4.5 Article

VPS34-dependent control of apical membrane function of proximal tubule cells and nutrient recovery by the kidney

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SCIENCE SIGNALING
卷 15, 期 762, 页码 -

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/scisignal.abo7940

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资金

  1. DFG [RI 2811/1-1, RI 2811/2-1, FOR2743, CRC 877, CRC 1192, GR 3933/1-1, HU 1016/8-2, HU 1016/11-1, HU 1016/12-1]
  2. Novo Nordisk Foundation [NNF19OC0056043]
  3. Carlsberg Foundation
  4. Arhus Universitet frie forskningsfond
  5. Helmut Horten Foundation
  6. BMBF [STOPFSGS-01GM1901C, NephrESA-031L0191E]
  7. Else-Kroner Fresenius Foundation (Else Kroner-Promotionskolleg-iPRIME)
  8. H2020-IMI2 consortium BEAt-DKD [115974]
  9. European Union's Horizon 2020 research and innovation program
  10. EFPIA
  11. JDRF
  12. MICHR training grant [LT1]
  13. Marie-Slodowska Curie global fellowship [GA-841247]
  14. European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant [754513]
  15. Aarhus University Research Foundation
  16. Lundbeck Foundation [R335-2019-2138]
  17. Brodrene Hartman Fond
  18. Horslev Fond
  19. NIH [NCATS UG3TR003288]
  20. University of Michigan O'Brien Kidney Translational Core Center [5P30 DK081943-12]

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This study reveals that lipid kinase VPS34 plays important roles in controlling metabolism, endocytosis, autophagy, and antiviral responses in proximal tubule cells in the kidney. The deficiency of VPS34 leads to alterations in the metabolome, membrane recycling, and fuel utilization, as well as an antiviral response. The findings provide insights into the function of VPS34 in kidney cells and its potential implications in diseases such as cancer and metabolic disorders.
The lipid kinase VPS34 orchestrates autophagy, endocytosis, and metabolism and is implicated in cancer and metabolic disease. The proximal tubule in the kidney is a key metabolic organ that controls reabsorption of nutrients such as fatty acids, amino acids, sugars, and proteins. Here, by combining metabolomics, proteomics, and phosphoproteomics analyses with functional and superresolution imaging assays of mice with an inducible deficiency in proximal tubular cells, we revealed that VPS34 controlled the metabolome of the proximal tubule. In addition to inhibiting pinocytosis and autophagy, VPS34 depletion induced membrane exocytosis and reduced the abundance of the retromer complex necessary for proper membrane recycling and lipid retention, leading to a loss of fuel and biomass. Integration of omics data into a kidney cell metabolomic model demonstrated that VPS34 deficiency increased beta-oxidation, reduced gluconeogenesis, and enhanced the use of glutamine for energy consumption. Furthermore, the omics datasets revealed that VPS34 depletion triggered an antiviral response that included a decrease in the abundance of apically localized virus receptors such as ACE2. VPS34 inhibition abrogated SARS-CoV-2 infection in human kidney organoids and cultured proximal tubule cells in a glutamine-dependent manner. Thus, our results demonstrate that VPS34 adjusts endocytosis, nutrient transport, autophagy, and antiviral responses in proximal tubule cells in the kidney.

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