| Literature DB >> 31990039 |
Giacomina Brunetti1, Giuseppina Storlino2, Angela Oranger2, Graziana Colaianni2, Maria F Faienza3, Giuseppe Ingravallo4, Mariasevera Di Comite1, Janne E Reseland5, Monica Celi6, Umberto Tarantino6, Giovanni Passeri7, Carl F Ware8, Maria Grano2, Silvia Colucci1.
Abstract
Bone loss induced by ovariectomy is due to the direct activity on bone cells and mesenchymal cells and to the dysregulated activity of bone marrow cells, including immune cells and stromal cells, but the underlying mechanisms are not completely known. Here, we demonstrate that ovariectomy induces the T-cell co-stimulatory cytokine LIGHT, which stimulates both osteoblastogenesis and osteoclastogenesis by modulating osteoclastogenic cytokine expression, including TNF, osteoprotegerin, and the receptor activator of nuclear factor-κB ligand (RANKL). Predictably, LIGHT-deficient (Tnfsf14-/- ) mice are protected from ovariectomy-dependent bone loss, whereas trabecular bone mass increases in mice deficient in both LIGHT and T and B lymphocytes (Rag -/- Tnfsf14 -/- ) and is associated with an inversion of the TNF and RANKL/OPG ratio. Furthermore, women with postmenopausal osteoporosis display high levels of LIGHT in circulating T cells and monocytes. Taken together, these results indicate that LIGHT mediates bone loss induced by ovariectomy, suggesting that patients with postmenopausal osteoporosis may benefit from LIGHT antagonism.Entities:
Keywords: LIGHT/TNFSF14; RANKL/OPG; TNF; bone loss; immune cells; osteoblasts; osteoclasts; osteoimmunology; ovariectomy; postmenopausal osteoporosis
Year: 2020 PMID: 31990039 DOI: 10.1002/path.5385
Source DB: PubMed Journal: J Pathol ISSN: 0022-3417 Impact factor: 7.996