Chinese Journal of Tissue Engineering Research ›› 2012, Vol. 16 ›› Issue (7): 1145-1149.doi: 10.3969/j.issn.1673-8225.2012.07.002

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Human osteoblasts co-cultured with bone tissue and enzymatic digestion method in vitro

Chen Jie1, Lan You-yu1, He Cheng-song1, Zhao Yi2, Liu Yi2   

  1. 1Department of Rheumatology and Hematology, the Affiliated Hospital of Luzhou Medical College, Luzhou  646000, Sichuan Province, China; 2Department of Rheumatology and Immunology, West China Hospital of Sichuan University, Chengdu  610041, Sichuan Province, China
  • Received:2011-07-05 Revised:2011-11-03 Online:2012-02-12 Published:2012-02-12
  • Contact: Liu Yi, Doctor, Professor, Department of Rheumatology and Immunology, West China Hospital of Sichuan University, Chengdu 610041, Sichuan Province, China i2006liu@163.com
  • About author:Chen Jie★, Master, Attending physician, Department of Rheumatology and Hematology, the Affiliated Hospital of Luzhou Medical College, Luzhou 646000, Sichuan Province, China cjlion@qq.com

Abstract:

BACKGROUND: It is difficult to culture osteoblasts, and different in cell number, purity, proliferation and differentiation activity obtained by different culture methods.
OBJECTIVE: To investigate the ideal culturing method of the human osteoblasts in vitro. 
METHODS: Human osteoblasts were isolated from trabecular bone of ilium by bone tissue and enzymatic digestion methods.
RESULTS AND CONCLUSION: The isolated and cultured human osteoblasts were in good condition and had a high purity. The cells were adherent growth, diversification in morphology, and mostly showed polygonal, spindle-shaped, triangular, and the cytoplasm was abundant and the spurt was stretched out. It has the typical characteristics of osteoblasts. The cells proliferation was well, alkaline phosphatase staining and mineralized nodules alizarin red staining was positive. We successfully cultured osteoblasts in vitro from trabecular bone of ilium by bone tissue and enzymatic digestion methods; it indicated that was the ideal method to culture osteoblasts.

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