Expression and function of the P2X7 receptor in human osteoblasts: The role of NFATc1 transcription factor.
Leticia Scussel BergaminLetizia PenolazziElisabetta LambertiniSimonetta FalzoniAlba Clara SartiCaroline M MolleFernand-Pierre GendronPasquale De BonisFrancesco Di VirgilioRoberta PivaPublished in: Journal of cellular physiology (2020)
Bone mineralization is an orchestrated process by which mineral crystals are deposited by osteoblasts; however, the detailed mechanisms remain to be elucidated. The presence of P2X7 receptor (P2X7R) in immature and mature bone cells is well established, but contrasting evidence on its role in osteogenic differentiation and deposition of calcified bone matrix remains. To clarify these controversies in the present study, we investigated P2X7R participation in bone maturation. We demonstrated that the P2X7R is expressed and functional in human primary osteoblasts, and identified in the P2RX7 promoter several binding sites for transcription factors involved in bone mineralization. Of particular interest was the finding that P2X7R expression is enhanced by nuclear factor of activated T cells cytoplasmic 1 (NFATc1) overexpression, and accordingly, NFATc1 is recruited at the P2RX7 gene promoter in SaOS2 osteoblastic-like cells. In conclusion, our data provide further insights into the regulation of P2X7R expression and support the development of drugs targeting this receptor for the therapy of bone diseases.
Keyphrases
- transcription factor
- bone mineral density
- poor prognosis
- bone loss
- soft tissue
- nuclear factor
- endothelial cells
- bone regeneration
- dna methylation
- gene expression
- toll like receptor
- postmenopausal women
- bone marrow
- induced apoptosis
- cell proliferation
- inflammatory response
- genome wide
- body composition
- machine learning
- electronic health record
- vascular smooth muscle cells
- high resolution