An anti-DR5 antibody-curcumin conjugate for the enhanced clearance of activated hepatic stellate cells

肝星状细胞 姜黄素 结合 抗体 化学 细胞凋亡 肝纤维化 癌症研究 纤维化 免疫学 药理学 生物化学 生物 医学 病理 数学分析 数学
作者
Van Quy Nguyen,Dong Gil You,Chan Ho Kim,Seunglee Kwon,Wooram Um,Bong Ryoul Oh,Jae Yoon An,Jueun Jeon,Jae Hyung Park
出处
期刊:International Journal of Biological Macromolecules [Elsevier]
卷期号:192: 1231-1239 被引量:2
标识
DOI:10.1016/j.ijbiomac.2021.09.176
摘要

Anti-death receptor 5 (DR5) antibody is a potential therapeutic agent for liver fibrosis because it exhibits anti-fibrotic effects by inducing the apoptosis of activated hepatic stellate cells (HSCs), which are responsible for hepatic fibrogenesis. However, the clinical applications of anti-DR5 antibodies have been limited by their low agonistic activity against DR5. In this study, an anti-DR5 antibody-curcumin conjugate (DCC) was prepared to investigate its effect on the clearance of activated HSCs. The DCC was synthesized through a coupling reaction between a maleimide-functionalized curcumin derivative and a thiolated anti-DR5 antibody. No significant differences were observed in the uptake behaviors of activated HSCs between the bare anti-DR5 antibodies and DCC. Owing to the antioxidant and anti-inflammatory effects of curcumin, DCC-treated HSCs produced much lower levels of reactive oxygen species and inducible nitric oxide synthase than the bare anti-DR5 antibody-treated HSCs. Additionally, the anti-fibrotic effects of DCC on activated HSCs were more prominent than those of the bare anti-DR5 antibodies, as demonstrated by the immunocytochemical analysis of α-smooth muscle actin. DCC preferentially accumulated in the liver after its systemic administration to mice with liver fibrosis. Thus, DCC may serve as a potential therapeutic agent for treating liver fibrosis.
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