Pregled bibliografske jedinice broj: 1187647
Pdgfrβ Signaling inhibits BMP2-Mediated Osteogenesis in Bone Healing
Pdgfrβ Signaling inhibits BMP2-Mediated Osteogenesis in Bone Healing // Orthopaedic Research Society (ORS) 2022 Annual Meeting
Tampa (FL), Sjedinjene Američke Države, 2022. 1, 1 (poster, međunarodna recenzija, neobjavljeni rad, znanstveni)
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Naslov
Pdgfrβ Signaling inhibits BMP2-Mediated
Osteogenesis in Bone Healing
Autori
Novak, Sanja ; Shum, Laura ; Madunić, Josip ; Vučetic, Milan ; Wang, Xi ; Kalajzić, Ivo
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, neobjavljeni rad, znanstveni
Skup
Orthopaedic Research Society (ORS) 2022 Annual Meeting
Mjesto i datum
Tampa (FL), Sjedinjene Američke Države, 04.02.2022. - 08.02.2022
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
bone defect ; bone morphogenetic protein 2 ; Platelet derived growth factor ; osteogenesis
Sažetak
Bone regeneration depends on a pool of bone/cartilage progenitor cells and mechanisms regulating differentiation. We aimed to evaluate the in vivo effects of PDGF and BMP2 signaling using bone healing models. Targeted deletion of PDGFRb in aSMA osteoprogenitors led to increased callus density and bone mass, resulting in improved biomechanical properties. To evaluate critical size bone defects, we utilized aSMACreER crossed with Ai9 reporter as a marker of osteoprogenitor cells (SMA9) and Col2.3GFP to identify mature osteoblast lineage cells. BMP2 treatment increased proportion of αSMA9+ progenitor cells, which were decreased when PDGF BB was combined with BMP2. BMP2 induced significant bone formation and a number of Col2.3GFP+ osteoblasts, which were decreased with PDGF BB. This is the first in vivo study showing inhibition of BMP2-induced osteogenesis by PDGF signaling. Controlling PDGF signaling during osteogenesis might lead to better treatment options during bone regeneration.
Izvorni jezik
Engleski
Znanstvena područja
Biologija