Melittin has a chondroprotective effect by inhibiting MMP-1 and MMP-8 expressions via blocking NF-kappa B and AP-1 signaling pathway in chondrocytes
- Authors
- Jeong, Yun-Jeong; Shin, Jae-Moon; Bae, Young-Seuk; Cho, Hyun-Ji; Park, Kwan-Kyu; Choe, Jung-Yoon; Han, Sang-Mi; Moon, Sung-Kwon; Kim, Wun-Jae; Choi, Yung Hyun; Kim, Cheorl-Ho; Chang, Hyeun-Wook; Chang, Young-Chae
- Issue Date
- Apr-2015
- Publisher
- ELSEVIER SCIENCE BV
- Keywords
- Bee venom; Melittin; Chondrocyte; Type II collagen
- Citation
- INTERNATIONAL IMMUNOPHARMACOLOGY, v.25, no.2, pp 400 - 405
- Pages
- 6
- Journal Title
- INTERNATIONAL IMMUNOPHARMACOLOGY
- Volume
- 25
- Number
- 2
- Start Page
- 400
- End Page
- 405
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/9710
- DOI
- 10.1016/j.intimp.2015.02.021
- ISSN
- 1567-5769
1878-1705
- Abstract
- Bee venom is a natural ingredient produced by the honey bee (Apis mellifera), and has been widely used in China, Korea and Japan as a traditional medicine for various diseases such as arthritis, rheumatism, and skin diseases However, the regulation of the underlying molecular mechanisms of the anti-arthritis by bee venom and its major peptides is largely unknown. In this study, we investigated the potential molecular mechanisms underlying the anti-arthritis effect of bee venom and its major peptides, melittin and apamin, in tumor necrosis factor-alpha (TNF-alpha) responsive C57BL/6 mice chondrocyte cells. The bee venom and melittin significantly and selectively suppressed the TNF-alpha-mediated decrease of type II collagen expression, whereas the apamin had no effects on the type II collagen expression. We, furthermore, found that the bee venom and melittin inhibited the protein expression of matrix metalloproteinase (MMP)-1 and MMP-8, which suggests that the chondroprotective effect of bee venom may be caused by melittin. The inhibitory effects of melittin on the TNF-alpha-induced MMP-1 and MMP-8 protein expression were regulated by the inhibition of NF-kappa B and AP-1. In addition, melittin suppressed the TNF-alpha-induced phosphorylation of Akt, JNK and ERK1/2, but did not affect the phosphorylation of p38 kinase. These results suggest that melittin suppresses TNF-alpha-stimulated decrease of type II collagen expression by the inhibiting MMP-1 and MMP-8 through regulation of the NF-kappa B and AP-1 pathway and provision of a novel role for melittin in anti-arthritis action. (C) 2015 Elsevier B.V. All rights reserved.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - ETC > 1. Journal Articles

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.