Precise cell therapy for liver fibrosis: Endothelial cell and macrophage therapy

Liping Deng , Bingjie Wu , Kaini Liang, Hongen Liao, Yanan Du
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引用次数: 0

Abstract

Liver fibrosis is typically caused by chronic viral hepatitis and, more recently, fatty liver disease associated with obesity. There are currently no approved drugs for liver cirrhosis, and liver transplantation is limited by donor scarcity, thus driving the investigation of novel therapeutic strategies. The development of liver fibrosis presents with stage- and zone-dependent characteristics that manifest as distinct dynamic changes during vascularization and extracellular matrix (ECM) deposition. However, current cellular therapies do not consider the spatiotemporal variations of liver fibrosis without identifying the precise location and stage to administer the intervention to achieve optimal therapeutic effects. Herein, we focus on endothelial cell (EC) and macrophage therapy for liver fibrosis because of their important roles in regulating the spatiotemporal changes of vascularization and ECM deposition during liver fibrosis progression. Overall, this review summarizes the stage-dependent EC and macrophage therapy for liver fibrosis, elucidates their respective mechanisms, and exemplifies potential strategies to realize precise cell therapy by targeting specific liver zones.

肝纤维化的精确细胞治疗:内皮细胞和巨噬细胞治疗
肝纤维化通常由慢性病毒性肝炎和最近与肥胖相关的脂肪肝引起。目前尚无批准的肝硬化药物,肝移植受供体稀缺的限制,因此推动了新的治疗策略的研究。肝纤维化的发展具有阶段和区域依赖特征,表现为血管化和细胞外基质(ECM)沉积过程中明显的动态变化。然而,目前的细胞疗法没有考虑肝纤维化的时空变化,没有确定精确的位置和阶段来实施干预,以达到最佳的治疗效果。在此,我们将重点放在肝纤维化的内皮细胞(EC)和巨噬细胞治疗上,因为它们在调节肝纤维化进展过程中血管化和ECM沉积的时空变化中起着重要作用。总之,本文总结了肝纤维化的分期依赖性EC和巨噬细胞治疗,阐明了它们各自的机制,并举例说明了通过靶向特定肝脏区域实现精确细胞治疗的潜在策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.60
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