Jin Yuanyuan, Zhang Jiabin, Chen Xiaodie, Li Fenfang, Xue Tiantian, Yi Ke, Xu Yanteng, Wang Haixia, Lao Yeh-Hsing, Chan Hon Fai, Shao Dan, Li Mingqiang, Tao Yu
Laboratory of Biomaterials and Translational Medicine, Center for Nanomedicine, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China; Department of Gastroenterology, The Third Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510630, China.
Laboratory of Biomaterials and Translational Medicine, Center for Nanomedicine, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China.
Biomaterials. 2025 Apr;315:122895. doi: 10.1016/j.biomaterials.2024.122895. Epub 2024 Oct 19.
Acute liver failure (ALF) is a highly fatal disease, necessitating the advancement and optimization of alternative therapeutic strategies to benefit patients awaiting liver transplantation. In this study, we innovatively established the antioxidant nanozyme-hepatocyte-like cells (HLCs) microtissue sheets (HS/N-Au@composite) for ALF therapy. We first prepared a 3D-printed hyaluronic acid/gelatin/sodium alginate scaffold with N-acetylcysteine (NAC)-capped gold nanoclusters (NAC-Au NCs), forming the N-Au@hydrogel. For the encapsulation of HLC spheroids, we used a biocompatible hybrid hydrogel composed of decellularized extracellular matrix (dECM), thrombin, and fibrinogen, resulting in the HS@dECM hydrogel. Utilizing 3D printing technology, we integrated the N-Au@hydrogel with the HS@dECM hydrogel to create the HS/N-Au@composite for in situ transplantation to treat ALF. Our results demonstrated that NAC-Au NCs effectively mitigated reactive oxygen species (ROS)-induced liver necrosis in ALF. Additionally, the N-Au@hydrogel provided mechanical support, ensuring the proper landing and effective functioning of the transplanted HLC spheroids. The HS/N-Au@composite synergistically decreased serum transaminase levels, reduced the accumulation of pro-inflammatory cytokines, accelerated liver function recovery, and promoted liver regeneration in ALF treatment. This combination of HLC spheroids and NAC-Au NCs nanozymes via 3D-printed composite scaffolds represents a promising strategy for enhancing hepatocyte transplantation and advancing stem cell regenerative medicine in ALF therapy.
急性肝衰竭(ALF)是一种高致死性疾病,因此需要推进并优化替代治疗策略,以使等待肝移植的患者受益。在本研究中,我们创新性地构建了用于ALF治疗的抗氧化纳米酶-类肝细胞(HLCs)微组织片(HS/N-Au@复合材料)。我们首先制备了一种3D打印的透明质酸/明胶/海藻酸钠支架,并将其与N-乙酰半胱氨酸(NAC)封端的金纳米簇(NAC-Au NCs)相结合,形成N-Au@水凝胶。为了封装HLC球体,我们使用了一种由脱细胞细胞外基质(dECM)、凝血酶和纤维蛋白原组成的生物相容性混合水凝胶,得到了HS@dECM水凝胶。利用3D打印技术,我们将N-Au@水凝胶与HS@dECM水凝胶整合,制备出HS/N-Au@复合材料用于原位移植治疗ALF。我们的结果表明,NAC-Au NCs有效减轻了ALF中活性氧(ROS)诱导的肝坏死。此外,N-Au@水凝胶提供了机械支撑,确保移植的HLC球体能够正确着床并有效发挥功能。HS/N-Au@复合材料在ALF治疗中协同降低了血清转氨酶水平,减少了促炎细胞因子的积累,加速了肝功能恢复,并促进了肝再生。通过3D打印复合支架将HLC球体与NAC-Au NCs纳米酶相结合,代表了一种在ALF治疗中增强肝细胞移植和推进干细胞再生医学的有前景的策略。