Pregled bibliografske jedinice broj: 527525
Keratocan is Expressed by Osteoblasts and Can Modulate Osteogenic Differentiation
Keratocan is Expressed by Osteoblasts and Can Modulate Osteogenic Differentiation // Connective tissue research, 52 (2011), 5; 401-407 doi:10.3109/03008207.2010.546536 (međunarodna recenzija, članak, znanstveni)
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Naslov
Keratocan is Expressed by Osteoblasts and Can Modulate Osteogenic Differentiation
Autori
Igwe, John C. ; Gao, Qi ; Kizivat, Tomislav ; Kao, Winston W. ; Kalajzić, Ivo
Izvornik
Connective tissue research (0300-8207) 52
(2011), 5;
401-407
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
keratocan; osteoblast; osteocyte; differentiation
Sažetak
Keratocan is an extracellular matrix protein that belongs to the small leucine-rich proteoglycan family that also includes lumican, biglycan, decorin, mimecan, and fibromodulin. Members of this family are known to play a role in regulating cellular processes such as proliferation and modulation of osteoprogenitor lineage differentiation. The aims of this study were to evaluate the expression pattern of the keratocan within the osteoprogenitor lineage and to assess its role in regulating osteoblast maturation and function. Results from gene expression analyses of cells at different maturation stages within the osteoblast lineage indicate that keratocan is differentially expressed by osteoblasts and shows little or no expression by osteocytes. During primary osteoblast cultures, high keratocan mRNA expression was observed on day 14, whereas lower expression was detected at days 7 and 21. To assess the effects of keratocan on osteoprogenitor cell differentiation, we evaluated primary calvarial cell cultures from keratocan-deficient mice. The mineralization of calvarial osteoblast cultures derived from keratocan null (Kera–/–) mice was lower than in wild-type osteoblast cultures. Furthermore, analysis of RNA derived from Kera−/− calvarial cell cultures showed a reduction in the mature osteoblast differentiation markers, that is, bone sialoprotein and osteocalcin. In addition, we have evaluated the bone formation in keratocan-deficient mice. Histomorphometric analysis indicated that homozygous knockout mice have significantly decreased rates of bone formation and mineral apposition. Taken together, our results demonstrate the expression of keratocan by osteoblast lineage cells and its ability to modulate osteoblast function.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
219-2192190-2186 - Prevencija stvaranja i recidiva mokraćnih kamenca (Tucak, Antun, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Osijek
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
Uključenost u ostale bibliografske baze podataka::
- Calcium and Calcified Tissue Abstracts
- Academic Search Complete
- BIOBASE
- Biological Abstracts
- Biochemistry and Biophysics Citation Index
- Biomedical Reference Collection: Comprehensive
- Chemical Abstracts
- Chemical Hazards in Industry
- Chemical Safety Newsbase
- EMBASE
- EMBIOLOGY
- ETOH
- IBZ
- IBR
- Journal Citation Reports/Science Edition
- Laboratory Hazards Bul