| Budget Amount *help |
¥19,370,000 (Direct Cost: ¥14,900,000、Indirect Cost: ¥4,470,000)
Fiscal Year 2013: ¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2012: ¥6,890,000 (Direct Cost: ¥5,300,000、Indirect Cost: ¥1,590,000)
Fiscal Year 2011: ¥7,410,000 (Direct Cost: ¥5,700,000、Indirect Cost: ¥1,710,000)
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| Research Abstract |
We think of a mouse system in which not gene but protein is destroyed. In this study, we tried to eliminate BP180 in keratinocytes. First, we generated an expression vector BP180 with resolving TAG driven by K14 promoter. TIR gene was introduced to keratinocyte and a keratinocyte line which express TIR gene permanently was established. Expression of TIR gene was examined by western blot and immunofluorescence. Next, we introduced TAG-BP180 construct to those cells and add auxin to culture medium. We found decrease of BP180 expression. This study suggest that this system may provide new diagnosis methods and new treatments for junctional epidermolysis and bullous pemphigoid.
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