
Materials & Design, Год журнала: 2025, Номер unknown, С. 113900 - 113900
Опубликована: Апрель 1, 2025
Язык: Английский
Materials & Design, Год журнала: 2025, Номер unknown, С. 113900 - 113900
Опубликована: Апрель 1, 2025
Язык: Английский
Chemical Engineering Journal, Год журнала: 2025, Номер unknown, С. 160293 - 160293
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
1Journal of Tissue Engineering, Год журнала: 2025, Номер 16
Опубликована: Янв. 1, 2025
The development of advanced in vitro models for assessing liver toxicity and drug responses is crucial personalized medicine preclinical development. 3D bioprinting technology provides opportunities to create human that are suitable conducting high-throughput screening toxicity. In this study, we fabricated a humanized model using human-induced hepatocytes (hiHeps) derived from fibroblasts via rapid efficient reprogramming process. These hiHeps were then employed bioprinted with bioink materials closely mimic the natural extracellular matrix. constructed livers (h3DPLs) exhibited mature hepatocyte functions, including albumin expression, glycogen storage, uptake/release indocyanine green acetylated low-density lipoprotein. Notably, h3DPLs demonstrated increased sensitivity hepatotoxic agents such as acetaminophen (APAP), making them promising platform studying drug-induced injury. Furthermore, our accurately reflected impact rifampin, cytochrome P450 inducer, on CYP2E1 levels APAP hepatotoxicity. results highlight potential hiHep-based cost-effective high-performance alternative testing, paving way improved strategies therapeutic interventions.
Язык: Английский
Процитировано
0Biomaterials, Год журнала: 2025, Номер unknown, С. 123293 - 123293
Опубликована: Март 1, 2025
Язык: Английский
Процитировано
0Materials & Design, Год журнала: 2025, Номер unknown, С. 113900 - 113900
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
0