Pregled bibliografske jedinice broj: 1162536
Notch 1 inhibition increases osteoclast progenitor activity in the mouse model of rheumatoid arthritis
Notch 1 inhibition increases osteoclast progenitor activity in the mouse model of rheumatoid arthritis // Annual meeting of the Croatian immunological society 2021
Trogir, Hrvatska, 2021. str. 18-18 (predavanje, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 1162536 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Notch 1 inhibition increases osteoclast progenitor
activity in the mouse model of rheumatoid arthritis
Autori
Filipović, Maša ; Šućur, Alan ; Flegar, Darja ; Jajić, Zrinka ; Ikić Matijašević, Marina ; Lukač, Nina ; Kovačić, Nataša ; Kelava, Tomislav ; Šisl, Dino ; Zrinski Petrović, Katerina ; Katavić, Vedran ; Grčević, Danka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Annual meeting of the Croatian immunological society 2021
/ - , 2021, 18-18
Skup
Annual Meeting of the Croatian Immunological Society 2021
Mjesto i datum
Trogir, Hrvatska, 23.09.2021. - 25.09.2021
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Domaća recenzija
Ključne riječi
osteoclast progenitors ; collagen-induced arthritis ; Notch ; Jagged ; Delta-like
Sažetak
Background: Osteoclast progenitor cells (OCPs) are susceptible to regulation through Notch signaling. We previously identified an increased frequency of OCPs expressing Notch receptors in arthritic mice. We aimed to determine the effects of Notch receptor signaling inhibition on OCP activity in murine collagen-induced arthritis (CIA). Methods: Periarticular bone marrow (PBM) and spleen (SPL) were harvested from mice with CIA, additionally treated by i.p. injections of anti-Notch 1 neutralizing antibodies (1mg/kg). FACS sorted OCPs were stimulated by osteoclastogenic factors (M- CSF/RANKL), in Jagged (JAG)1 or Delta-like (DLL)1 coated wells, with or without anti-Notch 1 antibodies. The research was approved by the Ethics Committee. Results: Seeding OCPs on DLL1- coated wells increased, whereas seeding on JAG1- coated wells decreased the number of TRAP+ osteoclasts and expression of osteoclast differentiation genes. Addition of anti-Notch 1 antibodies to ligand-stimulated OCPs resulted in an increased number of TRAP+ osteoclasts, partially reversing Jag1 inhibition. In vivo treatment with anti-Notch 1 antibodies did not affect total OCP frequency, but increased the expression of Notch 4 both in PBM and SPL as seen by flow cytometry. Additionally, anti-Notch 1 treatment stimulated Notch transcription factors HES and HEY. Both PBM and SPL cultured OCPs from anti-Notch 1 treated mice produced a higher number of large TRAP+ osteoclasts and exhibited increased expression of osteoclast differentiation genes. Conclusion: Both in vitro and in vivo anti-Notch 1 neutralizing antibodies enhanced osteoclastogenesis in CIA model, implying an inhibitory role of Notch 1 signaling in osteoclast differentiation.
Izvorni jezik
Engleski
POVEZANOST RADA
Projekti:
IP-2018-01-2414 - Notch signaling in osteoclast progenitors induced by rheumatoid arthritis (NORA) (Grčević, Danka, HRZZ - 2018-01) ( CroRIS)
UIP-2017-05-1965 - Uloga Notch signalnog puta u patogenezi jetrene fibroze (NOFIBRO) (Kelava, Tomislav, HRZZ - 2017-05) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb,
Klinička bolnica "Sveti Duh",
KBC "Sestre Milosrdnice"
Profili:
Zrinka Jajić
(autor)
Danka Grčević
(autor)
Alan Šućur
(autor)
Maša Filipović
(autor)
Marina Ikić Matijašević
(autor)
Dino Šisl
(autor)
Tomislav Kelava
(autor)
Nataša Kovačić
(autor)
Darja Flegar
(autor)
Vedran Katavić
(autor)
Nina Lukač
(autor)