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Effect of silk fibroin peptide derived from silkworm Bombyx mori on the anti-inflammatory effect of Tat-SOD in a mice edema modelopen access

Authors
Kim, DW[Kim, Dae Won]Hwang, HS[Hwang, Hyun Sook]Kim, DS[Kim, Duk-Soo]Sheen, SH[Sheen, Seung Hoon]Heo, DH[Heo, Dong Hwa]Hwang, G[Hwang, Gyojun]Kang, SH[Kang, Suk Hyung]Kweon, H[Kweon, HaeYong]Jo, YY[Jo, You-Young]Kang, SW[Kang, Seok Woo]Lee, KG[Lee, Kwang-Gill]Park, KW[Park, Kye Won]Han, KH[Han, Kyu Hyung]Park, J[Park, Jinseu]Eum, WS[Eum, Won Sik]Cho, YJ[Cho, Yong-Jun]Choi, HC[Choi, Hyun Chul]Choi, SY[Choi, Soo Young]
Issue Date
31-Dec-2011
Keywords
Inflammation; Protein therapy; Silk fibroin; Tat-superoxide dismutase; Tpa
Citation
BMB REPORTS, v.44, no.12, pp.787 - 792
Indexed
SCIE
SCOPUS
KCI
Journal Title
BMB REPORTS
Volume
44
Number
12
Start Page
787
End Page
792
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/68085
DOI
10.5483/BMBRep.2011.44.12.787
ISSN
1976-6696
Abstract
We investigated whether silk fibroin peptide derived from the silkworm, Bombyx mori, could inhibit inflammation and enhance the anti-inflammatory activity of Tat-superoxide dismutase (Tat-SOD), which was previously reported to effectively penetrate various cells and tissues and exert anti-oxidative activity in a mouse model of inflammation. Inflammation was induced by topical treatment of mouse ears with 12-O-tetradecanoylphorbol-13-acetate (TPA). Histological, Western blot, and reverse transcription-polymerase chain reaction data demonstrated that silk fibroin peptide or Tat-SOD alone could suppress elevated levels of cyclooxygenase-2, interleukin-6, interleukin-1beta, and tumor necrosis factor-alpha induced by TPA. Moreover, silk fibroin peptide significantly enhanced the anti-inflammatory activity of Tat-SOD, although it had no influence on in vitro and in vivo transduction of Tat-SOD. Silk fibroin peptide exhibited anti-inflammatory activity in a mice model of inflammation. Therefore, silk fibroin peptide alone or in combination with Tat-SOD might be used as a therapeutic agent for various inflammatory diseases. [BMB reports 2011; 44(12): 787-792]
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