2013 Fiscal Year Final Research Report
Roles of a cell membrane-nuclear shuttle molecule Hic-5 in skin wound healing
Project/Area Number |
23592647
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Plastic surgery
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Research Institution | Osaka University |
Principal Investigator |
INUI Shigeki 大阪大学, 医学(系)研究科(研究院), 寄附講座准教授 (30324750)
|
Co-Investigator(Kenkyū-buntansha) |
ITAMI Satoshi 大阪大学, 大学院医学系研究科, 寄附講座教授 (30136791)
|
Project Period (FY) |
2011 – 2013
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Keywords | 創傷治癒学 |
Research Abstract |
The immunocytochemistry revealed that Hic-5 shifts from peri-nuclei to cell membrane during keratinocyte differentiation. Using a stable knockdown HaCat keratinocytes (Hic-5KD-HaCat) and control HaCat (cHaCat), in vitro assays revealed that Hic-5 knockdown suppresses DNA synthesis and accelerates migration more than cHaCat. During HaCat keratinocyte differentiation, keratin 1 expression is suppressed in Hic-5KD-HaCat. Regarding adhesion ability to type IV collagen-coated plates, it was suppressed by Hic-5 knockdown. From these results, Hic-5 plays multipotential functions in growth, differentiation, migration and adhesion of human keratinocytes in wound healing. The 16-F1 murine melanoma cells as a model cell line for normal melanocytes were studied likewise, reveling the potential roles of Hic-5 in the proliferation and motility, suggesting its roles in re-pigmentation during wound healing.
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