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Volume 12

Journal of Molecular and Genetic Medicine

ISSN: 1747-0862

May 21-23, 2018 Barcelona, Spain

&

Integrative Biology

6

th

International Conference on

Genomics and Molecular Biology

10

th

International Conference on

Genomics 2018 and Integrative Biology 2018

May 21-23, 2018

JOINT EVENT

Mussel adhesive protein-conjugated vitronectin (MAP151-V) induces anti-inflammatory activity on

LPS-stimulated macrophages and UVB-irradiated keratinocyte

Kyung Bae Pi

1

, Seul Gee Um

1

, Jung Mo Ahn

1

, Beom Seop Rho

1

, Ki Beom Lee

1

, Sung Gil Park

2

, Ho Jin Kim

1

and

Yoonjin Lee

3

1

Biotechnology & Business Center, Incheon business information Technopark, Incheon, Korea

2

R&D center, Advanced BioTech Co., Ltd, Pilot Plant 12 Gaetbeol-ro, Yeonsu-gu, Incheon, Korea

3

Cosmocos Corporation, Incheon, Korea

S

kin inflammation and dermal injuries is a major clinical problem due to the current therapies limited to established scars

with poor understanding of healing mechanisms. Unique adhesive and biocompatibility properties of mussel adhesive

proteins (MAPs) are known for their great potential in many tissue engineering and biomedical applications. Previously it was

successfully demonstrated that redesigned hybrid type MAP, fb-151, mass produced in gram-negative bacterium Escherichia

coli, could be utilized as a promising adhesive biomaterial. However, the biological activity of vitronectin-bound recombinant

fb-151 has not been established.The aimof this studywas to develop a novel recombinant protein usingMAP and vitronectin and

to elucidate the anti-inflammatory effects of these on macrophages and keratinocytes. We investigated the anti-inflammatory

activities of recombinant fb-151 conjugated vitronectin (MAP151-V). LPS (Lipopolysaccharide) was used as a stimulant for

macrophages and UVB was used as a stimulant for keratinocytes. Macrophages stimulated by LPS increased the expression of

iNOS and COX-2, which are inflammatory factors, while the MAP151-V -treated groups suppressed the expression of iNOS

and COX-2 in a dose-dependent manner. In addition, keratinocyte stimulated with UVB showed reduced expression of iNOS

and COX-2 MAP151-V treatment. Interestingly, in UVB-irradiated keratinocytes, inflammatory cytokines such as IL-1

β

, IL-6

and TNF-αwere significantly reduced by MAP151-V treatment. These results suggest that MAP151-V has a more effective

anti-inflammatory activity on keratinocyte, suggesting its use as a skin inflammation and therapeutic agent of skin..

Biography

Kyung Bae Pi completed his MS from Kyung Hee University, South Korea. He is a Senior Researcher and Project Leader of Incheon Business Information

Technopark, South Korea. He has published more than 14 papers in reputed journals and has been serving as an Editorial Board Member of repute.

kbpi@ibitp.or.kr

Kyung Bae Pi et al., J Mol Genet Med 2018, Volume 12

DOI: 10.4172/1747-0862-C2-028