{"title":"肾细胞源性基质中的胶原蛋白 IV 组装受流体流动的影响","authors":"","doi":"10.1016/j.cdev.2024.203923","DOIUrl":null,"url":null,"abstract":"<div><p>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 <em>COL4A2</em> 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 <em>P4HA1</em> 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 <em>in vitro</em> system for investigating flow-induced matrix alteration in the context of kidney development and disease.</p></div>","PeriodicalId":36123,"journal":{"name":"Cells and Development","volume":"179 ","pages":"Article 203923"},"PeriodicalIF":3.9000,"publicationDate":"2024-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S266729012400024X/pdfft?md5=31aac5f90f4486208605930cc23b13db&pid=1-s2.0-S266729012400024X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Collagen IV assembly is influenced by fluid flow in kidney cell-derived matrices\",\"authors\":\"\",\"doi\":\"10.1016/j.cdev.2024.203923\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>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 <em>COL4A2</em> 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 <em>P4HA1</em> 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 <em>in vitro</em> system for investigating flow-induced matrix alteration in the context of kidney development and disease.</p></div>\",\"PeriodicalId\":36123,\"journal\":{\"name\":\"Cells and Development\",\"volume\":\"179 \",\"pages\":\"Article 203923\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2024-04-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S266729012400024X/pdfft?md5=31aac5f90f4486208605930cc23b13db&pid=1-s2.0-S266729012400024X-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cells and Development\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S266729012400024X\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Biochemistry, Genetics and Molecular Biology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cells and Development","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S266729012400024X","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
摘要
肾脏荚膜细胞和内皮细胞组装出复杂而动态的基底膜,这对肾脏过滤至关重要。虽然这种特殊基质的许多成分已为人所知,但人们对流体流动对其组装和组织的影响仍然知之甚少。通过在低剪切应力、高流动生物反应器中培养荚膜细胞和肾小球内皮细胞,我们研究了层流对细胞衍生基质的组成和组装的影响。通过免疫荧光和基质图像分析,我们发现了流动介导的胶原蛋白 IV 重塑。通过对细胞衍生基质的蛋白质组分析,我们确定了流动条件下基质蛋白丰度和组成的变化,包括胶原修饰酶脯氨酰 4-羟化酶(P4HA1)。为了跟踪胶原蛋白 IV 的组装,我们使用 CRISPR-Cas9 将发光标记 HiBiT 敲入荚膜细胞的内源性 COL4A2 基因。通过该系统,我们发现胶原蛋白 IV 在静态和流动条件下都能持续分泌和积累。然而,在荚膜细胞中敲除 P4HA1 会导致胶原蛋白 IV 的分泌减少,而且在流动条件下更为明显。总之,这项工作证明了流体流动对肾脏细胞衍生基质的组成、修饰和组织的影响,并为研究肾脏发育和疾病背景下流动诱导的基质改变提供了一个体外系统。
Collagen IV assembly is influenced by fluid flow in kidney cell-derived matrices
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.