Expression of receptors of Vitamin D and cytokines in osteoclasts differentiated by M-CSF and ODF.
10.5051/jkape.2002.32.4.865
- Author:
Soo Mi SEONG
1
;
Heung Sik UM
;
Sung Hee KO
;
Kyung Mi WOO
;
Beom Seok CHANG
Author Information
1. Department of Periodontology, College of Dentistry, Kangnung National University, Korea.
- Publication Type:Original Article
- Keywords:
Macrophage Colony-Stimulating Factor;
Oseoclast Differentiatiion Factor;
Osteoclast;
Vit D;
Cytokine
- MeSH:
Animals;
Bone Marrow Cells;
Collagenases;
Cytokines*;
Digestion;
Dihydroergotamine;
DNA, Complementary;
Edetic Acid;
Femur;
Humans;
Humerus;
Interleukin-1;
Macrophage Colony-Stimulating Factor*;
Mice;
Needles;
Osteoclasts*;
Periodontal Diseases;
Polymerase Chain Reaction;
Radius;
RANK Ligand;
Receptors, Calcitriol;
RNA;
RNA-Directed DNA Polymerase;
Tibia;
Tooth Loss;
Trypsin;
Vitamin D*;
Vitamins*
- From:The Journal of the Korean Academy of Periodontology
2002;32(4):865-873
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
The primary cause of tooth loss after 30 years of age is periodontal disease. Destruction of alveolar bone by periodontal disease is done by bone resorbing activity of osteoclasts. Understanding differentiation and activation mechanism of osteoclasts is essential for controling periodontal disease. The purpose of this study is to identify the possible effects of Vitamin D and cytokines affecting osteoclasts and its precursor cells. Four to six week-old mice were killed and humerus, radius, tibia and femur were removed aseptically and washed two times with Hank's solution containing penicillin-streptomycin and then soft tissue were removed. Bone marrow cells were collected by 22 gauge needle. Cells were cultured in Hank's solution containing 1 mg/ml type II collagenase, 0.05% trypsin, 4mM EDTA. Supernatant solution was removed 5 times after 15 minutes of digestion with above mentioned enzyme solution, and remained bone particles were maintained in alpha-MEM for 15 minutes and 4degrees C temperature. Bone particles were agitated for 1 minute and supernatant solution containing osteoclast precursor cells were filtrated with cell stainer. These separated osteoclast precursor cells were dispensed with 100-mm culture dish by 1x10(7) cells unit and cultured in alpha-MEM containing 20 ng/ml recombinant human M-CSF, 30 ng/ml recombinant human soluble osteoclast differentiation factor and 10% fetal calf serum for 2 and 7 days. Total RNA of osteoclast precursor cells were extracted using RNeasy kit. One microgram of total RNA was reverse transcribed in 42degrees C for 30 minutes using SuperScriptII reverse transcriptase. Expression of transcribed receptors of each hormone and cytokine were traced with 1 microliter of cDNA solution by PCR amplification. Vitamin D receptor was found in cells cultured for 7 days. TNF-alphareceptor was found in cells cultured for 2 days and amount of receptors were increased by 7 days. IL-1 type I receptor was not found in cells cultured 2 and 7 days. But, IL-1 receptor type II was found in cells cultured for 2 days. TGF-alpha,betatype I receptor was found in cells cultured 2 and 7 days, and amount of receptors were increased by 7 days of culture. These results implies Vitamin D and cytokines can affect osteoclasts directly, and affecting period in differentiation cycle of osteoclasts is different by Vitamin D and cytokines.
