基于子宫组织工程的子宫内膜异位症类器官研究综述

Zeinan Nurian, Alireza Ebrahimzadeh, Fatemeh Alipour, Hengameh Dortaj
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引用次数: 0

摘要

子宫内膜异位症是一种慢性疾病,与子宫内膜相似的组织在子宫外生长,影响5-10%的女性,导致盆腔疼痛、痛经和不孕。子宫内膜疾病会导致各种生殖健康问题,包括不孕症、不规则出血和子宫内膜癌。研究人员已经开发出先进的体外系统,使用子宫类器官和脱细胞组织支架来理解和模拟这些疾病。传统二维单层培养的主要局限性包括生物活性降低、激素反应性降低以及与ECM缺乏相互作用。研究人员已经研究了3D培养方法来解决这些缺点,例如无支架类器官和脱细胞组织支架。类器官系统可以更好地概括天然子宫内膜的细胞异质性和生理功能。脱细胞方案已被优化,以产生完整的子宫支架,保留ECM的结构和组成特征。将这些生物支架植入动物模型,证明了它们的生物相容性和再生潜力。类器官和支架技术的进一步改进,包括化学定义的基质和器官芯片平台,将提高我们模拟子宫的能力。将这些先进的体外模型与患者来源的细胞相结合,将使个性化疾病建模和靶向治疗的开发成为可能。类器官、去细胞支架和微流控技术的结合在探索生殖生物学、药物筛选以及开发子宫疾病和不孕症的再生疗法方面具有巨大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Insights into Endometriosis Organoids Based on Uterine Tissue Engineering: A Mini-review.

Endometriosis is a chronic condition where tissue similar to the endometrium grows outside the uterus, affecting 5-10% of women and causing pelvic pain, painful periods, and infertility. Diseases of the endometrium, the lining of the uterus, can lead to a variety of reproductive health issues, including infertility, irregular bleeding, and endometrial cancer. Researchers have developed advanced in vitro systems using uterine organoids and decellularized tissue scaffolds to understand and model these diseases. The main limitations of traditional 2D monolayer cultures include reduced biological activity, reduced hormone responsiveness, and lack of interaction with ECM. Researchers have investigated 3D culture approaches to address these shortcomings, such as scaffold-free organoids and decellularized tissue scaffolds. Organoid systems can better recapitulate the cellular heterogeneity and physiological functions of the native endometrium. Decellularization protocols have been optimized to generate intact uterine scaffolds that preserve the structural and compositional features of the ECM. Implantation of these bioscaffolds into animal models demonstrated their biocompatibility and regenerative potential. Further refinements of organoid and scaffold technologies, including chemically defined matrices and organ-on-a-chip platforms, will improve our ability to model the uterus. Integration of these advanced in vitro models with patient-derived cells will enable personalized disease modeling and the development of targeted therapies. The combination of organoids, decellularized scaffolds, and microfluidic technologies holds great potential for exploring reproductive biology, drug screening, and developing regenerative therapies for uterine diseases and infertility.

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