ba0003pp405 | Other diseases of bone and mineral metabolism | ECTS2014
Cappariello Alfredo
, Paone Riccardo
, Capulli Mattia
, Rucci Nadia
, Muraca Maurizio
, Teti Anna
In autosomal recessive osteopetrosis due to mutations of the TNFSF11 gene, deficiency of the pro-osteoclastogenic cytokine RANKL prevents osteoclast formation. RANKL is a membrane-bound protein cleaved into active soluble (s)RANKL by various enzymes, including metalloproteinase 14 (MMP14). We created a bio-device that released sRANKL and induced osteoclastogenesis in tnfsf11−/− mice. We tested various RANKL cell sources, and used mouse primary calvarial osteoblasts...