TY - JOUR
T1 - Stimulation of cells derived from nifedipine-induced gingival overgrowth with porphyromonas gingivalis, lipopolysaccharide, and interleukin-1β
AU - Lu, H. K.
AU - Chou, H. P.
AU - Li, C. L.
AU - Wang, M. Y.
AU - Wang, Leng-Fang
PY - 2007/11
Y1 - 2007/11
N2 - The purpose of this study was to clarify the main contributory factor of nifedipine-induced gingival overgrowth either by Porphyromonas gingivalis lipopolysaccharide (Pg-LPS) or interleukin-1 beta (IL-1β). Human gingival fibroblasts from healthy tissues and nifedipine-induced gingival overgrowth tissues were stimulated with nifedipine, IL-1β Escherichia coli lipopolysaccharide (Ec-LPS), and Pg-LPS, and the gene expressions were analyzed by RT-PCR. Analysis of the data showed no strong evidence of a synergistic effect of nifedipine and Pg-LPS on IL-6, connective tissue growth factor (CTGF), and type 1 collagen gene expression of either healthy cells or nifedipine-induced gingival overgrowth cells. Among the three stimulants - IL-1β, Pg-LPS, and Ec-LPS - androgen receptor and IL-6 gene expressions in both the healthy and nifedipine-induced gingival overgrowth groups were strongly up-regulated by the presence of IL-1β only. Furthermore, the responses to IL-1β in the nifedipine-induced gingival overgrowth group were stronger than those of the healthy group. It can be concluded that IL-1β is an important mediator responsible for the higher IL-6 and androgen receptor expression of nifedipine-induced gingival overgrowth cells.
AB - The purpose of this study was to clarify the main contributory factor of nifedipine-induced gingival overgrowth either by Porphyromonas gingivalis lipopolysaccharide (Pg-LPS) or interleukin-1 beta (IL-1β). Human gingival fibroblasts from healthy tissues and nifedipine-induced gingival overgrowth tissues were stimulated with nifedipine, IL-1β Escherichia coli lipopolysaccharide (Ec-LPS), and Pg-LPS, and the gene expressions were analyzed by RT-PCR. Analysis of the data showed no strong evidence of a synergistic effect of nifedipine and Pg-LPS on IL-6, connective tissue growth factor (CTGF), and type 1 collagen gene expression of either healthy cells or nifedipine-induced gingival overgrowth cells. Among the three stimulants - IL-1β, Pg-LPS, and Ec-LPS - androgen receptor and IL-6 gene expressions in both the healthy and nifedipine-induced gingival overgrowth groups were strongly up-regulated by the presence of IL-1β only. Furthermore, the responses to IL-1β in the nifedipine-induced gingival overgrowth group were stronger than those of the healthy group. It can be concluded that IL-1β is an important mediator responsible for the higher IL-6 and androgen receptor expression of nifedipine-induced gingival overgrowth cells.
KW - Androgen receptor
KW - IL-1β
KW - IL-6
KW - Nifedipine-induced gingival over-growth
KW - Porphyromonas gingivalis
UR - http://www.scopus.com/inward/record.url?scp=36549041112&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=36549041112&partnerID=8YFLogxK
U2 - 10.1177/154405910708601115
DO - 10.1177/154405910708601115
M3 - Article
C2 - 17959904
AN - SCOPUS:36549041112
SN - 0022-0345
VL - 86
SP - 1100
EP - 1104
JO - Journal of Dental Research
JF - Journal of Dental Research
IS - 11
ER -