Sobue G, Yamamoto M, Doyu M, Li M, Yasuda T, Mitsuma T
Department of Neurology, Nagoya University School of Medicine, Japan.
Neurochem Res. 1998 Jun;23(6):821-9. doi: 10.1023/a:1022434209787.
The steady-state mRNA levels of NGF, BDNF and NT-3, and the mRNA levels of their receptors p75NGFR, trk, trkB, and trkC were examined in various human peripheral neuropathies, to determine the correlation with myelinated fiber pathology and T cell and macrophage invasions in the diseased nerves. Steady state levels of p75NGFR mRNAs were significantly elevated in nerves with axonal pathology. In contrast, steady state levels of trkB and trkC mRNA levels were diminished. trk mRNA was not detected in the human nerves. The NGF, BDNF, and NT-3 mRNA levels were elevated in the diseased nerves. The increase in BDNF and NT-3 mRNA levels were proportional to the extent of invasion of the nerves by T cells and macrophages, but did not directly correlate with axonal nor demyelinating pathology, thus suggesting that inflammatory cell invasions are involved in the regulation of BDNF and NT-3 mRNA expressions. These neurotrophin and their receptor gene expressions in the diseased human nerves would be regulated by an underlying pathology-related process, and could play a role in peripheral nerve repair.
在各种人类周围神经病变中,检测了神经生长因子(NGF)、脑源性神经营养因子(BDNF)和神经营养因子3(NT-3)的稳态mRNA水平,以及它们的受体p75神经生长因子受体(p75NGFR)、酪氨酸激酶受体(trk)、trkB和trkC的mRNA水平,以确定其与患病神经中髓鞘纤维病理以及T细胞和巨噬细胞浸润的相关性。在有轴突病理改变的神经中,p75NGFR mRNA的稳态水平显著升高。相反,trkB和trkC mRNA水平的稳态水平降低。在人类神经中未检测到trk mRNA。患病神经中NGF、BDNF和NT-3的mRNA水平升高。BDNF和NT-3 mRNA水平的升高与T细胞和巨噬细胞对神经的浸润程度成正比,但与轴突或脱髓鞘病理改变无直接相关性,因此提示炎症细胞浸润参与了BDNF和NT-3 mRNA表达的调节。这些神经营养因子及其受体基因在患病人类神经中的表达可能受潜在的病理相关过程调控,并可能在周围神经修复中发挥作用。