- Author:
Guo-Ye MO
1
;
Shun-Cong ZHANG
1
;
Yong-Xian LI
1
;
Hui-Zhi GUO
1
;
Dan-Qing GUO
1
;
Da-Xing LI
1
;
Yong-Chao TANG
1
;
Ling MO
2
,
3
;
Pei-Jie LUO
1
;
Yan-Huai MA
1
Author Information
- Publication Type:Journal Article
- Keywords: Gene expression; Osteoblast; Osteoclast
- MeSH: 3T3 Cells; Animals; Cell Differentiation; Coculture Techniques; Mice; NF-kappa B; metabolism; Osteoblasts; cytology; Osteoclasts; cytology; Osteoprotegerin; metabolism; RANK Ligand; metabolism; RAW 264.7 Cells; Receptor Activator of Nuclear Factor-kappa B; metabolism; Transforming Growth Factor beta1; metabolism
- From: China Journal of Orthopaedics and Traumatology 2018;31(3):241-247
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo establish osteoblast-osteoclast cell co-culture system in a Transwell chamber, and detect cell viability of osteoblasts and osteoclasts in system.
METHODSOsteoblast MC3T3-E1 and mouse monocytes RAW264.7 were cultivated in vitro. RANKL-induced mouse RAW264.7 monocytes differentiated into mature osteoclasts, osteoblast-osteoclast cell co-culture system was established in Transwell chamber. Cell activity of osteoblasts and osteoclasts were detected by CCK-8 experimenting, Alizarin Red staining, TRAP staining. The expression of OPG, ALP, RANKL, TGF-b1 gene and RANKL protein in osteoblast MC3T3-E1 were detected by PCR, Western-Blot methods. Also, the expression of RANK, NF-κB in gene and protein level in osteoclast were measured through the same method respectively.
RESULTSThe co-culture system of Mouse MC3T3-E1 cells and RAW264.7 cell were established in Transwell chamber. Co-culture system affected cell division activities of osteoblasts and osteoclasts. Differentiation of osteoblasts were increased, while differentiation of osteoclast division were slight decreased under microscope observation. OPG (0.65±0.08) and ALP (0.16±0.01) gene expression of co-culture system were less than single culture OPG(1.00±0.08) and ALP (1.01±0.16); TGF-b1(4.42±0.21) and RANKL(4.12±1.04) of osteoblasts in co-culture system were higher than TGF-b1(1.00±0.10) and RANKL(1.00±0.09) under single culture. However, gene expression of RANK(0.63±0.06) and NF-κB(0.64±0.08) in co-culture system were decreased than RANK(1.00±0.08) and NF-κB(1.00±0.09), in single culture, and had significant differences. Similarly, protein expression of OPG(0.43±0.05) and NF-κB(0.59±0.05) of co-culture system were less than OPG(0.84±0.06) and NF-κB(1.13±0.03) of single culture. While RANKL protein expression (0.54±0.03)of co-culture system was more than single culture RANKL(0.31±0.03), and had statistically differences, which was in agreement of the trend of gene expression change.
CONCLUSIONSCo-culture system of mouse MC3T3-E1 cells and RAW264.7 cell was viable in Transwell chamber, and the activity of osteoblasts is higher than osteoclasts in co-culture system.