Intracellular acidification and glycolysis modulate inflammatory pathway in senescent cells
Senescent cells accumulate in various organs with ageing, and its accumulation induces chronic inflammation and age-related physiological dysfunctions. Several remodelling of intracellular environments have been identified in senescent cells, including enlargement of cell/nuclear size and intracellu...
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Veröffentlicht in: | Journal of biochemistry (Tokyo) 2024-07, Vol.176 (2), p.97-108 |
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creator | Kawakami, Satoshi Johmura, Yoshikazu Nakanishi, Makoto |
description | Senescent cells accumulate in various organs with ageing, and its accumulation induces chronic inflammation and age-related physiological dysfunctions. Several remodelling of intracellular environments have been identified in senescent cells, including enlargement of cell/nuclear size and intracellular acidification. Although these alterations of intracellular environments were reported to be involved in the unique characteristics of senescent cells, the contribution of intracellular acidification to senescence-associated cellular phenotypes is poorly understood. Here, we identified that the upregulation of TXNIP and its paralog ARRDC4 as a hallmark of intracellular acidification in addition to KGA-type GLS1. These genes were also upregulated in response to senescence-associated intracellular acidification. Neutralization of the intracellular acidic environment ameliorated not only senescence-related upregulation of TXNIP, ARRDC4 and KGA but also inflammation-related genes, possibly through suppression of PDK-dependent anaerobic glycolysis. Furthermore, we found that expression of the intracellular acidification-induced genes, TXNIP and ARRDC4, correlated with inflammatory gene expression in heterogeneous senescent cell population in vitro and even in vivo, implying that the contribution of intracellular pH to senescence-associated cellular features, such as SASP. |
doi_str_mv | 10.1093/jb/mvae032 |
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Several remodelling of intracellular environments have been identified in senescent cells, including enlargement of cell/nuclear size and intracellular acidification. Although these alterations of intracellular environments were reported to be involved in the unique characteristics of senescent cells, the contribution of intracellular acidification to senescence-associated cellular phenotypes is poorly understood. Here, we identified that the upregulation of TXNIP and its paralog ARRDC4 as a hallmark of intracellular acidification in addition to KGA-type GLS1. These genes were also upregulated in response to senescence-associated intracellular acidification. Neutralization of the intracellular acidic environment ameliorated not only senescence-related upregulation of TXNIP, ARRDC4 and KGA but also inflammation-related genes, possibly through suppression of PDK-dependent anaerobic glycolysis. Furthermore, we found that expression of the intracellular acidification-induced genes, TXNIP and ARRDC4, correlated with inflammatory gene expression in heterogeneous senescent cell population in vitro and even in vivo, implying that the contribution of intracellular pH to senescence-associated cellular features, such as SASP.</description><subject>Animals</subject><subject>Carrier Proteins - genetics</subject><subject>Carrier Proteins - metabolism</subject><subject>Cellular Senescence</subject><subject>Glycolysis</subject><subject>Humans</subject><subject>Hydrogen-Ion Concentration</subject><subject>Inflammation - metabolism</subject><subject>Inflammation - pathology</subject><subject>Mice</subject><subject>Regular Paper</subject><issn>0021-924X</issn><issn>1756-2651</issn><issn>1756-2651</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkV1LwzAUhoMobk5v_AHSSxHq8tEk7ZXI8AsG3igIXoSzNN0y2mYm7aT_3pbNoVcnJ3l4857zInRJ8C3BGZuuF9NqCwYzeoTGRHIRU8HJMRpjTEmc0eRjhM5CWA8tZewUjVjKRUKpHKPPl7rxoE1ZtiX4CLTNbWE1NNbVEdR5tCw77cou2BBVLu-hxkS2LkqoKmic76INNKtv6PrLKJjaBG3qJhoEwzk6KaAM5mJfJ-j98eFt9hzPX59eZvfzWNOMN3HKU2BFyjKmC1xwJrSkaSIJYUwLAjKTUlCMuZAyE2lOhMhB90csFxngJGETdLfT3bSLyuSDAQ-l2nhbge-UA6v-v9R2pZZuqwihacYo7hWu9wrefbUmNKqyYZgBauPaoBhmgx2eyB692aHauxC8KQ7_EKyGONR6ofZx9PDVX2cH9Hf_7AdO0YhJ</recordid><startdate>20240731</startdate><enddate>20240731</enddate><creator>Kawakami, Satoshi</creator><creator>Johmura, Yoshikazu</creator><creator>Nakanishi, Makoto</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20240731</creationdate><title>Intracellular acidification and glycolysis modulate inflammatory pathway in senescent cells</title><author>Kawakami, Satoshi ; Johmura, Yoshikazu ; Nakanishi, Makoto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c295t-858a3f8393cf0f536c728471133c61a797762005677968d166dac79607b9a0443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Carrier Proteins - genetics</topic><topic>Carrier Proteins - metabolism</topic><topic>Cellular Senescence</topic><topic>Glycolysis</topic><topic>Humans</topic><topic>Hydrogen-Ion Concentration</topic><topic>Inflammation - metabolism</topic><topic>Inflammation - pathology</topic><topic>Mice</topic><topic>Regular Paper</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kawakami, Satoshi</creatorcontrib><creatorcontrib>Johmura, Yoshikazu</creatorcontrib><creatorcontrib>Nakanishi, Makoto</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of biochemistry (Tokyo)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kawakami, Satoshi</au><au>Johmura, Yoshikazu</au><au>Nakanishi, Makoto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intracellular acidification and glycolysis modulate inflammatory pathway in senescent cells</atitle><jtitle>Journal of biochemistry (Tokyo)</jtitle><addtitle>J Biochem</addtitle><date>2024-07-31</date><risdate>2024</risdate><volume>176</volume><issue>2</issue><spage>97</spage><epage>108</epage><pages>97-108</pages><issn>0021-924X</issn><issn>1756-2651</issn><eissn>1756-2651</eissn><abstract>Senescent cells accumulate in various organs with ageing, and its accumulation induces chronic inflammation and age-related physiological dysfunctions. Several remodelling of intracellular environments have been identified in senescent cells, including enlargement of cell/nuclear size and intracellular acidification. Although these alterations of intracellular environments were reported to be involved in the unique characteristics of senescent cells, the contribution of intracellular acidification to senescence-associated cellular phenotypes is poorly understood. Here, we identified that the upregulation of TXNIP and its paralog ARRDC4 as a hallmark of intracellular acidification in addition to KGA-type GLS1. These genes were also upregulated in response to senescence-associated intracellular acidification. Neutralization of the intracellular acidic environment ameliorated not only senescence-related upregulation of TXNIP, ARRDC4 and KGA but also inflammation-related genes, possibly through suppression of PDK-dependent anaerobic glycolysis. Furthermore, we found that expression of the intracellular acidification-induced genes, TXNIP and ARRDC4, correlated with inflammatory gene expression in heterogeneous senescent cell population in vitro and even in vivo, implying that the contribution of intracellular pH to senescence-associated cellular features, such as SASP.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>38564227</pmid><doi>10.1093/jb/mvae032</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Oxford University Press Journals All Titles (1996-Current) |
subjects | Animals Carrier Proteins - genetics Carrier Proteins - metabolism Cellular Senescence Glycolysis Humans Hydrogen-Ion Concentration Inflammation - metabolism Inflammation - pathology Mice Regular Paper |
title | Intracellular acidification and glycolysis modulate inflammatory pathway in senescent cells |
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