Evaluation of 18F-SFB-Annexin B1 in detecting apoptosis
10.3760/cma.j.issn.0253-9780.2011.02.010
- VernacularTitle:18F-SFB-Annexin B1探测细胞凋亡实验研究
- Author:
Qing, ZHAO
;
Ying-jian, ZHANG
;
Fang, WANG
;
Yong-ping, ZHANG
;
Jun-yan, XU
;
Zhong-yi, YANG
;
Jing-yi, CHENG
;
Ming-wei, WANG
;
Yue, WANG
;
Shu-han, SUN
- Publication Type:Journal Article
- Keywords:
Annexin B1;
Fluorine radioisotopes;
Apoptosis;
SFB;
Redionuclide imaging;
Rabbits
- From:Chinese Journal of Nuclear Medicine
2011;31(2):112-116
- CountryChina
- Language:Chinese
-
Abstract:
Objective To evaluate 18F-N- succinimidyl -4-fluorobenzoate (SFB)-Annexin B1 in detectingin vitro andin vivo apoptosis. Methods Anti-Fas antibody was used to induce apoptosis in Jurkat cells. Apoptosis in Jurkat cells was confirmed by flow cytometer (FCM). Unilateral renal ischemia/reperfusion injury was induced by transient (45 min) ligation of the renal artery in the rabbit. The rabbit was then administrated with 18F-SFB-Annexin B1 intravenously 24 h later and then imaged by PET/CT at 10,30,60,90,120 and 240 min postinjection. Apoptosis in kidney was confirmed by terminal deoxynucleotidyl transferase mediated dUTP biotin nick end labeling (TUNEL) assay and HE staining. Results The apoptosis rate induced by anti-Fas antibody was 25.98%(120 min) while that in the control group was only 1.81%. The uptake of 18F-SFB-Annexin B1in apoptosis group was greater than that in the control group. PET/CT images at 240 min showed higher uptake in the ligated kidney than the non-ligated kidney. TUNEL assay and HE staining confirmed great amount apoptotic cells in the ligated kidney. Conclusion 18 F-SFB-Annexin B1may be potentially useful in detecting apoptosis both in vitro and in vivo.
