Comparison of Ag-NORs stain and [3H]thymidine incorporation in antiproliferative effect of caffeine on NIH3T3 cells |
Sung-ho Kim1, Cha-soo Lee2 |
1Korea Cancer Center Hospital, Korea Atomic Energy Research Institute 2College of Veterinary Medicine, Kyungpook National University |
Ag-NORs 염색법과 [3H]thymidine incorporation법에 의한 caffeine의 NIH3T3 세포증식 억제효과 비교측정 |
김성호1, 이차수2 |
1한국원자력연구소 원자력병원 2경북대학교 수의과대학 |
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Abstract |
Inhibitory effect of caffeine on NIH3T3 cell proliferation was studied by using [$^3H$]thymidine incorporation and a modified one-step silver staining technique. The latter technique shows argyrophilic nucleolar organizer region-associated proteins (Ag-NORs), which are seen in nuclei as black dots. The result was compared with the counts of [$^3H$] thymidine incorporation. The results were summarized as follows; 1. The Ag-NORs numbers of NIH3T3 cells were $6.81{pm}1.38$ at 24 hrs, $7.13{pm}1.26$ at 48 hrs, $8.50{pm}2.04$ at 72 hrs after incubation. 2. The numbers of Ag-NORs were significantly decrease in caffeine treated groups (p<0.01). 3. The counts of [$^3H$] thymidine incorporation were similar to the result of using Ag-NORs staining technique. It is concluded that Ag-NOR is a rapid, simple and compatible method to quantitate cell proliferation as compared with [$^3H$]thymidine incorporation. |
Key Words:
Ag-NOR, caffeine, NIH3T3, [$^3H$]thymidine incorporation, cell proliferation |
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