Genetic Deficiency of the Long Pentraxin 3 Affects Osteogenesis and Osteoclastogenesis in Homeostatic and Inflammatory Conditions.
Valentina GranataDario StrinaMaria Lucia SchiavoneBarbara BottazziAlberto MantovaniAntonio InforzatoCristina SobacchiPublished in: International journal of molecular sciences (2023)
The long pentraxin 3 (PTX3) is a soluble glycoprotein made by immune and nonimmune cells endowed with pleiotropic functions in innate immunity, inflammation, and tissue remodeling. PTX3 has recently emerged as a mediator of bone turnover in both physiological and pathological conditions, with direct and indirect effects on osteoblasts and osteoclasts. This notwithstanding, its role in bone biology, with major regard to the osteogenic potential of osteoblasts and their interplay with osteoclasts, is at present unclear. Here, we investigated the contribution of this pentraxin to bone deposition in the osteogenic lineage by assessing collagen production, mineralization capacity, osteoblast maturation, extracellular matrix gene expression, and inflammatory mediators' production in primary osteoblasts from the calvaria of wild-type (WT) and Ptx3 -deficient ( Ptx3 -/- ) mice. Also, we evaluated the effect of PTX3 on osteoclastogenesis in cocultures of primary osteoblasts and bone marrow-derived osteoclasts. Our investigations were carried out both in physiological and inflammatory conditions to recapitulate in vitro aspects of inflammatory diseases of the bone. We found that primary osteoblasts from WT animals constitutively expressed low levels of the protein in osteogenic noninflammatory conditions, and genetic ablation of PTX3 in these cells had no major impact on collagen and hydroxyapatite deposition. However, Ptx3 -/- osteoblasts had an increased RANKL/OPG ratio and CD44 expression, which resulted in in enhanced osteoclastogenesis when cocultured with bone marrow monocytes. Inflammation (modelled through administration of tumor necrosis factor-α, TNF-α) boosted the expression and accumulation of PTX3 and inflammatory mediators in WT osteoblasts. In these conditions, Ptx3 genetic depletion was associated with reduced collagen deposition and immune modulators' production. Our study shed light on the role of PTX3 in osteoblast and osteoclast biology and identified a major effect of inflammation on the bone-related properties of this pentraxin, which might be relevant for therapeutic and/or diagnostic purposes in musculoskeletal pathology.
Keyphrases
- bone loss
- oxidative stress
- bone marrow
- bone regeneration
- bone mineral density
- mesenchymal stem cells
- induced apoptosis
- gene expression
- extracellular matrix
- wild type
- poor prognosis
- rheumatoid arthritis
- dna methylation
- postmenopausal women
- soft tissue
- genome wide
- cell cycle arrest
- type diabetes
- body composition
- metabolic syndrome
- small molecule
- copy number
- single cell
- lps induced
- signaling pathway
- tissue engineering
- climate change
- cell death
- risk assessment
- skeletal muscle
- drug induced
- atomic force microscopy
- long non coding rna
- insulin resistance
- high resolution