open access publication

Article, 2023

Compromised junctional integrity phenocopies age-dependent renal dysfunction in Drosophila Snakeskin mutants

Journal of Cell Science, ISSN 1477-9137, 0021-9533, Volume 136, 19, Page jcs261118, 10.1242/jcs.261118

Contributors

Dornan, Anthony J 0000-0002-5228-2893 [1] Halberg, Kenneth Veland 0000-0002-5903-7196 [2] Beuter, Liesa-Kristin 0000-0003-2844-4327 [1] [3] Davies, Shireen-Anne [1] Dow, Julian Alexander 0000-0002-9595-5146 (Corresponding author) [1]

Affiliations

  1. [1] University of Glasgow
  2. [NORA names: United Kingdom; Europe, Non-EU; OECD];
  3. [2] University of Copenhagen
  4. [NORA names: KU University of Copenhagen; University; Denmark; Europe, EU; Nordic; OECD];
  5. [3] University of Giessen
  6. [NORA names: Germany; Europe, EU; OECD]

Abstract

Transporting epithelia provide a protective barrier against pathogenic insults while allowing the controlled exchange of ions, solutes and water with the external environment. In invertebrates, these functions depend on formation and maintenance of 'tight' septate junctions (SJs). However, the mechanism by which SJs affect transport competence and tissue homeostasis, and how these are modulated by ageing, remain incompletely understood. Here, we demonstrate that the Drosophila renal (Malpighian) tubules undergo an age-dependent decline in secretory capacity, which correlates with mislocalisation of SJ proteins and progressive degeneration in cellular morphology and tissue homeostasis. Acute loss of the SJ protein Snakeskin in adult tubules induced progressive changes in cellular and tissue architecture, including altered expression and localisation of junctional proteins with concomitant loss of cell polarity and barrier integrity, demonstrating that compromised junctional integrity is sufficient to replicate these ageing-related phenotypes. Taken together, our work demonstrates a crucial link between epithelial barrier integrity, tubule transport competence, renal homeostasis and organismal viability, as well as providing novel insights into the mechanisms underpinning ageing and renal disease.

Keywords

Renal, SJ, SJ proteins, acute loss, age, age-dependent decline, aging-related phenotypes, architecture, barrier integrity, barriers, capacity, cell polarity, cells, cellular morphology, changes, competence, concomitant loss, controlled exchange, decline, degeneration, disease, dysfunction, environment, epithelia, epithelial barrier integrity, exchange of ions, expression, external environment, formation, function, homeostasis, insult, integration, invertebrates, ions, junction integrity, junction proteins, localisation, loss, maintenance, mechanism, mislocalisation, morphology, organismal viability, pathogenic insults, phenotype, polarization, progressive changes, progressive degeneration, protective barrier, protein, renal disease, renal dysfunction, renal homeostasis, secretory capacity, snakeskin, solution, tissue, tissue architecture, tissue homeostasis, transport, transport competence, transporting epithelia, tubules, viability, water

Funders

  • Danish Agency for Science and Higher Education
  • Biotechnology and Biological Sciences Research Council
  • The Velux Foundations

Data Provider: Digital Science