文献类型：期刊文献

中文题名：nhibition of tissue transglutaminase promotes Aβ- nduced apoptosis in SH-SY5Y cells

英文题名：nhibition of tissue transglutaminase promotes Aβ- nduced apoptosis in SH-SY5Y cells

作者：JiZHANG[1,2,3];Yi-rong DING[1];Rui WANG[1]

机构：[1]Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, Shanghai 200237, China;[2]Department of Nuclear Medicine, Fudan University Shanghai Cancer Center, Shanghai 200032, China;[3]Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China

年份：2016

卷号：37

期号：12

起止页码：1534

中文期刊名：Acta Pharmacologica Sinica

外文期刊名：中国药理学报（英文版）

收录：CSTPCD;;Scopus;CSCD:【CSCD2015_2016】；PubMed;

基金：This work was supported by the grants to Rui WANG from the National Natural Science Foundation of China （No 81072627 and 81230090）, the Shanghai Committee of Science and Technology （No 12431900901）, and the 111 Project of the Chinese Ministry of Education （No B07023）.

语种：英文

中文关键词：tissue transglutaminase （tTG）; γ-glutamyl-ε-lysine isopeptide; Alzheimer＇s disease; NTU283; β-amyloid; SH-SY5Y cells;apoptosis

外文关键词：tissue transglutaminase （tTG）; γ-glutamyl-ε-lysine isopeptide; Alzheimer＇s disease; NTU283; β-amyloid; SH-SY5Y cells;apoptosis

摘要：Aim： Tissue transglutaminase （tTG） catalyzes proteins, including β-amyloid （Aβ）, to cross-link as a y-glutamyl-ε-lysine structure isopeptide, which is highly resistant to proteolysis. Thus, tTG plays an important role in protein accumulation in Alzheimer＇s disease （AD）. In the present study, we examined the effect of an irreversible tTG inhibitor, NTU283, on All mimic-induced AD pathogenesis in SH-SY5Y cells.Methods： Western blot and in-cell Western analyses were used to detect tTG and isopeptide （representing the enzyme activity of tTG） protein levels. Moreover, Hoechst and PI co-staining was performed, and caspase-3 and caspase-7 activities and the Bax/Bcl-2 ratio were determined to evaluate the effects of NTU283 on apoptosis. Results： The results confirmed that tTG activity was inhibited by NTU283 20-500 μmol/L in a concentration-dependent manner in SH-SY5Y cells. Contrary to our expectations, however, the isopeptide bonds were increased when cells were co-treated with Aβ and NTU283. In addition, NTU283 alone did not induce apoptosis in SH-SY5Y cells. However, when co-applied with Aβ, NTU283 promoted rather than inhibited Aβ-induced apoptosis. Consistent with the apoptotic rate, pretreating cells with different concentrations of NTU283 and Aβsignificantly increased the activities of caspase-3 and caspase-7 as well as the ratio of Bax/Bcl-2. Conclusion： Irreversible inhibition of tTG activity did not block but rather promoted Aβ-induced apoptosis, which indicated that tTG has complex functions in AD pathogenesis.
Aim： Tissue transglutaminase （tTG） catalyzes proteins, including β-amyloid （Aβ）, to cross-link as a y-glutamyl-ε-lysine structure isopeptide, which is highly resistant to proteolysis. Thus, tTG plays an important role in protein accumulation in Alzheimer＇s disease （AD）. In the present study, we examined the effect of an irreversible tTG inhibitor, NTU283, on All mimic-induced AD pathogenesis in SH-SY5Y cells.Methods： Western blot and in-cell Western analyses were used to detect tTG and isopeptide （representing the enzyme activity of tTG） protein levels. Moreover, Hoechst and PI co-staining was performed, and caspase-3 and caspase-7 activities and the Bax/Bcl-2 ratio were determined to evaluate the effects of NTU283 on apoptosis. Results： The results confirmed that tTG activity was inhibited by NTU283 20-500 μmol/L in a concentration-dependent manner in SH-SY5Y cells. Contrary to our expectations, however, the isopeptide bonds were increased when cells were co-treated with Aβ and NTU283. In addition, NTU283 alone did not induce apoptosis in SH-SY5Y cells. However, when co-applied with Aβ, NTU283 promoted rather than inhibited Aβ-induced apoptosis. Consistent with the apoptotic rate, pretreating cells with different concentrations of NTU283 and Aβsignificantly increased the activities of caspase-3 and caspase-7 as well as the ratio of Bax/Bcl-2. Conclusion： Irreversible inhibition of tTG activity did not block but rather promoted Aβ-induced apoptosis, which indicated that tTG has complex functions in AD pathogenesis.