOwSwQkH8InkMYZ1GLdE8mi6g6MtWLI_7EtBr25vrr-VMxoHGQ2BNYdlhOH-ffHGwpTww1NeFL9urm93-_Lw8_uP3ddD2QvV5NKqumF1b7BVnAvBTKc6I42thOWWM6xlw7iRqNBWre2anoGoOgYUBJfKNOKi-HLyLmu3fdGjzxEmvUQ3Q7zXAZz-f-PdqIdwpxUVlWofBZ-fBDH8WTFlPbvU4zSBx7AmzSWtecsElRtantA-hpQi2uczjOpjf_rYnz71t_GfXv72TP8rTPwFcVCazg</recordid><startdate>20210326</startdate><enddate>20210326</enddate><creator>Dinić, Miroslav</creator><creator>Herholz, Marija</creator><creator>Kačarević, Uroš</creator><creator>Radojević, Dušan</creator><creator>Novović, Katarina</creator><creator>Đokić, Jelena</creator><creator>Trifunović, Aleksandra</creator><creator>Golić, Nataša</creator><general>Impact Journals</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210326</creationdate><title>Host-commensal interaction promotes health and lifespan in Caenorhabditis elegans through the activation of HLH-30/TFEB-mediated autophagy</title><author>Dinić, Miroslav ; Herholz, Marija ; Kačarević, Uroš ; Radojević, Dušan ; Novović, Katarina ; Đokić, Jelena ; Trifunović, Aleksandra ; Golić, Nataša</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-f86716cde9822331db8bd5df43f2f21e65712d5e8ef49fb7c1a34b1a0a3258d73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Research Paper</topic><toplevel>online_resources</toplevel><creatorcontrib>Dinić, Miroslav</creatorcontrib><creatorcontrib>Herholz, Marija</creatorcontrib><creatorcontrib>Kačarević, Uroš</creatorcontrib><creatorcontrib>Radojević, Dušan</creatorcontrib><creatorcontrib>Novović, Katarina</creatorcontrib><creatorcontrib>Đokić, Jelena</creatorcontrib><creatorcontrib>Trifunović, Aleksandra</creatorcontrib><creatorcontrib>Golić, Nataša</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Aging (Albany, NY.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dinić, Miroslav</au><au>Herholz, Marija</au><au>Kačarević, Uroš</au><au>Radojević, Dušan</au><au>Novović, Katarina</au><au>Đokić, Jelena</au><au>Trifunović, Aleksandra</au><au>Golić, Nataša</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Host-commensal interaction promotes health and lifespan in Caenorhabditis elegans through the activation of HLH-30/TFEB-mediated autophagy</atitle><jtitle>Aging (Albany, NY.)</jtitle><addtitle>Aging (Albany NY)</addtitle><date>2021-03-26</date><risdate>2021</risdate><volume>13</volume><issue>6</issue><spage>8040</spage><epage>8054</epage><pages>8040-8054</pages><issn>1945-4589</issn><eissn>1945-4589</eissn><abstract>Gut homeostasis is maintained by the close interaction between commensal intestinal microbiota and the host, affecting the most complex physiological processes, such as aging. Some commensal bacteria with the potential to promote healthy aging arise as attractive candidates for the development of pro-longevity probiotics. Here, we showed that heat-inactivated human commensal
BGHV110 (BGHV110) extends the lifespan of
and improves age-related physiological features, including locomotor function and lipid metabolism. Mechanistically, we found that BGHV110 promotes HLH-30/TFEB-dependent autophagy to delay aging, as longevity assurance was completely abolished in the mutant lacking HLH-30, a major autophagy regulator in
. Moreover, we observed that BGHV110 partially decreased the content of lipid droplets in an HLH-30-dependent manner and, at the same time, slightly increased mitochondrial activity. In summary, this study demonstrates that specific factors from commensal bacteria can be used to exploit HLH-30/TFEB-mediated autophagy in order to promote longevity and fitness of the host.</abstract><cop>United States</cop><pub>Impact Journals</pub><pmid>33770762</pmid><doi>10.18632/aging.202885</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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title | Host-commensal interaction promotes health and lifespan in Caenorhabditis elegans through the activation of HLH-30/TFEB-mediated autophagy |
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