Pregled bibliografske jedinice broj: 408250
Osteocytes can Modulate Osteoblastic Activity via NPY Signaling
Osteocytes can Modulate Osteoblastic Activity via NPY Signaling // Journal of Bone and Mineral Research
Montréal, Kanada, 2009. str. 144-144 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 408250 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Osteocytes can Modulate Osteoblastic Activity via NPY Signaling
Autori
Igwe, JC ; San Miguel, SM ; Paic, Frane ; Li, HT ; Kalajzic, Ivo
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Journal of Bone and Mineral Research
/ - , 2009, 144-144
Skup
30th Annual Meeting of American Society for Bone and Mineral Research
Mjesto i datum
Montréal, Kanada, 12.09.2008. - 16.09.2008
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
osteocytes; gene expression analysis
Sažetak
Osteocytes are characterized by long neuronal-like cell processes, which may actively participate in the release of molecules that modulate the function of other surrounding bone cells. The location of osteocytes and their inherent inability to divide represents a major obstacle for studying osteocyte biology. We have previously shown that dentin matrix protein 1 (DMP1) is preferentially expressed in cells embedded within the bone matrix (osteocytes) or in partially embedded cells (preosteocytes). This was the key observation leading to generation of an osteocyte-specific GFP transgenic mouse (DMP-1GFP). To investigate the expression of regulatory molecules produced by osteocytes, we utilized dual transgenic mouse in which osteocytes are idenitified by DMP-1-GFP(green), while osteoblasts are labeled by Col2.3GFP(blue). An in vivo gene expression analysis was generated by fluorescence activated sorting of neonatal calvarial cells derived from these dual transgenic mice. It was an intriguing observation that the osteocytes expressed neuropeptide Y (NPY), a gene whose role in the central control of bone mass has been well established. We confirmed this result by immunohistochemical detection of NPY in osteocytes. Furthermore, NPY mRNA expression was observed in DMP1GFP+ cells (osteocytes) and Col2.3GFP+ cells (osteoblasts/osteocytes) derived from fluorescent sorting of primary calvarial osteogenic cultures. RNA analysis of the isolated osteocytes demonstrated increased levels of NPY mRNA transcripts in both DMP1GFP+ and Col2.3GFP+ populations. In addition, we investigate the expression of NPY receptors in cultured osteoblast lineage cells. qPCR analysis of cultured calvarial osteoblasts demonstrated that mRNA of the NPY receptor subtypes Y1 and Y6 increased significantly between day 7 and day 14 of culture. We further investigated the effect of NPY at this stage of culture by in vitro treatment with NPY protein. Northern blot analysis of RNA from 1 nM NPY treated calvarial osteoblasts, showed a significant reduction of osteocalcin and bone sialoprotein expression at day 14 of culture. These results demonstrate the effect of NPY on mature osteoblasts, suggesting a novel, local regulation of osteoblast function by osteocytes via NPY signaling.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
108-1080399-0335 - Eksperimentalni embrionalni tumori i razvoj zametaka sisavaca in vitro i in vivo (Jakuš, Florijana, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE