Expression and biological roles of heat shock protein 25 in rat dental follicle cells.
- Author:
Yu DU
1
;
Jun-Qi LING
;
Hai-Jing GU
;
Qi-Mei GONG
;
Nan XIE
Author Information
- Publication Type:Journal Article
- MeSH: Alkaline Phosphatase; metabolism; Animals; Cell Proliferation; Cells, Cultured; Dental Sac; metabolism; Flow Cytometry; Fluorescent Antibody Technique, Indirect; HSP27 Heat-Shock Proteins; physiology; Immunohistochemistry; Rats; Tetrazolium Salts; Thiazoles; Up-Regulation
- From: Chinese Journal of Stomatology 2009;44(8):492-496
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo examine the expression of heat shock protein 25 (HSP-25) in dental rat follicles in vivo and in vitro in order to investigate the possible effect of HSP-25 on cell proliferation and alkaline phosphatase (ALP) activity.
METHODSThe expression of HSP-25 in mandibles of postnatal rats from day 1, 3, 5, 7, 9, 11 was examined by immunohistochemistry in vitro, the expression of HSP-25 in the dental follicle cells was detected by the indirect immunofluorescence method. Methyl thiazolyl tetrazolium (MTT) assay, flowcytometry and ALP assay were used to detect the effect of HSP-25 on rat dental follicles.
RESULTSHSP-25 expression was absent or weak in rat dental follicle cells at early postnatal stage and present from day 5 till day 11. HSP-25 was detected in the cytoplasm of cultured dental follicle cells. MTT results showed no effect could be detected on dental follicle cell proliferation after stimulation of different concentrations of HSP-25 on day 1, 2, 3. Flowcytometry results also exhibited no difference in cell cycles after stimulation of HSP-25 at 0 microg/L and 100 microg/L. HSP-25 at a concentration of 50 microg/L and 100 microg/L could up-regulate the ALP activity on day 9.
CONCLUSIONSExpression of HSP-25 increases chronologically in the rat dental follicle cells. HSP-25 locates in the cytoplasm of cultured rat dental follicle cells. HSP-25 has no effect on the proliferation of dental follicle cells, however it can up-regulate the ALP activity.