NRF2 activation by 2-methoxycinnamaldehyde attenuates inflammatory responses in macrophages via enhancing autophagy flux

被引:3
作者
Kim, Bo-Sung [1 ,2 ]
Shin, Minwook [3 ]
Kim, Kyu-Won [4 ,5 ]
Ha, Ki-Tae [1 ,2 ]
Bae, Sung-Jin [6 ]
机构
[1] Pusan Natl Univ, Sch Korean Med, Dept Korean Med Sci, Yangsan 50612, South Korea
[2] Pusan Natl Univ, Korean Med Res Ctr Hlth Aging, Yangsan 50612, South Korea
[3] Univ Massachusetts, RNA Therapeut Inst, Chan Med Sch, Worcester, MA 01605 USA
[4] Seoul Natl Univ, Coll Pharm, Seoul 08826, South Korea
[5] Seoul Natl Univ, Res Inst Pharmaceut Sci, Seoul 08826, South Korea
[6] Kosin Univ, Dept Mol Biol & Immunol, Coll Med, Busan 49267, South Korea
基金
新加坡国家研究基金会;
关键词
2-Methoxycinnamaldehyde; Autophagy; Inflammation; LPS; NRF2; NITRIC-OXIDE; OXIDATIVE STRESS; KAPPA-B; P62/SQSTM1; PROTECTS;
D O I
10.5483/BMBRep.2022.55.8.065
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A well-controlled inflammatory response is crucial for the recovery from injury and maintenance of tissue homeostasis. The anti-inflammatory response of 2-methoxycinnamaldehyde (2-MCA), a natural compound derived from cinnamon, has been studied; however, the underlying mechanism on macrophage has not been fully elucidated. In this study, LPS-stimulated production of TNF-alpha and NO was reduced by 2-MCA in macrophages. 2-MCA significantly activated the NRF2 pathway, and expression levels of autophagy-associated proteins in macrophages, including LC3 and P62, were enhanced via NRF2 activation regard-less of LPS treatment, suggesting the occurrence of 2-MCA -mediated autophagy. Moreover, evaluation of autophagy flux using luciferase-conjugated LC3 revealed that incremental LC3 and P62 levels are coupled to enhanced autophagy flux. Finally, reduced expression levels of TNF-alpha and NOS2 by 2-MCA were reversed by autophagy inhibitors, such as bafilomycin A1 and NH4Cl, in LPS-stimulated macrophages. In conclusion, 2-MCA enhances autophagy flux in macrophages via NRF2 activation and consequently reduces LPS-induced inflammation.
引用
收藏
页码:407 / 412
页数:6
相关论文
共 36 条
[1]   The Molecular Mechanisms Regulating the KEAP1-NRF2 Pathway [J].
Baird, Liam ;
Yamamoto, Masayuki .
MOLECULAR AND CELLULAR BIOLOGY, 2020, 40 (13)
[2]   Nrf2-Keap1 signaling in oxidative and reductive stress [J].
Bellezza, Ilaria ;
Giambanco, Ileana ;
Minelli, Alba ;
Donato, Rosario .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2018, 1865 (05) :721-733
[3]   Hyper-inflammatory responses in COVID-19 and anti-inflammatory therapeutic approaches [J].
Choi, Hojun ;
Shin, Eui-Cheol .
BMB REPORTS, 2022, 55 (01) :11-19
[4]   Cytokine storm and sepsis disease pathogenesis [J].
Chousterman, Benjamin G. ;
Swirski, Filip K. ;
Weber, Georg F. .
SEMINARS IN IMMUNOPATHOLOGY, 2017, 39 (05) :517-528
[5]   Renilla Luciferase-LC3 Based Reporter Assay for Measuring Autophagic Flux [J].
Farkas, T. ;
Jaattela, M. .
MOLECULAR CHARACTERIZATION OF AUTOPHAGIC RESPONSES, PT B, 2017, 588 :1-13
[6]   The protective role of autophagy in sepsis [J].
Feng, Ying ;
Liu, Boyi ;
Zheng, Xiang ;
Chen, Li ;
Chen, Wei ;
Fang, Zhicheng .
MICROBIAL PATHOGENESIS, 2019, 131 :106-111
[7]   Nrf2 positively regulates autophagy antioxidant response in human bronchial epithelial cells exposed to diesel exhaust particles [J].
Frias, Daniela Perroni ;
Nunes Gomes, Raquel Labiapari ;
Yoshizaki, Kelly ;
Carvalho-Oliveira, Regiani ;
Matsuda, Monique ;
Junqueira, Mara de Souza ;
Teodoro, Walcy Rosolia ;
Vasconcellos, Perola de Castro ;
de Almeida Pereira, Daniela Cristina ;
da Conceicao, Paulo Roberto ;
Nascimento Saldiva, Paulo Hilario ;
Mauad, Thais ;
Macchione, Mariangela .
SCIENTIFIC REPORTS, 2020, 10 (01)
[8]   IL-1 pathways in inflammation and human diseases [J].
Gabay, Cem ;
Lamacchia, Celine ;
Palmer, Gaby .
NATURE REVIEWS RHEUMATOLOGY, 2010, 6 (04) :232-241
[9]  
Guzik TJ, 2003, J PHYSIOL PHARMACOL, V54, P469
[10]   Lipopolysaccharide activates nuclear factor-KappaB through toll-like receptors and related molecules in cultured biliary epithelial cells [J].
Harada, K ;
Ohira, S ;
Isse, K ;
Ozaki, S ;
Zen, Y ;
Sato, Y ;
Nakanuma, Y .
LABORATORY INVESTIGATION, 2003, 83 (11) :1657-1667