去细胞化
材料科学
细胞外基质
自愈水凝胶
生物医学工程
肝功能
丙氨酸转氨酶
天冬氨酸转氨酶
化学
生物化学
医学
碱性磷酸酶
酶
内科学
高分子化学
作者
Ebtehal Ahmed,Tarek Saleh,Lina Yu,Su‐Hyeon Song,Kyung‐Mee Park,Hyung Woo Kwak,Heung‐Myong Woo
摘要
Abstract Acute liver failure (ALF) occurs due to severe liver damage that triggers rapid loss of normal liver function. Here, we investigate the usefulness of an injectable liver extracellular matrix (LECM)‐rich hydrogel generated from an optimized decellularization protocol incorporated with silver nanoparticles (AgNPs) as a promising therapy for ALF. First, we optimized a non‐destructive protocol for rat liver decellularization to obtain ECM‐rich well‐preserved scaffold. Then, LECM hydrogel generated from two commonly used decellularization protocols were compared by LECM hydrogel obtained from our optimized protocol. The ALF model was induced by an intraperitoneal (IP) thioacetamide (TAA) injection followed by the IP injection of LECM hydrogel, collagen–AgNP mixture, or LECM hydrogel–AgNP mixture. LECM‐rich scaffold and hydrogel were successfully obtained using our optimized decellularization protocol. Use of the LECM hydrogel–AgNP mixture to treat TAA‐induced ALF greatly improved liver injury and histological liver regeneration. Interleukin‐6 and transforming growth factor‐beta expressions were significantly reduced, while albumin, hepatocyte growth factor, and Ki67‐positive cells were highly expressed. Moreover, aspartate transaminase and alanine transaminase plasma levels and liver homogenate nitric oxide level were significantly lowered. In conclusion, the LECM hydrogel–AgNP mixture has potential efficient therapeutic and regenerative effects on TAA‐induced liver injury.
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