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Collagen IV assembly is influenced by fluid flow in kidney cell-derived matrices.
Tian, Pinyuan; Koudis, Nikki-Maria; Morais, Mychel R P T; Pickard, Adam; Fresquet, Maryline; Adamson, Antony; Derby, Brian; Lennon, Rachel.
Afiliação
  • Tian P; Wellcome Centre for Cell-Matrix Research, School of Biological Science, Faculty of Biology, Medicine and Health, University of Manchester, UK. Electronic address: pinyuan.tian@manchester.ac.uk.
  • Koudis NM; Wellcome Centre for Cell-Matrix Research, School of Biological Science, Faculty of Biology, Medicine and Health, University of Manchester, UK.
  • Morais MRPT; Wellcome Centre for Cell-Matrix Research, School of Biological Science, Faculty of Biology, Medicine and Health, University of Manchester, UK. Electronic address: mychel.morais@manchester.ac.uk.
  • Pickard A; Wellcome Centre for Cell-Matrix Research, School of Biological Science, Faculty of Biology, Medicine and Health, University of Manchester, UK.
  • Fresquet M; Wellcome Centre for Cell-Matrix Research, School of Biological Science, Faculty of Biology, Medicine and Health, University of Manchester, UK. Electronic address: Maryline.Fresquet@manchester.ac.uk.
  • Adamson A; Genome Editing Unit Core Facility, Faculty of Biology, Medicine and Health, University of Manchester, UK. Electronic address: Antony.Adamson@manchester.ac.uk.
  • Derby B; School of Materials, University of Manchester, UK. Electronic address: Brian.Derby@manchester.ac.uk.
  • Lennon R; Wellcome Centre for Cell-Matrix Research, School of Biological Science, Faculty of Biology, Medicine and Health, University of Manchester, UK; Royal Manchester Children's Hospital, Manchester, UK. Electronic address: Rachel.Lennon@manchester.ac.uk.
Cells Dev ; : 203923, 2024 Apr 24.
Article em En | MEDLINE | ID: mdl-38670459
ABSTRACT
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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article