Abstract
Various bioactivities of the starfish hatching enzyme (HE) including collagen gel contraction, MMPs activity, hydroxyproline release, and gene regulation based on the fibroblast-populated collagen lattice (FPCL) in three-dimensional medium were investigated for the improvement of scar and keloid. The starfish HE significantly inhibited the collagen gel contraction over 2 days of culture. MMP-2 and MMP-9 activities were also identified by gelatin zymography and RT-PCR products with both HE and collagenase treatments, which resulted in the high amount of hydroxyproline release. The HE treatment on the FPCL significantly inhibited the fibroblast proliferation at 3 days of culture. The LPS-induced NO level and iNOS mRNA expression at low concentrations of HE presented a certain ability to inflammatory response. The COX-2 mRNA from the FPCL indicated no significant inflammation-mediated activity at 5 μg/mL of HE, whereas the cytokines of TNF-α and IL-1β were significantly higher than those of the control. Hence, the starfish hatching enzyme can regulate the fibroblast-populated collagen gel conditions by the contraction, MMP production, inflammatory gene expression, etc. Therefore, the starfish HE could be a potential cosmeceutical to heal the scar and keloid tissue.
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Abbreviations
- HE:
-
Hatching enzyme
- ECM:
-
Extracellular matrix
- MMP:
-
Matrix metalloprotease
- TIMP:
-
Tissue inhibitors metalloproteases
- NO:
-
Nitric oxide
- FPCL:
-
Fibroblast-populated collagen lattice
- iNOS:
-
Inducible nitric oxide synthase
- TNF-α:
-
Tumor necrosis factor-alpha
- IL-1β:
-
Interleukin-1 beta
- TGF:
-
Transfer growth factor
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Acknowledgments
This research was supported by the Korea Sea Grant Program (GangWon Sea Grant) funded by the Ministry of Oceans and Fisheries in Korea.
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Li, Z.J., Kim, S.M. The Application of the Starfish Hatching Enzyme for the Improvement of Scar and Keloid Based on the Fibroblast-Populated Collagen Lattice. Appl Biochem Biotechnol 173, 989–1002 (2014). https://doi.org/10.1007/s12010-014-0901-7
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DOI: https://doi.org/10.1007/s12010-014-0901-7