Pregled bibliografske jedinice broj: 1192823
Heterotopic ossification vs. fracture healing: Extracellular vesicle cargo proteins shed new light on bone formation
Heterotopic ossification vs. fracture healing: Extracellular vesicle cargo proteins shed new light on bone formation // Bone reports, 16 (2022), 101177, 7 doi:10.1016/j.bonr.2022.101177 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1192823 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Heterotopic ossification vs. fracture healing: Extracellular vesicle cargo proteins shed new light on bone formation
Autori
Hrkač, Stela ; Novak, Ruđer ; Salai, Grgur ; Grazio, Simeon ; Vlahović, Tomislav ; Grgurević, Lovorka
Izvornik
Bone reports (2352-1872) 16
(2022);
101177, 7
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
extracellular vesicles ; Microvesicles ; Fibrodysplasia ossificans progressiva ; Myositis ossificans ; Heterotopic ossification ; Bone fractures ; Ephrin B signaling
Sažetak
Fibrodysplasia ossificans progressiva (FOP) is an extremely rare disease in which bone tissue forms in extraskeletal sites, which is known as heterotopic ossification (HO). Extracellular vesicles (EVs) are small phospholipid-enclosed particles released by various cells which have an emerging, but not completely understood role in various (patho)physiological processes. In order to further study the pathophysiology of FOP we conducted a small observational study comparing the proteomic profiles of EV cargo, derived from pooled plasma of four patient groups: FOP patient (N = 1) during active disease phase (flare-up), FOP patients during remission (N = 2), patients after long bone fracture (N = 20) and healthy controls (N = 10). After isolation of EVs – their protein cargo was determined using liquid chromatography / mass spectrometry, after which a functional gene enrichment analysis was performed. Our results show a sizeable difference of the proteomics profiles in which EVs from the bone fracture group show significant activity of integrin interactions, Wnt, VEGF, IGF-1 and PDGF pathways ; conversely, FOP patients' EVs indicate that HO occurs via processes of innate immunity and the Ephrin B signaling pathway. We hypothesize that the Ephrin B signaling (expressed in EVs) contributes to HO by aiding in mesenchymal stem cell recruitment and osteogenic differentiation, as well as by contributing to the inflammatory response, including macrophage chemotaxis and activation. This is, to our knowledge, the first published analysis of EV protein cargo in FOP.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
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)
Ustanove:
Medicinski fakultet, Zagreb,
KBC "Sestre Milosrdnice",
Klinički bolnički centar Zagreb
Profili:
Tomislav Vlahović
(autor)
Ruđer Novak
(autor)
Stela Hrkač
(autor)
Simeon Grazio
(autor)
Grgur Salai
(autor)
Lovorka Grgurević
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Emerging Sources Citation Index (ESCI)
- Scopus