Shaw Claire A, Verstrate Margo, Graniczkowska Kinga, Risoen Katie R, Dini Pouya, Weimer Bart C
School of Veterinary Medicine, Population Health and Reproduction, University of California, Davis, Davis, CA, United States.
100K Pathogen Genome Project, University of California, Davis, Davis, CA, United States.
Front Cell Infect Microbiol. 2025 Aug 20;15:1641366. doi: 10.3389/fcimb.2025.1641366. eCollection 2025.
Stem cells and organoids have emerged as pivotal biological tools for biologically relevant models. Together, these models realistically recapitulate structural and functional elements of the organ, allowing for studies of cellular, molecular, and genetic features that underpin various diseases that are difficult to observe in low-biomass tissues. Stem cells, and more recently organoids, have been applied as regenerative therapies. The emergence of the microbiome as an occupant throughout different body locales requires new approaches to understand the complex cellular interactions with the host tissue at each site. The success of regenerative medicine strategies and therapeutic development is intricately linked to this understanding and management of host-microbe dynamics. Interactions with the host microbiome and infections can both significantly impair tissue regeneration and compromise the function of stem cell-derived therapies. Therefore, a comprehensive understanding of how pathogens and the microbiome interact with stem cells and organoids is relevant for developing safe and effective regenerative medicine interventions. This review explores the evolving landscape of organoid technology, including a discussion on the importance of stem cell studies and considerations for organoid development that are important for use as models to study microbiome interactions. Additionally, this work describes the pivotal role of cell culture models in advancing host-microbe interaction studies in understudied low-biomass organs such as the stomach and reproductive tract. Through this assessment, we aim to shed light on the potential of these models to transform the approach to studying and managing infectious diseases within the context of regenerative medicine.
干细胞和类器官已成为构建生物学相关模型的关键生物学工具。这些模型共同逼真地再现了器官的结构和功能要素,使得对支撑各种疾病的细胞、分子和遗传特征的研究成为可能,而这些特征在低生物量组织中难以观察到。干细胞,以及最近出现的类器官,已被应用于再生疗法。微生物群作为占据不同身体部位的存在,其出现需要新的方法来理解在每个部位与宿主组织的复杂细胞相互作用。再生医学策略和治疗开发的成功与对宿主-微生物动态的理解和管理密切相关。与宿主微生物群的相互作用和感染都可能显著损害组织再生并损害干细胞衍生疗法的功能。因此,全面了解病原体和微生物群如何与干细胞和类器官相互作用,对于开发安全有效的再生医学干预措施至关重要。本综述探讨了类器官技术的发展态势,包括讨论干细胞研究的重要性以及类器官开发的注意事项,这些对于用作研究微生物群相互作用的模型很重要。此外,这项工作描述了细胞培养模型在推进对胃和生殖道等研究较少的低生物量器官中宿主-微生物相互作用研究方面的关键作用。通过这项评估,我们旨在阐明这些模型在再生医学背景下改变传染病研究和管理方法的潜力。