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3,4-Dihydroxybenzalacetone Inhibits the Propagation of Hydrogen Peroxide-Induced Oxidative Effect via Secretory Components from SH-SY5Y Cells
The polyphenol derivative 3,4-dihydroxybenzalacetone (DBL) is the primary antioxidative component of the medicinal folk mushroom Chaga (Inonotus obliquus (persoon) Pilat). In this study, we investigated whether the antioxidative effect of DBL could propagate to recipient cells via secreted component...
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Published in: | Biological & pharmaceutical bulletin 2023-04, Vol.46 (4), p.599-607, Article b22-00727 |
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creator | Ikemoto, Mitsushi J Aihara, Yukine Ishii, Noriyuki Shigemori, Hideyuki |
description | The polyphenol derivative 3,4-dihydroxybenzalacetone (DBL) is the primary antioxidative component of the medicinal folk mushroom Chaga (Inonotus obliquus (persoon) Pilat). In this study, we investigated whether the antioxidative effect of DBL could propagate to recipient cells via secreted components, including extracellular vesicles (EVs), after pre-exposing SH-SY5Y human neuroblastoma cells to DBL. First, we prepared EV-enriched fractions via sucrose density gradient ultracentrifugation using conditioned medium from SH-SY5Y cells exposed to 100 µM hydrogen peroxide (H
O
) for 24 h, with and without 1 h of 5 µM DBL pre-treatment. CD63 immuno-dot blot analysis demonstrated that fractions with density of 1.06-1.09 g/cm
had CD63-like immuno-reactivities. Furthermore, the 2,2-diphenyl-1-picrylhydrazyl assay revealed that the radical scavenging activity of fraction 11 (density of 1.06 g/cm
), prepared after 24-h H
O
treatment, was significantly increased compared to that in the control group (no H
O
treatment). Notably, 1 h of 5 µM DBL pre-treatment or 5 min of heat treatment (100 °C) diminished this effect, although concentrating the fraction by 100 kDa ultrafiltration enhanced it. Overall, the effect was not specific to the recipient cell types. In addition, the uptake of fluorescent Paul Karl Horan-labeled EVs in concentrated fraction 11 was detected in all treatment groups, particularly in the H
O
-treated group. The results suggest that cell-to-cell communication via bioactive substances, such as EVs, in conditioned SH-SY5Y cell medium, propagates the H
O
-induced radical scavenging effect, whereas pre-conditioning with DBL inhibits it. |
doi_str_mv | 10.1248/bpb.b22-00727 |
format | article |
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O
) for 24 h, with and without 1 h of 5 µM DBL pre-treatment. CD63 immuno-dot blot analysis demonstrated that fractions with density of 1.06-1.09 g/cm
had CD63-like immuno-reactivities. Furthermore, the 2,2-diphenyl-1-picrylhydrazyl assay revealed that the radical scavenging activity of fraction 11 (density of 1.06 g/cm
), prepared after 24-h H
O
treatment, was significantly increased compared to that in the control group (no H
O
treatment). Notably, 1 h of 5 µM DBL pre-treatment or 5 min of heat treatment (100 °C) diminished this effect, although concentrating the fraction by 100 kDa ultrafiltration enhanced it. Overall, the effect was not specific to the recipient cell types. In addition, the uptake of fluorescent Paul Karl Horan-labeled EVs in concentrated fraction 11 was detected in all treatment groups, particularly in the H
O
-treated group. The results suggest that cell-to-cell communication via bioactive substances, such as EVs, in conditioned SH-SY5Y cell medium, propagates the H
O
