Inceptor counteracts insulin signalling in beta-cells to control glycaemia

Resistance to insulin and insulin-like growth factor 1 (IGF1) in pancreatic beta-cells causes overt diabetes in mice; thus, therapies that sensitize beta-cells to insulin may protect patients with diabetes against beta-cell failure(1-3). Here we identify an inhibitor of insulin receptor (INSR) and IGF1 receptor (IGF1R) signalling in mouse beta-cells, which we name the insulin inhibitory receptor (inceptor; encoded by the gene Iir). Inceptor contains an extracellular cysteine-rich domain with similarities to INSR and IGF1R(4), and a mannose 6-phosphate receptor domain that is also found in the IGF2 receptor (IGF2R)(5). Knockout mice that lack inceptor (Iir(-/-)) exhibit signs of hyperinsulinaemia and hypoglycaemia, and die within a few hours of birth. Molecular and cellular analyses of embryonic and postnatal pancreases from Iir(-/-) mice showed an increase in the activation of INSR-IGF1R in Iir(-/-) pancreatic tissue, resulting in an increase in the proliferation and mass of beta-cells. Similarly, inducible beta-cell-specific Iir(-/-) knockout in adult mice and in ex vivo islets led to an increase in the activation of INSR-IGF1R and increased proliferation of beta-cells, resulting in improved glucose tolerance in vivo. Mechanistically, inceptor interacts with INSR-IGF1R to facilitate clathrin-mediated endocytosis for receptor desensitization. Blocking this physical interaction using monoclonal antibodies against the extracellular domain of inceptor resulted in the retention of inceptor and INSR at the plasma membrane to sustain the activation of INSR-IGF1R in beta-cells. Together, our findings show that inceptor shields insulin-producing beta-cells from constitutive pathway activation, and identify inceptor as a potential molecular target for INSR-IGF1R sensitization and diabetes therapy.

  • Ansarullah,
  • Jain, C.
  • Far, F. F.
  • Homberg, S.
  • Wissmiller, K.
  • von Hahn, F. G.
  • Raducanu, A.
  • Schirge, S.
  • Sterr, M.
  • Bilekova, S.
  • Siehler, J.
  • Wiener, J.
  • Oppenlander, L.
  • Morshedi, A.
  • Bastidas-Ponce, A.
  • Collden, G.
  • Irmler, M.
  • Beckers, J.
  • Feuchtinger, A.
  • Grzybek, M.
  • Ahlbrecht, C.
  • Feederle, R.
  • Plettenburg, O.
  • Muller, T. D.
  • Meier, M.
  • Tschop, M. H.
  • Coskun, U.
  • Lickert, H.

Keywords

  • Animals
  • Blood Glucose/analysis/*metabolism
  • Cell Line
  • Cell Proliferation/drug effects
  • Cell Size
  • Clathrin/metabolism
  • Endocrine Cells/metabolism
  • Endocytosis
  • Endoplasmic Reticulum/metabolism
  • Glucose Tolerance Test
  • Golgi Apparatus/metabolism
  • Humans
  • Insulin/*metabolism
  • Insulin Antagonists/*metabolism
  • Insulin-Like Growth Factor I/metabolism
  • Insulin-Secreting Cells/cytology/drug effects/*metabolism
  • Lysosomes/metabolism
  • Male
  • Mice
  • Neoplasm Proteins/chemistry/*metabolism
  • Receptor, Insulin/metabolism
  • *Signal Transduction/drug effects
  • Tamoxifen/pharmacology
Publication details
DOI: 10.1038/s41586-021-03225-8
Journal: Nature
Pages: 326-331
Number: 7845
Work Type: Original
Access number: 33505018
See publication on PubMed
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