Wellcome Centre for Cell-Matrix Research, School of Biological Science, Faculty of Biology, Medicine and Health, University of Manchester, UK.
Wellcome Centre for Cell-Matrix Research, School of Biological Science, Faculty of Biology, Medicine and Health, University of Manchester, UK.
Cells Dev. 2024 Sep;179:203923. doi: 10.1016/j.cdev.2024.203923. Epub 2024 Apr 24.
Kidney podocytes and endothelial cells assemble a complex and dynamic basement membrane that is essential for kidney filtration. Whilst many components of this specialised matrix are known, the influence of fluid flow on its assembly and organisation remains poorly understood. Using the coculture of podocytes and glomerular endothelial cells in a low-shear stress, high-flow bioreactor, we investigated the effect of laminar fluid flow on the composition and assembly of cell-derived matrix. With immunofluorescence and matrix image analysis we found flow-mediated remodelling of collagen IV. Using proteomic analysis of the cell-derived matrix we identified changes in both abundance and composition of matrix proteins under flow, including the collagen-modifying enzyme, prolyl 4-hydroxylase (P4HA1). To track collagen IV assembly, we used CRISPR-Cas9 to knock in the luminescent marker HiBiT to the endogenous COL4A2 gene in podocytes. With this system, we found that collagen IV was secreted and accumulated consistently under both static and flow conditions. However knockdown of P4HA1 in podocytes led to a reduction in the secretion of collagen IV and this was more pronounced under flow. Together, this work demonstrates the effect of fluid flow on the composition, modification, and organisation of kidney cell-derived matrix and provides an in vitro system for investigating flow-induced matrix alteration in the context of kidney development and disease.
足细胞和内皮细胞组装了一个复杂而动态的基底膜,这对于肾脏过滤至关重要。虽然已经了解了这种特殊基质的许多成分,但对于流体流动对其组装和组织的影响仍知之甚少。我们使用低剪切应力、高通量生物反应器中的足细胞和肾小球内皮细胞共培养,研究了层流对细胞衍生基质组成和组装的影响。通过免疫荧光和基质图像分析,我们发现胶原 IV 发生了流动介导的重塑。通过对细胞衍生基质的蛋白质组学分析,我们发现了基质蛋白在流动下的丰度和组成的变化,包括胶原修饰酶脯氨酰 4-羟化酶(P4HA1)。为了跟踪胶原 IV 的组装,我们使用 CRISPR-Cas9 将发光标记物 HiBiT 敲入到足细胞的内源性 COL4A2 基因中。使用这个系统,我们发现胶原 IV 在静态和流动条件下都被持续分泌和积累。然而,在足细胞中敲低 P4HA1 会导致胶原 IV 的分泌减少,而在流动条件下这种减少更为明显。总之,这项工作展示了流体流动对肾脏细胞衍生基质组成、修饰和组织的影响,并提供了一个体外系统,用于研究肾脏发育和疾病背景下的流动诱导基质改变。