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  • Khilji, M. S. (author)

The inducible β5i proteasome subunit contributes to proinsulin degradation in GRP94-deficient β-cells and is overexpressed in type 2 diabetes pancreatic islets

  • Article/chapterEnglish2020

Publisher, publication year, extent ...

  • 2020

Numbers

  • LIBRIS-ID:oai:gup.ub.gu.se/297807
  • https://gup.ub.gu.se/publication/297807URI
  • https://doi.org/10.1152/AJPENDO.00372.2019DOI

Supplementary language notes

  • Language:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Proinsulin is a misfolding-prone protein, and its efficient breakdown is critical when β-cells are confronted with high-insulin biosynthetic demands, to prevent endoplasmic reticulum stress, a key trigger of secretory dysfunction and, if uncompensated, apoptosis. Proinsulin degradation is thought to be performed by the constitutively expressed standard proteasome, while the roles of other proteasomes are unknown. We recently demonstrated that deficiency of the proinsulin chaperone glucoseregulated protein 94 (GRP94) causes impaired proinsulin handling and defective insulin secretion associated with a compensated endoplasmic reticulum stress response. Taking advantage of this model of restricted folding capacity, we investigated the role of different proteasomes in proinsulin degradation, reasoning that insulin secretory dynamics require an inducible protein degradation system. We show that the expression of only one enzymatically active proteasome subunit, namely, the inducible β5i-subunit, was increased in GRP94 CRISPR/Cas9 knockout (KO) cells. Additionally, the level of β5i-containing intermediate proteasomes was significantly increased in these cells, as was β5i-related chymotrypsin-like activity. Moreover, proinsulin levels were restored in GRP94 KO upon β5i small interfering RNA-mediated knockdown. Finally, the fraction of β-cells expressing the β5i subunit is increased in human islets from type 2 diabetes patients. We conclude that β5i is an inducible proteasome subunit dedicated to the degradation of mishandled proinsulin. Copyright © 2020 the American Physiological Society.

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Added entries (persons, corporate bodies, meetings, titles ...)

  • Bresson, S. E. (author)
  • Verstappen, D. (author)
  • Pihl, C. (author)
  • Andersen, P. A. K. (author)
  • Agergaard, J. B. (author)
  • Dahlby, T. (author)
  • Bryde, T. H. (author)
  • Klindt, K. (author)
  • Nielsen, C. K. (author)
  • Walentinsson, A. (author)
  • Zivkovic, D. (author)
  • Bousquet, M. P. (author)
  • Tyrberg, BjörnGothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology (author)
  • Richardso, S. J. (author)
  • Morga, N. G. (author)
  • Mandrup-Poulsen, T. (author)
  • Marzec, M. T. (author)
  • Göteborgs universitetInstitutionen för neurovetenskap och fysiologi, sektionen för fysiologi (creator_code:org_t)

Related titles

  • In:American Journal of Physiology - Endocrinology and Metabolism318:60193-1849

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