Kawase T, Okuda K, Wu C H, Yoshie H, Hara K, Burns D M
Department of Pharmacology, Niigata University School of Dentistry, Japan.
J Periodontal Res. 1999 Apr;34(3):160-8. doi: 10.1111/j.1600-0765.1999.tb02237.x.
In many peripheral tissues, calcitonin gene-related peptide (CGRP) is released from peptidergic sensory nerve fibres and acts like a growth factor during tissue development and regeneration. However, the ability of CGRP to influence gingival tissue has not been studied. To address this question, we have now examined the effects of CGRP on the proliferation of human gingival fibroblasts (Gin-1) in vitro. Gin-1 cells have approximately 3100 specific CGRP-binding sites with a Kd of 38.6 pM on their surface. Treatment with CGRP (0.1-100 nM) significantly stimulated cell proliferation in a dose-dependent manner, with maximal effects at 1-10 nM CGRP after 2 d. As one early cellular response to CGRP, p44-MAPK protein (also known as the extracellular signal response kinase [ERK]) was tyrosine- and threonine-phosphorylated within 2 min, and this phosphorylation was sustained for at least 1 h. The dose-response curve of MAPK activation was very similar to that observed for CGRP's stimulation of cell proliferation. In addition, CGRP's activation of MAPK stimulated its ability to phosphorylate the Elk-1 transcription factor. When cells were pretreated with PD98059, a selective inhibitor of MAPK kinase (also known as MEK), CGRP not only failed to induce phosphorylation of MAPK but also failed to stimulate Gin-1 cell proliferation. Our present data indicate that CGRP rapidly activates the MAPK signalling pathway, an effect which consequently stimulates the proliferation of gingival fibroblasts. Our data demonstrate specific cellular responses to CGRP by gingival fibroblasts and support the possibility that CGRP acts as a targeted local factor in the regulation of development, generation and/or regeneration of gingival tissues.
在许多外周组织中,降钙素基因相关肽(CGRP)从肽能感觉神经纤维释放出来,并在组织发育和再生过程中发挥生长因子的作用。然而,CGRP对牙龈组织的影响尚未得到研究。为了解决这个问题,我们现在研究了CGRP对体外培养的人牙龈成纤维细胞(Gin-1)增殖的影响。Gin-1细胞表面有大约3100个特异性CGRP结合位点,解离常数(Kd)为38.6 pM。用CGRP(0.1 - 100 nM)处理能以剂量依赖的方式显著刺激细胞增殖,在2天后,1 - 10 nM CGRP时效果最佳。作为细胞对CGRP的早期反应之一,p44-MAPK蛋白(也称为细胞外信号调节激酶[ERK])在2分钟内酪氨酸和苏氨酸发生磷酸化,且这种磷酸化持续至少1小时。MAPK激活的剂量反应曲线与CGRP刺激细胞增殖所观察到的曲线非常相似。此外,CGRP对MAPK的激活增强了其磷酸化Elk-1转录因子的能力。当细胞用MAPK激酶(也称为MEK)的选择性抑制剂PD98059预处理时,CGRP不仅未能诱导MAPK磷酸化,也未能刺激Gin-1细胞增殖。我们目前的数据表明,CGRP迅速激活MAPK信号通路,这一效应进而刺激牙龈成纤维细胞的增殖。我们的数据证明了牙龈成纤维细胞对CGRP的特异性细胞反应,并支持CGRP作为调节牙龈组织发育、生成和/或再生的靶向局部因子的可能性。