Evaluation of 18F-SFB-Annexin B1 in detecting apoptosis
Qing Zhao, Yingjian Zhang, Fang Wang, Yongping Zhang, Junyan Xu, Zhongyi Yang, Cheng Jingyi, Wang Mingwei, Yue Wang, Sun Shuhan
Abstract
Qing Zhao, Yingjian Zhang, Fang Wang, Yongping Zhang, Junyan Xu, Zhongyi Yang, Cheng Jingyi, Wang Mingwei, Yue Wang, Sun Shuhan
Abstract
:Objective To evaluate18F-N- succinimidyl -4-fluorobenzoate (SFB)-Annexin B1 in detectingin vitro andin vivoapoptosis. Methods Anti-Fas antibody was used to induce apoptosis in Jurkat cells.Apoptosis in Jurkat cells was confirmed by flow cytometer (FCM). Unilateral renalischemia/reperfusion injury was induced by transient (45 min) ligation of the renal arteryin the rabbit. The rabbit was then administrated with 18F-SFB-Annexin B1 intravenously 24h later and then imaged by PET/CT at 10,30,60,90,120 and 240 min postinjection. Apoptosisin kidney was confirmed by terminal deoxynucleotidyl transferase mediated dUTP biotin nickend labeling (TUNEL) assay and HE staining. Results The apoptosis rate induced by anti-Fasantibody was 25.98%(120 min) while that in the control group was only 1.81%. The uptake of18F-SFB-Annexin B1in apoptosis group was greater than that in the control group. PET/CTimages 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 invitro and in vivo.
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:Objective To evaluate18F-N- succinimidyl -4-fluorobenzoate (SFB)-Annexin B1 in detectingin vitro andin vivoapoptosis. Methods Anti-Fas antibody was used to induce apoptosis in Jurkat cells.Apoptosis in Jurkat cells was confirmed by flow cytometer (FCM). Unilateral renalischemia/reperfusion injury was induced by transient (45 min) ligation of the renal arteryin the rabbit. The rabbit was then administrated with 18F-SFB-Annexin B1 intravenously 24h later and then imaged by PET/CT at 10,30,60,90,120 and 240 min postinjection. Apoptosisin kidney was confirmed by terminal deoxynucleotidyl transferase mediated dUTP biotin nickend labeling (TUNEL) assay and HE staining. Results The apoptosis rate induced by anti-Fasantibody was 25.98%(120 min) while that in the control group was only 1.81%. The uptake of18F-SFB-Annexin B1in apoptosis group was greater than that in the control group. PET/CTimages 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 invitro and in vivo.
Key concepts: TUNEL assay, Annexin, Apoptosis, Terminal deoxynucleotidyl transferase, In Situ Nick-End Labeling, Flow cytometry, Molecular biology, In vivo