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izvor podataka: crosbi

Immature osteoblast lineage cells increase osteoclastogenesis in osteogenesis imperfecta murine (CROSBI ID 152496)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Li, Haitao ; Jiang, Xi ; Delaney, John ; Franceschetti, Tiziana ; Bilić-Curčić, Ines ; Kalinovsky, Judy ; Lorenzo, Joseph ; Grčević, Danka ; Rowe, David W ; Kalajzić, Ivo Immature osteoblast lineage cells increase osteoclastogenesis in osteogenesis imperfecta murine // American journal of pathology, 14 (2010), 10; 1121-1134

Podaci o odgovornosti

Li, Haitao ; Jiang, Xi ; Delaney, John ; Franceschetti, Tiziana ; Bilić-Curčić, Ines ; Kalinovsky, Judy ; Lorenzo, Joseph ; Grčević, Danka ; Rowe, David W ; Kalajzić, Ivo

engleski

Immature osteoblast lineage cells increase osteoclastogenesis in osteogenesis imperfecta murine

This study addressed the role of impairment of osteoblastic differentiation as a mechanism underlying pathophysiology of the osteogenesis imperfecta (OI). We hypothesize that combination of impaired osteogenic differentiation with increased bone resorption leads to diminished bone mass. By introducing visual markers of distinct stages of osteoblast differentiation ; pOBCol3.6GFP (3.6GFP ; preosteoblast) and pOBCol2.3GFP (2.3GFP ; osteoblast/osteocytes) into the OIM model, we assessed osteoblast maturation and the mechanism of increased osteoclastogenesis. Cultures from oim/oim ; 2.3GFP mice showed a marked reduction of cells expressing GFP relative to +/+ ; 2.3GFP littermates. No significant difference in expression of 3.6GFP between the +/+ and oim/oim mice was observed. Histological analysis of the oim/oim ; 3.6GFP mice showed an increased area of GFP positive cells lining the endocortical surface compared to +/+ ; 3.6GFP mice. In contrast GFP expression was similar between oim/oim ; 2.3GFP and +/+ ; 2.3GFP mice. These data indicate that the lineage is under continuous stimulation, while only a proportion of cells attain the mature osteoblast stage. The immature osteoblasts exhibit a stronger potential to support osteoclast formation and differentiation. We detected a higher Rankl/Opg ratio and higher expression of Tnf-alpha in sorted immature osteoblasts. In addition, increased osteoclast formation was observed when osteoclast progenitors were co-cultured with oim/oim derived osteoblasts compared with osteoblasts derived from +/+ mice. Our data indicates that osteoblast lineage maturation is a critical aspect underlying the pathophysiology of OI.

osteoblasts; osteoclasts; osteogenesis imperfecta

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Podaci o izdanju

14 (10)

2010.

1121-1134

objavljeno

0002-9440

Povezanost rada

Temeljne medicinske znanosti

Indeksiranost