足细胞
斑马鱼
计算生物学
生物
肾小球
工作流程
核糖核酸
表型
肾
生物信息学
计算机科学
可扩展性
肾脏疾病
细胞生物学
肾小球
功能(生物学)
人类疾病
多囊肾病
神经科学
糖尿病肾病
模式生物
肾功能
作者
Maximilian Schindler,Tim Lange,Sophia‐Marie Bach,Soeren S. Lienkamp,Nicole Endlich
标识
DOI:10.1002/advs.202523662
摘要
ABSTRACT Chronic kidney disease affects more than 850 million people worldwide, yet effective treatment strategies remain limited. The glomerulus is the central filtering unit of the kidney and critically depends on the complex 3D architecture of podocytes. As terminally differentiated and essentially non‐regenerative cells, podocytes are highly vulnerable to injury, and their loss is an irreversible factor in kidney function decline. However, their complex morphology has prevented scalable analysis and slowed progress in drug discovery. To overcome these limitations, Glomage was developed as a cross‐species high‐throughput platform for scalable 3D analysis of glomeruli. In zebrafish larvae, the workflow enables simultaneous isolation, staining, volumetric imaging, and RNA extraction of hundreds of glomeruli. By preserving spatial architecture, the protocol supports rapid, reproducible quantification of podocyte number and structure, enabling systematic assessment of cellular phenotypes at an unprecedented scale. To extend translational relevance, the workflow was adapted to isolated mouse glomeruli, enabling rapid 3D imaging and sensitive detection of key pathological features such as age‐related podocyte depletion. Compatibility across species underscores the robustness, versatility, and broad applicability of the platform. Overall, Glomage creates a powerful high‐content framework for glomerular profiling, accelerates mechanistic studies of podocyte biology, and supports the discovery of urgently needed therapeutic interventions.
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