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Kidney organoids: Research in developmental biology and emerging applications

机译:肾单板:发展生物学和新兴应用中的研究

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Kidney organoids generated from human pluripotent stem cells (hPSCs) have drastically changed the field of stem cell research on human kidneys within a few years. They are self-organizing multicellular structures that contain nephron components such as glomeruli and renal tubules in most cases, but hPSC-derived ureteric buds, the progenitors of collecting ducts and ureters, can also form three-dimensional organoids. Today's challenges facing human kidney organoids are further maturation and anatomical integrity in order to achieve a complete model of the developing kidneys and ultimately a complete adult organ. Since chronic kidney disease (CKD) and impaired kidney function are an increasing burden on public health worldwide, there is an urgent need to develop effective treatments for various renal conditions. In this regard, hPSC-derived kidney organoids may impact medicine by providing new translational approaches. The unique ability of kidney organoids derived from disease-specific hPSCs to reproduce human diseases caused by genetic alterations may help provide the next generation of kidney disease models. Recent advances in the field of kidney organoid research have been generally accompanied by progress in developmental biology and other technological breakthroughs. In this review, we consider the current trends in kidney organoid technology, especially focusing on the relationship to the study of human kidney development, and discuss the remaining hurdles and prospects in regenerating human kidney structures beyond organoids.
机译:由人类多能干细胞(hPSCs)产生的肾脏类器官在几年内彻底改变了人类肾脏干细胞研究领域。它们是自组织的多细胞结构,在大多数情况下包含肾小球和肾小管等肾单位成分,但hPSC衍生的输尿管芽(集合管和输尿管的祖细胞)也可以形成三维类器官。今天,人类肾脏类器官面临的挑战是进一步成熟和解剖完整性,以实现肾脏发育的完整模型,最终形成完整的成人器官。由于慢性肾脏病(CKD)和肾功能受损对全球公共卫生的负担越来越大,因此迫切需要开发针对各种肾脏疾病的有效治疗方法。在这方面,hPSC衍生的肾脏类器官可能通过提供新的转化途径影响医学。来源于疾病特异性HPSC的肾脏类器官复制由基因改变引起的人类疾病的独特能力可能有助于提供下一代肾脏疾病模型。肾脏类器官研究领域的最新进展通常伴随着发育生物学的进展和其他技术突破。在这篇综述中,我们考虑肾器官技术的当前趋势,特别是着眼于与人类肾脏发育研究的关系,并讨论剩余的障碍和前景在再生器官结构之外的人类肾脏结构。

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