Pregled bibliografske jedinice broj: 1235442
Bone morphogenetic protein 3 negatively regulates bone tissue formation and regeneration
Bone morphogenetic protein 3 negatively regulates bone tissue formation and regeneration // 13th BMP Conference Book of Abstracts
Dubrovnik, Hrvatska, 2022. str. 146-146 (poster, nije recenziran, sažetak, znanstveni)
CROSBI ID: 1235442 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Bone morphogenetic protein 3 negatively regulates bone
tissue formation and regeneration
Autori
Rumenovic, Viktorija ; Vukicevic, Slobodan ; Erjavec, Igor
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
13th BMP Conference Book of Abstracts
/ - , 2022, 146-146
Skup
13th BMP Conference 2022
Mjesto i datum
Dubrovnik, Hrvatska, 08.10.2022. - 12.10.2022
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
BMP3, osteogenesis, ectopic ossification, tibial fractures, osteoprogenitors, flow cytometry
Sažetak
Introduction: Bone morphogenetic protein 3 is the most abundant BMP in bone tissue, but its role is considered antagonistic to other members of the BMP protein family. Due to the limited research of BMP3, the exact mechanism on bone formation and maintenance is not sufficiently explored. With the use of Bmp3-/- mice, this research aims to explore the effect of BMP3 on bone formation in ectopic ossification assay and regeneration of long bone fracture, as well as characterize osteoblast progenitor markers in bone marrow mesenchymal stem cells (BMSC). Methods: BMSCs were isolated from murine long bones and osteoprogenitor lineage was analyzed using flow cytometry. To assess de novo bone formation, whole blood coagulum containing BMP6 was implanted in axillary region of WT and Bmp3-/- mice of both sexes. New bone formation was assessed using micro- CT, immunohistochemistry and gene expression analysis. To evaluate bone regeneration, a model of closed tibia fracture with intramedullary pin was established and analyzed using micro-CT and Goldner staining. Results: Flow cytometry revealed an increase in early osteoprogenitor cells in Bmp3-/- mice. Ectopically formed bone showed increased bone volume fraction in both Bmp3-/- males and females, compared to WT littermates. A prevalent bone phenotype was found in Bmp3-/- mice ectopic bone, with increased expression of Runx2 and a reduced expression of Sox9, as opposed to more chondrogenic phenotype in WT mice ectopic bone. A 3-fold increase in bone callus volume during tibial fracture healing was observed in Bmp3-/- males after 21 days. Conclusion: BMP3 is shown to have an effect on early osteoprogenitor cells and its deficiency results in a higher level of new bone generation and a greater callus formation during fracture repair, thus augmenting the regulating effect of BMP3 on bone tissue growth and regeneration.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti, Interdisciplinarne društvene znanosti
POVEZANOST RADA
Projekti:
--KK.01.1.1.01.0008 - Znanstveni centar izvrsnosti za reproduktivnu i regenerativnu medicinu – istraživanja novih platormi i potencijala (CERRM) (Ježek, Davor; Vukičević, Slobodan) ( CroRIS)
--IP-2020-02-5960 - Utjecaj koštanog morfogenetskog proteina 3 (BMP3) na regeneraciju kosti (BON3gen) (Erjavec, Igor) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb