Role of iRhoms 1 and 2 in Endochondral Ossification
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 develo...
| Main Authors: | , , , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2020-11-01
|
| Series: | International Journal of Molecular Sciences |
| Subjects: | |
| Online Access: | https://www.mdpi.com/1422-0067/21/22/8732 |
| Summary: | 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 (<i>iR2−/−</i>) with floxed alleles of iRhom1 that were specifically deleted in chondrocytes by Col2a1-Cre (<i>iR1∆Ch</i>). The resulting <i>iR2−/−iR1∆Ch</i> mice had retarded bone growth compared to <i>iR2−/−</i> mice, caused by a significantly expanded zone of hypertrophic mineralizing chondrocytes in the growth plate. Primary <i>iR2−/−iR1∆Ch</i> chondrocytes had strongly reduced shedding of TGFα and other ADAM17-dependent EGFR-ligands. The enlarged zone of mineralized hypertrophic chondrocytes in <i>iR2−/−iR1∆Ch</i> mice closely resembled the abnormal growth plate in <i>A17∆Ch</i> mice and was similar to growth plates in <i>Tgfα−/−</i> 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. |
|---|---|
| ISSN: | 1661-6596 1422-0067 |