Role of iRhoms 1 and 2 in Endochondral Ossification

Int J Mol Sci. 2020 Nov 19;21(22):8732. doi: 10.3390/ijms21228732.

Abstract

Growth of the axial and appendicular skeleton depends on endochondral ossification, which is controlled by tightly regulated cell-cell interactions in the developing growth plates. Previous studies have uncovered an important role of a disintegrin and metalloprotease 17 (ADAM17) in the normal development of the mineralized zone of hypertrophic chondrocytes during endochondral ossification. ADAM17 regulates EGF-receptor signaling by cleaving EGFR-ligands such as TGFα from their membrane-anchored precursor. The activity of ADAM17 is controlled by two regulatory binding partners, the inactive Rhomboids 1 and 2 (iRhom1, 2), raising questions about their role in endochondral ossification. To address this question, we generated mice lacking iRhom2 (iR2-/-) with floxed alleles of iRhom1 that were specifically deleted in chondrocytes by Col2a1-Cre (iR1∆Ch). The resulting iR2-/-iR1∆Ch mice had retarded bone growth compared to iR2-/- mice, caused by a significantly expanded zone of hypertrophic mineralizing chondrocytes in the growth plate. Primary iR2-/-iR1∆Ch chondrocytes had strongly reduced shedding of TGFα and other ADAM17-dependent EGFR-ligands. The enlarged zone of mineralized hypertrophic chondrocytes in iR2-/-iR1∆Ch mice closely resembled the abnormal growth plate in A17∆Ch mice and was similar to growth plates in Tgfα-/- mice or mice with EGFR mutations. These data support a model in which iRhom1 and 2 regulate bone growth by controlling the ADAM17/TGFα/EGFR signaling axis during endochondral ossification.

Keywords: ADAM17; a disintegrin and metalloprotease 17; endochondral ossification; iRhom1, 2; inactive Rhomboid 1, 2.

MeSH terms

  • ADAM17 Protein / genetics*
  • ADAM17 Protein / metabolism
  • Animals
  • Calcification, Physiologic / genetics
  • Carrier Proteins / genetics*
  • Carrier Proteins / metabolism
  • Cell Communication
  • Cell Differentiation
  • Cell Proliferation
  • Chondrocytes / cytology
  • Chondrocytes / metabolism*
  • Chondrogenesis / genetics*
  • Collagen Type II / genetics
  • Collagen Type II / metabolism
  • ErbB Receptors / genetics
  • ErbB Receptors / metabolism
  • Gene Expression Regulation
  • Growth Plate / growth & development
  • Growth Plate / metabolism
  • Integrases / genetics
  • Integrases / metabolism
  • Membrane Proteins / deficiency
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Knockout
  • Osteogenesis / genetics*
  • Signal Transduction
  • Transforming Growth Factor alpha / genetics
  • Transforming Growth Factor alpha / metabolism

Substances

  • Carrier Proteins
  • Col2a1 protein, mouse
  • Collagen Type II
  • Membrane Proteins
  • Transforming Growth Factor alpha
  • iRhom1 protein, mouse
  • iRhom2 protein, mouse
  • EGFR protein, mouse
  • ErbB Receptors
  • Cre recombinase
  • Integrases
  • ADAM17 Protein
  • Adam17 protein, mouse