| Budget Amount *help |
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2009: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2008: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
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| Research Abstract |
At first, we analyzed in tumor cells of allogeneic transplantation models, because it turned out to require more time beyond our expectation to achieve the clear result of suppressing macrophages from allogeneic organ transplantation mouse models. We have already reported that 3 × 10^6 cells Meth A fibro-sarcoma (MA cells) which were allo-transplantated into peritoneal space of a C57BL/6 mouse completely rejected in about 14 days. We have also reported that allograft-induced macrophages (AIM) were effective mainly as cellular disorder of peritoneal infiltrating which were activated in this rejection. MA cells have been known to be CTL resistant cells. In this study, we used GFP transgenic C57BL/6 mice (GFP-mice) for the donors and we finally succeeded in videotaping that the GFP-AIM were biting off the co-cultured allogeneic MA cells. We were sure that the bited off allo-MA cells from this achievement. But, we now have to solve the critical problems whether biting off abilities of the AIM are exert toward allogeneic or neoplastic changes of MA. Now we are examining the ability of AIM derived from PEC to solve this problem, after removing some AIM cells which can respond to neoplastic changes. In addition, we are investigating time course of fluorescence shift of the cells PEC drive adherent cells mainly consist from GFP-AIM with or without various concentration of some of agents influence to macrophage, like as Tranilast(3μM~300μM). We, however, have not found out critical effect of it yet. Next, we will try it in activation phase of AIM.
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