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Self-assembled hyaluronic acid nanoparticle suppresses fat accumulation via CD44 in diet-induced obese mice
  • Lee, Wang Hee ;
  • Rho, Jun Gi ;
  • Han, Hwa Seung ;
  • Kweon, Sohui ;
  • Nguyen, Van Quy ;
  • Park, Jae Hyung ;
  • Kim, Wook
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dc.contributor.authorLee, Wang Hee-
dc.contributor.authorRho, Jun Gi-
dc.contributor.authorHan, Hwa Seung-
dc.contributor.authorKweon, Sohui-
dc.contributor.authorNguyen, Van Quy-
dc.contributor.authorPark, Jae Hyung-
dc.contributor.authorKim, Wook-
dc.date.issued2020-06-01-
dc.identifier.issn0144-8617-
dc.identifier.urihttps://dspace.ajou.ac.kr/dev/handle/2018.oak/31207-
dc.description.abstractObesity, a major risk factor for type 2 diabetes and cardiovascular diseases, is characterized by an abnormal expansion of adipose tissue. Herein, we investigated the potential of hyaluronic acid nanoparticles (HA-NPs) as therapeutics to treat obesity-related diseases by assessing the in vitro and in vivo effects of HA-NPs on adipogenesis and lipogenesis. Treatment of 3T3-L1 preadipocytes with HA-NPs resulted in a dose-dependent suppression of adipogenesis and lipid accumulation, and decreased the expression of key adipogenic and lipogenic regulators. However, these HA-NPs mediated effects were not observed in 3T3-L1 cells transfected with siRNAs against CD44, a major HA receptor. Further, HA-NP treatment of diet-induced obese (DIO) mice reduced the epididymal fat mass and suppressed the induction of adipogenic and lipogenic regulators, while these effects were attenuated in the CD44-null mice. Thus, our study provides a better understanding of how HA-NP modulates fat accumulation and presents a potential anti-obesity strategy targeting CD44.-
dc.description.sponsorshipThis work was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education ( 2019R1A6A1A11051471 ) and the Ministry of Science and ICT ( 2016R1E1A1A01941213 , 2019R1A2B5B03100464 , 2019M3E5D5066525 ).-
dc.language.isoeng-
dc.publisherElsevier Ltd-
dc.subject.mesh3t3-l1 preadipocytes-
dc.subject.meshAbnormal expansion-
dc.subject.meshAdipogenesis-
dc.subject.meshCardio-vascular disease-
dc.subject.meshLipid accumulations-
dc.subject.meshLipogenesis-
dc.subject.meshObesity-
dc.subject.meshSelf assembled nanoparticles-
dc.subject.mesh3T3-L1 Cells-
dc.subject.meshAdipogenesis-
dc.subject.meshAnimals-
dc.subject.meshDiet, High-Fat-
dc.subject.meshHyaluronan Receptors-
dc.subject.meshHyaluronic Acid-
dc.subject.meshLipogenesis-
dc.subject.meshMale-
dc.subject.meshMice-
dc.subject.meshMice, Inbred C57BL-
dc.subject.meshMice, Knockout-
dc.subject.meshNanoparticles-
dc.subject.meshObesity-
dc.titleSelf-assembled hyaluronic acid nanoparticle suppresses fat accumulation via CD44 in diet-induced obese mice-
dc.typeArticle-
dc.citation.titleCarbohydrate Polymers-
dc.citation.volume237-
dc.identifier.bibliographicCitationCarbohydrate Polymers, Vol.237-
dc.identifier.doi10.1016/j.carbpol.2020.116161-
dc.identifier.pmid32241446-
dc.identifier.scopusid2-s2.0-85081647120-
dc.identifier.urlhttp://www.elsevier.com/wps/find/journaldescription.cws_home/405871/description#description-
dc.subject.keywordAdipogenesis-
dc.subject.keywordHyaluronic acid-
dc.subject.keywordLipogenesis-
dc.subject.keywordObesity-
dc.subject.keywordSelf-assembled nanoparticles-
dc.description.isoafalse-
dc.subject.subareaOrganic Chemistry-
dc.subject.subareaPolymers and Plastics-
dc.subject.subareaMaterials Chemistry-
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