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The metalloproteinase papp-aa controls epithelial cell quiescence-proliferation transition

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  • Chengdong Liu, University of Michigan, Ann Arbor
  • ,
  • Shuang Li, University of Michigan, Ann Arbor, Xiamen University
  • ,
  • Pernille Rimmer Noer
  • ,
  • Kasper Kjaer-Sorensen
  • Anna Karina Juhl
  • ,
  • Allison Goldstein, University of Michigan, Ann Arbor
  • ,
  • Caihuan Ke, Xiamen University
  • ,
  • Claus Oxvig
  • Cunming Duan, University of Michigan, Ann Arbor

Human patients carrying PAPP-A2 inactivating mutations have low bone mineral density. The underlying mechanisms for this reduced calcification are poorly understood. Using a zebrafish model, we report that Papp-aa regulates bone calcification by promoting Ca2+-transporting epithelial cell (ionocyte) quiescence-proliferation transition. Ionocytes, which are normally quiescent, re-enter the cell cycle under low [Ca2+] stress. Genetic deletion of Papp-aa, but not the closely related Papp-ab, abolished ionocyte proliferation and reduced calcified bone mass. Loss of Papp-aa expression or activity resulted in diminished IGF1 receptor-Akt-Tor signaling in ionocytes. Under low Ca2+ stress, Papp-aa cleaved Igfbp5a. Under normal conditions, however, Papp-aa proteinase activity was suppressed and IGFs were sequestered in the IGF/Igfbp complex. Pharmacological disruption of the IGF/Igfbp complex or adding free IGF1 activated IGF signaling and promoted ionocyte proliferation. These findings suggest that Papp-aa-mediated local Igfbp5a cleavage functions as a [Ca2+]-regulated molecular switch linking IGF signaling to bone calcification by stimulating epithelial cell quiescence-proliferation transition under low Ca2+ stress.

Original languageEnglish
Article numbere52322
Number of pages20
Publication statusPublished - Apr 2020

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