2012 Fiscal Year Final Research Report
Does Epiplakin modulate the malignant feature of tumor?
Project/Area Number |
23791281
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Dermatology
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Research Institution | Oita University |
Principal Investigator |
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Research Collaborator |
FUJIWARA Sakuhei 大分大学, 医学部皮膚科, 教授 (90181411)
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Project Period (FY) |
2011 – 2012
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Keywords | アクチン / エピプラキン / 細胞遊走 / 発現抑制 / HeLa 細胞 |
Research Abstract |
To study the function of EPPK, we developed EPPK knock-down (KD) and EPPK-overexpressing HeLa cells and analyzed cellular phenotypes and motility by fluorescence/ differential interference contrast time-lapse microscopy and immunolocalization of actin and vimentin. Cellular motility of EPPK-KD cells was significantly elevated, but that of EPPK-overexpressing cells was obviously depressed. Many spike-like projections were observed on EPPK-KD cells, with fewer such structures on overexpressing cells. By contrast, in EPPK-KD cells, expression of E-cadherin was unchanged but vimentin fibers were thinner and sparser than in controls, and they were more concentrated at the peri -nucleus, as observed in migrating keratinocytes at wound edges in EPPK-/-mice. Our results suggest that EPPK is associated with the machinery for cellular motility and contributes to tissue architecture via the rearrangement of intermediate filaments.
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Research Products
(3 results)
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[Journal Article] Epiplakin modifies the motility of the HeLa cells and accumulates at the outer surfaces of 3-D cell clusters2013
Author(s)
Shimada H, Nambu-Niibori A, Wilson-Morifuji M, Mizuguchi S, Araki N, Sumiyoshi H, Sato M, Mezaki Y, Senoo H, Ishikawa K, Hatano Y, Okamoto O, Fujiwara S
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Journal Title
J Dermatol
Volume: 40(4)
Pages: 249-58
Peer Reviewed
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