NSF Science and Technology Center for Engineering Mechanobiology, Washington University in St. Louis, St. Louis, MO, USA.
Department of Mechanical Engineering and Materials Science, Washington University in St. Louis, St. Louis, MO, USA.
Sci Adv. 2022 Sep 2;8(35):eabn6027. doi: 10.1126/sciadv.abn6027. Epub 2022 Aug 31.
Chronic kidney diseases are widespread and incurable. The biophysical mechanisms underlying them are unclear, in part because material systems for reconstituting the microenvironment of relevant kidney cells are limited. A critical question is how kidney podocytes (glomerular epithelial cells) regenerate foot processes of the filtration apparatus following injury. Recently identified sarcomere-like structures (SLSs) with periodically spaced myosin IIA and synaptopodin appear in injured podocytes in vivo. We hypothesized that SLSs template synaptopodin in the initial stages of recovery in response to microenvironmental stimuli and tested this hypothesis by developing an ex vivo culture system that allows control of the podocyte microenvironment. Results supported our hypothesis. SLSs in podocytes that migrated from isolated kidney glomeruli presented periodic synaptopodin-positive clusters that nucleated peripheral, foot process-like extensions. SLSs were mechanoresponsive to actomyosin inhibitors and substrate stiffness. Results suggest SLSs as mechanobiological mediators of podocyte recovery and as potential targets for therapeutic intervention.
慢性肾脏病广泛存在且无法治愈。其背后的生物物理机制尚不清楚,部分原因是用于重建相关肾细胞微环境的物质系统有限。一个关键问题是,在受到损伤后,肾脏足细胞(肾小球上皮细胞)如何再生滤过装置的足突。最近在体内受损的足细胞中发现了具有周期性间隔的肌球蛋白 IIA 和突触蛋白的类似肌节结构(SLSs)。我们假设 SLSs 在受到微环境刺激的恢复初期为突触蛋白提供模板,并通过开发一种允许控制足细胞微环境的体外培养系统来验证这一假设。结果支持了我们的假设。从分离的肾脏肾小球迁移而来的足细胞中的 SLSs 呈现出周期性的突触蛋白阳性簇,这些簇核生出周边的、类似于足突的延伸。SLSs 对肌动球蛋白抑制剂和基质硬度具有机械响应性。结果表明 SLSs 是足细胞恢复的机械生物学介质,也是治疗干预的潜在靶点。