-induced radical scavenging effect, whereas pre-conditioning with DBL inhibits it.</description><identifier>ISSN: 0918-6158</identifier><identifier>EISSN: 1347-5215</identifier><identifier>DOI: 10.1248/bpb.b22-00727</identifier><identifier>PMID: 37005304</identifier><language>eng</language><publisher>Japan: Japan Science and Technology Agency</publisher><subject>Antioxidants - pharmacology ; Apoptosis ; CD63 antigen ; Cell interactions ; Cell Line, Tumor ; Cell Survival ; Heat treatments ; Humans ; Hydrogen peroxide ; Hydrogen Peroxide - pharmacology ; Neuroblastoma ; Neuroblastoma cells ; Oxidative Stress ; Secretory Component - pharmacology ; Ultracentrifugation ; Ultrafiltration</subject><ispartof>Biological & pharmaceutical bulletin, 2023-04, Vol.46 (4), p.599-607, Article b22-00727</ispartof><rights>Copyright Japan Science and Technology Agency 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c463t-48a328b1457808af43a4b302a698715cf0363dcb8efa638d062be5e23c9393303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37005304$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ikemoto, Mitsushi J</creatorcontrib><creatorcontrib>Aihara, Yukine</creatorcontrib><creatorcontrib>Ishii, Noriyuki</creatorcontrib><creatorcontrib>Shigemori, Hideyuki</creatorcontrib><title>3,4-Dihydroxybenzalacetone Inhibits the Propagation of Hydrogen Peroxide-Induced Oxidative Effect via Secretory Components from SH-SY5Y Cells</title><title>Biological & pharmaceutical bulletin</title><addtitle>Biol Pharm Bull</addtitle><description>The polyphenol derivative 3,4-dihydroxybenzalacetone (DBL) is the primary antioxidative component of the medicinal folk mushroom Chaga (Inonotus obliquus (persoon) Pilat). In this study, we investigated whether the antioxidative effect of DBL could propagate to recipient cells via secreted components, including extracellular vesicles (EVs), after pre-exposing SH-SY5Y human neuroblastoma cells to DBL. First, we prepared EV-enriched fractions via sucrose density gradient ultracentrifugation using conditioned medium from SH-SY5Y cells exposed to 100 µM hydrogen peroxide (H
O
) for 24 h, with and without 1 h of 5 µM DBL pre-treatment. CD63 immuno-dot blot analysis demonstrated that fractions with density of 1.06-1.09 g/cm
had CD63-like immuno-reactivities. Furthermore, the 2,2-diphenyl-1-picrylhydrazyl assay revealed that the radical scavenging activity of fraction 11 (density of 1.06 g/cm
), prepared after 24-h H
O
treatment, was significantly increased compared to that in the control group (no H
O
treatment). Notably, 1 h of 5 µM DBL pre-treatment or 5 min of heat treatment (100 °C) diminished this effect, although concentrating the fraction by 100 kDa ultrafiltration enhanced it. Overall, the effect was not specific to the recipient cell types. In addition, the uptake of fluorescent Paul Karl Horan-labeled EVs in concentrated fraction 11 was detected in all treatment groups, particularly in the H
O
-treated group. The results suggest that cell-to-cell communication via bioactive substances, such as EVs, in conditioned SH-SY5Y cell medium, propagates the H
O
-induced radical scavenging effect, whereas pre-conditioning with DBL inhibits it.</description><subject>Antioxidants - pharmacology</subject><subject>Apoptosis</subject><subject>CD63 antigen</subject><subject>Cell interactions</subject><subject>Cell Line, Tumor</subject><subject>Cell Survival</subject><subject>Heat treatments</subject><subject>Humans</subject><subject>Hydrogen peroxide</subject><subject>Hydrogen Peroxide - pharmacology</subject><subject>Neuroblastoma</subject><subject>Neuroblastoma cells</subject><subject>Oxidative Stress</subject><subject>Secretory Component - pharmacology</subject><subject>Ultracentrifugation</subject><subject>Ultrafiltration</subject><issn>0918-6158</issn><issn>1347-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkc9rFDEUgIModq0evUrAiwdT83syR1mru1BoYfXQU0gyb7pTdpIxmSmu_4P_s6mtHjw9Hnzv48GH0GtGzxiX5oOf_JnnnFDa8OYJWjEhG6I4U0_RirbMEM2UOUEvSrmllaFcPEcnoqFUCSpX6Jd4L8mnYX_scvpx9BB_uoMLMKcIeBv3gx_mguc94KucJnfj5iFFnHq8uT-4gYivoB4OHZBt7JYAHb6sW8XuAJ_3PYQZ3w0O7yDkKs1HvE7jVOWxavucRrzbkN21usZrOBzKS_Ssd4cCrx7nKfr2-fzrekMuLr9s1x8vSJBazEQaJ7jxTKrGUON6KZz0gnKnW9MwFXoqtOiCN9A7LUxHNfeggIvQilYIKk7RuwfvlNP3Bcpsx6GE-oGLkJZiedNKbTTTsqJv_0Nv05Jj_c5yw1XTti01lSIPVMiplAy9nfIwuny0jNr7TrZ2srWT_dOp8m8erYsfoftH_w0jfgOUz45X</recordid><startdate>20230401</startdate><enddate>20230401</enddate><creator>Ikemoto, Mitsushi J</creator><creator>Aihara, Yukine</creator><creator>Ishii, Noriyuki</creator><creator>Shigemori, Hideyuki</creator><general>Japan Science and Technology Agency</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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20230401</creationdate><title>3,4-Dihydroxybenzalacetone