Pregled bibliografske jedinice broj: 549668
Decreased plating efficiency, proliferation and osteogenic differentiation of synovial fluid mesenchymal progenitors as a marker of severity of juvenile idiopathic arthritis
Decreased plating efficiency, proliferation and osteogenic differentiation of synovial fluid mesenchymal progenitors as a marker of severity of juvenile idiopathic arthritis // Arthritis Research & Therapy: 1st Bio-Rheumatology International Congress (BRIC2011)
London : Delhi: BioMed Central, 2011. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 549668 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Decreased plating efficiency, proliferation and osteogenic differentiation of synovial fluid mesenchymal progenitors as a marker of severity of juvenile idiopathic arthritis
Autori
Lazić Mosler, Elvira ; Jelušić-Dražić, Marija ; Grčević, Danka ; Marušić, Ana ; Kovačić, Nataša
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Arthritis Research & Therapy: 1st Bio-Rheumatology International Congress (BRIC2011)
/ - London : Delhi : BioMed Central, 2011
Skup
1st Bio-Rheumatology International Congress (BRIC2011)
Mjesto i datum
Tokyo, Japan, 14.11.2011. - 16.11.2011
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
juvenile idiopathic arthritis; osteoblasts; synovial fibroblasts
Sažetak
Background Juvenile idiopathic arthritis (JIA) is a rheumatic pediatric disease characterized by synovial inflammation in one or more joints [1]. Inflammation results in hyperplastic changes of the synovium, destruction of articular cartilage and subchondral osteoresorption. Murine models of arthritis revealed impaired osteogenic/chondrogenic differentiation of synovial mesenchymal progenitors via inflammation-induced activation of NF-κB [2]. We aimed to explore frequency, plating efficiency and osteoblastogenic potential of synovial mesenchymal progenitors and correlate them with intensity of local and systemic inflammation in patients with JIA. Materials and methods Synovial fluid cells were collected from 19 patients with oligoarticular JIA (oJIA) and 8 patients with poliarticular JIA (pJIA), plated in density 1.5×106/mL in 24-well plates, and cultured in αMEM + 10% FCS. Osteoblastogenesis was stimulated by the addition of 50 μg/ml ascorbic acid and 5 mmol β-glycerophosphate. To exclude inflammatory and hematopoietic cells, adherent cells were passaged three times, and osteoblastogenesis again induced in fourth passage (P4). Osteoblastogenesis was assessed by intensity of alkaline phospatase (AP) histochemical staining. In addition, osteoblast (Runx2, AP, OPG, RANKL) and cytokine/chemokine (IL-1, IL-4, CCL2, CCL4 and MIP1α) gene expression were assessed in P4 osteoblastogenic cultures. Results Plating efficiency of synovial mesenchymal progenitors was decreased in patients with pJIA in comparison to patients with oJIA. Passage was successful only in 3 (37.5%) pJIA patients, and 18 (94.7%) oJIA patients. Plated at equal density, P4 synovial adherent cells from pJIA patients formed less fibroblastic colonies. Osteoblastogenesis was higher in children with oJIA than in children with pJIA, both from primary synovial cells (median 1119.08 ; IQR 476.57-1470.26 vs. 141.58 ; IQR 14.47-237.50, arbitrary units, p<0.005, Mann-Whitney test), and P4 cells (median 1162.00 ; IQR 102.00 to 5484.50 vs. 12.00 ; IQR 6.00-307.37, arbitrary units, p<0.05). Osteoblastogenesis from primary synoviocytes negatively correlated with erythrocyte sedimentation rate (ρ= –0.4139, p=0.03), and synovial concentration of IL-17 (ρ= –0.4174, p=0.04). Expression of osteoprotegerin and CCL2 was decreased in P4 osteoblastogenic cultures from pJIA in comparison with oJIA patients (p<0.05). Conclusions Severe forms of JIA are characterized by decreased proliferation, osteogenic differentiation and immunoregulatory potential of synovial mesenchymal cells, correlating with inflammatory activity.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
108-1080229-0142 - Molekularni mehanizmi učinaka imunosnih poremećaja na kost (Grčević, Danka, MZOS ) ( CroRIS)
108-1080229-0140 - Molekularne interakcije koštanog i imunološkog sustava (Marušić, Ana, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb
Profili:
Nataša Kovačić
(autor)
Elvira Lazić Mosler
(autor)
Danka Grčević
(autor)
Ana Marušić
(autor)
Marija Jelušić
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- Scopus
- MEDLINE