H-3-thymidine incorporation was studied in cultured human nasal and articul
ar chondrocytes exposed to low-energy, low-frequency pulsed electromagnetic
fields (PEMFs) (75 Hz, 2.3 mT). The reverse transcriptase polymerase chain
reaction (RT-PCR) analysis shows that human secondary chandrocytes derived
from both nasal and articular cartilage express collagen type TI mRNA, whi
ch is a specific marker of the chondrocyte phenotype. In a preliminary seri
es of experiments, cells were exposed to PEMF for different time periods ra
nging from 6 to 30 hours (timecourse), in medium supplemented with 10% or 0
.5% fetal calf serum (FCS) and in serum-free medium. The ratios between the
H-3-thymidine incorporation in PEMFs and control cultures Show an increase
of the cell proliferation in cultures exposed to PEMFs when serum is prese
nt in the culture medium, whereas no effect was observed in serum-free cond
itions. The increase in DNA synthesis, induced by PEMFs, was then evaluated
only at the times of maximum induction and the results were analyzed by th
e three-factor analysis of variance (ANOVA).
The data presented in this study show that even if H-3-thymidine incorporat
ion is higher in nasal than in articular chondrocytes, PEMF induce an incre
ase in the proliferation of both cell types. Moreover, the concentration of
FCS in the culture medium greatly influences the proliferative response of
human chondrocytes to the PEMF exposure. Though normal human osteoblast ce
lls increase their proliferation when exposed to PEMFs if only 10% FCS is p
resent in the medium, human chondrocytes are able to increase their cell pr
oliferation when exposed to PEMFs in the presence of both 0.5% and 10% of F
CS in the medium. The results obtained may help to explain the basic mechan
isms of PEMF stimulation of fracture healing.