Pregled bibliografske jedinice broj: 831884
Chemokines and their receptors on osteoclast progenitor cells are involved in pathogenesis in rheumatoid arthritis
Chemokines and their receptors on osteoclast progenitor cells are involved in pathogenesis in rheumatoid arthritis // Abstract book - ECI 2015 / Bohle, Barbara (ur.).
London : Delhi: European Congress of Immunology, 2015. str. 114-114 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 831884 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Chemokines and their receptors on osteoclast progenitor cells are involved in pathogenesis in rheumatoid arthritis
Autori
Šućur, Alan ; Jajić, Zrinka ; Artuković, Marinko ; Stipić Marković, Asija ; Ivčević, Sanja ; Flegar, Darja ; Kelava, Tomislav ; Katavić, Vedran ; Kovačić, Nataša ; Grčević, Danka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Abstract book - ECI 2015
/ Bohle, Barbara - London : Delhi : European Congress of Immunology, 2015, 114-114
Skup
4th European Congress of Immunology
Mjesto i datum
Beč, Austrija, 06.09.2015. - 09.09.2015
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
osteoclast progenitors ; chemokines ; rheumatoid arthritis
Sažetak
Introduction: Joint destruction in rheumatoid arthritis (RA) involves infiltration and activation of osteoclasts. Human osteoclast progenitors (OCPs) exhibit chemotaxis and synovial compartment in RA expresses different chemokines. We aimed to define chemotactic signals by analyzing expression of chemokine receptors on OCPs, chemokine levels and to assess differentiation potential of OCPs. Materials and methods: Mononuclear cells were separated from peripheral blood of healthy controls and RA patients. Phenotype of OCPs (CD3-CD19-CD56- CD11b+CD14+) was determined using flow cytometry for following chemokine receptors: CCR1, CCR2, CCR4, CXCR4. Chemokine ligand concentrations (CCL2, CCL3, CCL4, CCL5, CXCL9, CXCL10) were measured in serum and synovial fluid using flow cytometry bead based array. OCPs were sorted and cultured with M-CSF and RANKL. After two weeks, cells were stained for TRAP enzyme and positive, mature, osteoclasts were counted. Results: Human peripheral blood OCPs similarly expressed chemokine receptors CCR1, CCR2, CCR4 and CXCR4 in RA and healthy subjects. However, CCL2, CXCL9 and CXCL10 serum levels were higher in RA, while CCL4 and CXCL10 concentrations were significantly higher in synovial fluid compared to RA serum levels. Cell culture revealed no significant differences between RA and control group. Conclusions: Although differentiation potential and receptor expression of RA OCPs is similar to control, levels of several chemokines are upregulated, indicating a possible chemotactic mechanism of OCP migration to affected joints specifically associated with RA. In parallel, we are determining the cell population responsible for increased chemokine production, most probably of the monocyte/macrophage lineage, which is induced in RA by chronic inflammation.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb
Profili:
Zrinka Jajić
(autor)
Danka Grčević
(autor)
Alan Šućur
(autor)
Tomislav Kelava
(autor)
Nataša Kovačić
(autor)
Sanja Ivčević
(autor)
Vedran Katavić
(autor)
Asja Stipić Marković
(autor)