转化式学习
生殖医学
疾病
生殖系统
生物
微生物群
女性生殖系统
生物医学
生殖生物学
系统生物学
盆腔炎
风险分析(工程)
不育
子宫内膜异位症
人类生殖
工程伦理学
辅助生殖技术
医学
生殖技术
生殖内分泌与不孕症
生殖免疫学
人类疾病
生物信息学
转化研究
机制(生物学)
数据科学
心理干预
计算机科学
作者
Pan Min,Huike Chen,Kai Deng,Ke Xiao
出处
期刊:Micromachines
[Multidisciplinary Digital Publishing Institute]
日期:2025-09-30
卷期号:16 (10): 1125-1125
被引量:21
摘要
The female reproductive system represents a highly complex regulatory network governing critical physiological functions, encompassing reproductive capacity and endocrine regulation that maintains female physiological homeostasis. The in vitro simulation system provides a novel tool for biomedical research and can be used as physiological and pathological models to study the female reproductive system. Recent advances in this technology have evolved from 2D and 3D printing to organ-on-a-chip (OOC) and microfluidic systems, which has emerged as a transformative platform for modeling the female reproductive system. These microphysiological systems integrate microfluidics, 3D cell culture, and biomimetic scaffolds to replicate key functional aspects of reproductive organs and tissues. They have enabled precise simulation of hormonal regulation, embryo-endometrium interactions, and disease mechanisms such as endometriosis and gynecologic cancers. This review highlights the current state of female reproductive OOCs, including ovary-, uterus-, and fallopian tube-on-a-chip system, their applications in assisted reproduction and disease modeling, and the technological hurdles to their widespread application. Though significant barriers remain in scaling OOCs for high-throughput drug screening, standardizing protocols for clinical applications, and validating their predictive value against human patient outcomes, OOCs have emerged as a transformative platform to model complex pathologies, offering unprecedented insights into disease mechanisms and personalized therapeutic interventions. Future directions, including multi-organ integration for systemic reproductive modeling, incorporation of microbiome interactions, and clinical translation for mechanisms of drug action, will facilitate unprecedented insights into reproductive physiology and pathology.
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