Inhibits the Propagation of Hydrogen Peroxide-Induced Oxidative Effect via Secretory Components from SH-SY5Y Cells</title><author>Ikemoto, Mitsushi J ; Aihara, Yukine ; Ishii, Noriyuki ; Shigemori, Hideyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-48a328b1457808af43a4b302a698715cf0363dcb8efa638d062be5e23c9393303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antioxidants - pharmacology</topic><topic>Apoptosis</topic><topic>CD63 antigen</topic><topic>Cell interactions</topic><topic>Cell Line, Tumor</topic><topic>Cell Survival</topic><topic>Heat treatments</topic><topic>Humans</topic><topic>Hydrogen peroxide</topic><topic>Hydrogen Peroxide - pharmacology</topic><topic>Neuroblastoma</topic><topic>Neuroblastoma cells</topic><topic>Oxidative Stress</topic><topic>Secretory Component - pharmacology</topic><topic>Ultracentrifugation</topic><topic>Ultrafiltration</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ikemoto, Mitsushi J</creatorcontrib><creatorcontrib>Aihara, Yukine</creatorcontrib><creatorcontrib>Ishii, Noriyuki</creatorcontrib><creatorcontrib>Shigemori, Hideyuki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biological & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ikemoto, Mitsushi J</au><au>Aihara, Yukine</au><au>Ishii, Noriyuki</au><au>Shigemori, Hideyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>3,4-Dihydroxybenzalacetone Inhibits the Propagation of Hydrogen Peroxide-Induced Oxidative Effect via Secretory Components from SH-SY5Y Cells</atitle><jtitle>Biological & pharmaceutical bulletin</jtitle><addtitle>Biol Pharm Bull</addtitle><date>2023-04-01</date><risdate>2023</risdate><volume>46</volume><issue>4</issue><spage>599</spage><epage>607</epage><pages>599-607</pages><artnum>b22-00727</artnum><issn>0918-6158</issn><eissn>1347-5215</eissn><abstract>The polyphenol derivative 3,4-dihydroxybenzalacetone (DBL) is the primary antioxidative component of the medicinal folk mushroom Chaga (Inonotus obliquus (persoon) Pilat). In this study, we investigated whether the antioxidative effect of DBL could propagate to recipient cells via secreted components, including extracellular vesicles (EVs), after pre-exposing SH-SY5Y human neuroblastoma cells to DBL. First, we prepared EV-enriched fractions via sucrose density gradient ultracentrifugation using conditioned medium from SH-SY5Y cells exposed to 100 µM hydrogen peroxide (H
O
) for 24 h, with and without 1 h of 5 µM DBL pre-treatment. CD63 immuno-dot blot analysis demonstrated that fractions with density of 1.06-1.09 g/cm
had CD63-like immuno-reactivities. Furthermore, the 2,2-diphenyl-1-picrylhydrazyl assay revealed that the radical scavenging activity of fraction 11 (density of 1.06 g/cm
), prepared after 24-h H
O
treatment, was significantly increased compared to that in the control group (no H
O
treatment). Notably, 1 h of 5 µM DBL pre-treatment or 5 min of heat treatment (100 °C) diminished this effect, although concentrating the fraction by 100 kDa ultrafiltration enhanced it. Overall, the effect was not specific to the recipient cell types. In addition, the uptake of fluorescent Paul Karl Horan-labeled EVs in concentrated fraction 11 was detected in all treatment groups, particularly in the H
O
-treated group. The results suggest that cell-to-cell communication via bioactive substances, such as EVs, in conditioned SH-SY5Y cell medium, propagates the H
O
-induced radical scavenging effect, whereas pre-conditioning with DBL inhibits it.</abstract><cop>Japan</cop><pub>Japan Science and Technology Agency</pub><pmid>37005304</pmid><doi>10.1248/bpb.b22-00727</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antioxidants - pharmacology Apoptosis CD63 antigen Cell interactions Cell Line, Tumor Cell Survival Heat treatments Humans Hydrogen peroxide Hydrogen Peroxide - pharmacology Neuroblastoma Neuroblastoma cells Oxidative Stress Secretory Component - pharmacology Ultracentrifugation Ultrafiltration |
title | 3,4-Dihydroxybenzalacetone Inhibits the Propagation of Hydrogen Peroxide-Induced Oxidative Effect via Secretory Components from SH-SY5Y Cells |
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