The Hajdu Cheney mutation sensitizes mice to the osteolytic actions of tumor necrosis factor ?.

ABSTRACT: Hajdu Cheney syndrome (HCS) is characterized by craniofacial developmental abnormalities, acro-osteolysis, and osteoporosis and is associated with gain-of-NOTCH2 function mutations. A mouse model of HCS termed Notch2tm1.1Ecan harboring a mutation in exon 34 of Notch2 replicating the one found in HCS was used to determine whether the HCS mutation sensitizes the skeleton to the osteolytic effects of tumor necrosis factor ? (TNF?). TNF? injected over the calvarial vault caused a greater increase in osteoclast number, osteoclast surface, and eroded surface in Notch2tm1.1Ecan mice compared with littermate WT controls. Accordingly, the effect of TNF? on osteoclastogenesis was greatly enhanced in cultures of bone marrow-derived macrophages (BMMs) from Notch2tm1.1Ecan mice when compared with the activity of TNF? in control cultures. TNF? induced the expression of Notch2 and Notch2 mutant mRNA by ?2-fold, possibly amplifying the NOTCH2-dependent induction of osteoclastogenesis. The effect of TNF? on osteoclastogenesis in Notch2tm1.1Ecan mutants depended on NOTCH2 activation because it was reversed by anti-NOTCH2 negative regulatory region and anti-jagged 1 antibodies. The inactivation of Hes1 prevented the TNF? effect on osteoclastogenesis in the context of the Notch2tm1.1Ecan mutation. In addition, the induction of Il1b, but not of Tnfa and Il6, mRNA by TNF? was greater in Notch2tm1.1Ecan BMMs than in control cells, possibly contributing to the actions of TNF? and NOTCH2 on osteoclastogenesis. In conclusion, the HCS mutation enhances TNF?-induced osteoclastogenesis and the inflammatory bone-resorptive response possibly explaining the acro-osteolysis observed in affected individuals.

SUBMITTER: Yu J 

PROVIDER: S-EPMC6768656 | biostudies-literature | 2019 Sep

REPOSITORIES: biostudies-literature