Nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and ne
urotrophin-3 (NT-3) are three representative neurotrophins responsible for
the differentiation and survival of neurons, and their high-affinity recept
ors are tropomyosin-receptor-kinase (TRK)A, TRKB, and TRKC, respectively. I
n this study, we investigated the expression of neurotrophins in a mouse pe
riodontal ligament cell line (MPL), by reverse transcription-polymerase cha
in-reaction (RT-PCR) and enzyme-linked immunoabsorbent assay (ELISA). We al
so studied the expression of TRK receptors on MPL by immunostaining and the
effects of neurotrophins on the proliferation of MPL, with a hypothesis of
autocrine mechanism of neurotrophins. Each neurotrophin and TRK receptor w
as expressed, and neurotrophins enhanced the proliferation of MPL. These fi
ndings suggest that the MPL has functional neurotrophin receptors involved
in an autocrine function of neurotrophins. The expression level of neurotro
phins and TRKs showed the reverse pattern, and we propose an auto-regulator
y mechanism of ligands and receptors in accordance with the level of synthe
sized neurotrophins.