Biotechnological potential of Cannabis sativa adventitious roots for producing immunomodulatory and anti-inflammatory bioactive compounds

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dc.contributor.authorSu Hyun Park-
dc.contributor.authorJ M Han-
dc.contributor.authorYun Hye Kim-
dc.contributor.authorHyeon Jin Lee-
dc.contributor.authorYoung Bae Ryu-
dc.contributor.authorHyung Won Ryu-
dc.contributor.authorJae Cheol Jeong-
dc.contributor.authorSeon Min Oh-
dc.contributor.authorWoo Sik Kim-
dc.date.accessioned2025-08-25T16:32:31Z-
dc.date.available2025-08-25T16:32:31Z-
dc.date.issued2025-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/39333-
dc.description.abstractCannabis sativa L. (C. sativa), commonly known as hemp, is widely recognized for its diverse range of bioactive compounds with therapeutic potential in medicinal, industrial, and nutritional applications. This study investigates the use of adventitious roots (ARs) derived from C. sativa as a scalable platform for producing bioactive metabolites with immunomodulatory and anti-inflammatory properties. We first isolated extracts from C. sativa ARs (CS-AR) using various solvents: methanol (MeOH-E), chloroform (CHCl3-E), and hexane (Hexane-E), and explored their effects on dendritic cell (DC) maturation, a key process involved in immune responses. Notably, MeOH-E demonstrated strong anti-inflammatory effects without inducing cytotoxicity in DCs, distinguishing it from the other extracts. Metabolomic analysis of these extracts annotated the presence of cannabinoid derivatives and metabolites, including cannabinoid glycoside derivatives, cannabigerolic acid-O-acetate (CBGA-O-acetate), cannabidiol diacetate derivatives, and cannabidiol mono-acetate mono-benzoate. Among these, cannabinoid glycoside derivatives and CBGA-O-acetate were found to be present at higher levels in MeOH-E. Further investigation into the functional properties of MeOH-E revealed that it could suppress the expression of key surface molecules and antigen-presenting ability in mature DCs, alongside attenuating mitogen-activated protein kinase (MAPK) signaling pathways as well as nuclear factor kappa-B (NF-κB) signaling. Additionally, MeOH-E inhibited T cell proliferation and activation. These findings underscore the CS-AR system as a promising, reproducible biotechnological platform for producing therapeutic bioactive compounds for inflammatory diseases, with significant potential for application in the pharmaceutical and nutraceutical industries.-
dc.publisherSpringer-Nature Pub Group-
dc.titleBiotechnological potential of Cannabis sativa adventitious roots for producing immunomodulatory and anti-inflammatory bioactive compounds-
dc.title.alternativeBiotechnological potential of Cannabis sativa adventitious roots for producing immunomodulatory and anti-inflammatory bioactive compounds-
dc.typeArticle-
dc.citation.titleScientific Reports-
dc.citation.number0-
dc.citation.endPage30904-
dc.citation.startPage30904-
dc.citation.volume15-
dc.contributor.affiliatedAuthorSu Hyun Park-
dc.contributor.affiliatedAuthorYun Hye Kim-
dc.contributor.affiliatedAuthorHyeon Jin Lee-
dc.contributor.affiliatedAuthorYoung Bae Ryu-
dc.contributor.affiliatedAuthorHyung Won Ryu-
dc.contributor.affiliatedAuthorJae Cheol Jeong-
dc.contributor.affiliatedAuthorSeon Min Oh-
dc.contributor.affiliatedAuthorWoo Sik Kim-
dc.contributor.alternativeName박수현-
dc.contributor.alternativeName한정무-
dc.contributor.alternativeName김윤혜-
dc.contributor.alternativeName이현진-
dc.contributor.alternativeName류영배-
dc.contributor.alternativeName류형원-
dc.contributor.alternativeName정재철-
dc.contributor.alternativeName오선민-
dc.contributor.alternativeName김우식-
dc.identifier.bibliographicCitationScientific Reports, vol. 15, pp. 30904-30904-
dc.identifier.doi10.1038/s41598-025-16130-1-
dc.subject.keywordAdventitious roots-
dc.subject.keywordCannabis sativa L.,-
dc.subject.keywordDendritic cells-
dc.subject.keywordT cells-
dc.subject.keywordAnti-inflammatory activity-
dc.subject.keywordImmunosuppression-
dc.subject.localAdventitious roots-
dc.subject.localdendritic cell-
dc.subject.localdendritic cells-
dc.subject.localdendritic cells (DC)-
dc.subject.localDendritic cell-
dc.subject.localDendritic cells-
dc.subject.localDendritic cells (DC)-
dc.subject.localDendritic cells (DCs)-
dc.subject.localT cell-
dc.subject.localT cells-
dc.subject.localAnti-infl ammatory activity-
dc.subject.localAnti-inflammatory activity-
dc.subject.localanti-inflammatory activity-
dc.subject.localAnti-inflammatory activities-
dc.subject.localImmunosuppression-
dc.subject.localimmunosuppression-
dc.description.journalClassY-
Appears in Collections:
Jeonbuk Branch Institute > Functional Biomaterial Research Center > 1. Journal Articles
Ochang Branch Institute > Natural Product Research Center > 1. Journal Articles
Jeonbuk Branch Institute > Biological Resource Center > 1. Journal Articles
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