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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
Citations

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Publication Year
2020-06-01
Publisher
Elsevier Ltd
Citation
Carbohydrate Polymers, Vol.237
Keyword
AdipogenesisHyaluronic acidLipogenesisObesitySelf-assembled nanoparticles
Mesh Keyword
3t3-l1 preadipocytesAbnormal expansionAdipogenesisCardio-vascular diseaseLipid accumulationsLipogenesisObesitySelf assembled nanoparticles3T3-L1 CellsAdipogenesisAnimalsDiet, High-FatHyaluronan ReceptorsHyaluronic AcidLipogenesisMaleMiceMice, Inbred C57BLMice, KnockoutNanoparticlesObesity
All Science Classification Codes (ASJC)
Organic ChemistryPolymers and PlasticsMaterials Chemistry
Abstract
Obesity, 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.
ISSN
0144-8617
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/31207
DOI
https://doi.org/10.1016/j.carbpol.2020.116161
Fulltext

Type
Article
Funding
This 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 ).
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College of Bio-convergence Engineering
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