Nakamura M, Nishida T, Ofuji K, Reid T W, Mannis M J, Murphy C J
Department of Ophthalmology, Yamaguchi University School of Medicine, Ube City, Yamaguchi, Japan.
Exp Eye Res. 1997 Sep;65(3):321-9. doi: 10.1006/exer.1997.0345.
In order to investigate the role of neural regulation in corneal epithelial healing, we examined the effect of substance P (SP) on corneal epithelial migration using an organ culture system of rabbit corneas. We investigated the synergistic effects of SP with (1) growth factors: epidermal growth factor (EGF), basic fibroblast growth factor (bFGF), and transforming growth factor-beta(TGF-beta); (2) extracellular matrix proteins: fibronectin, vitronectin, laminin, and collagen type IV; and (3) cytokines: interleukin-1alpha (IL-1alpha), IL-1beta, and interleukin-6 (IL-6). Rabbit corneal blocks were cultured in the absence or presence of various reagents for 24 hr. The corneal blocks were then fixed, dehydrated, embedded in paraffin and stained by hematoxylin-eosin, and the length of the path of epithelial migration was measured. The addition of SP alone, at concentrations up to 50 microg ml-1, did not affect epithelial migration. EGF, fibronectin, vitronectin, collagen type IV, and IL-6 stimulated epithelial migration, but bFGF, TGF-beta, laminin, IL-1alpha, and IL-1betadid not. The stimulatory effect of EGF on the epithelial migration was enhanced by the presence of SP. This synergistic effect of SP and EGF on corneal epithelial migration was abolished by the addition of an SP antagonist or enkephalinase. Other neurotransmitters (vasoactive intestinal peptide, calcitonin gene-related peptide, acetylcholine chloride, norepinephrine, serotonin) and tachykinins (neurokinin A, neurokinin B, kassinin, eledoisin, physalaemin) were examined, but none exhibited a synergistic effect with EGF. Interestingly, EGF alone stimulated the incorporation of 3H-thymidine into corneal epithelial cells, but the addition of SP with EGF did not enhance this effect. These results demonstrate that SP enhanced the EGF stimulation of corneal epithelial migration in vitro in a specific manner, suggesting a possible role of SP as a modulator of epithelial wound healing.
为了研究神经调节在角膜上皮愈合中的作用,我们使用兔角膜器官培养系统,检测了P物质(SP)对角膜上皮迁移的影响。我们研究了SP与以下物质的协同作用:(1)生长因子:表皮生长因子(EGF)、碱性成纤维细胞生长因子(bFGF)和转化生长因子-β(TGF-β);(2)细胞外基质蛋白:纤连蛋白、玻连蛋白、层粘连蛋白和IV型胶原;(3)细胞因子:白细胞介素-1α(IL-1α)、IL-1β和白细胞介素-6(IL-6)。兔角膜块在无或有各种试剂的情况下培养24小时。然后将角膜块固定、脱水、石蜡包埋并用苏木精-伊红染色,测量上皮迁移路径的长度。单独添加浓度高达50μg/ml的SP不影响上皮迁移。EGF、纤连蛋白、玻连蛋白、IV型胶原和IL-6刺激上皮迁移,但bFGF、TGF-β、层粘连蛋白、IL-1α和IL-1β则无此作用。SP的存在增强了EGF对上皮迁移的刺激作用。添加SP拮抗剂或脑啡肽酶可消除SP和EGF对角膜上皮迁移的这种协同作用。还检测了其他神经递质(血管活性肠肽、降钙素基因相关肽、氯化乙酰胆碱、去甲肾上腺素、5-羟色胺)和速激肽(神经激肽A、神经激肽B、蛙皮素、eledoisin、physalaemin),但均未显示与EGF有协同作用。有趣的是,单独的EGF刺激角膜上皮细胞掺入3H-胸腺嘧啶,但SP与EGF一起添加并未增强此作用。这些结果表明,SP以特定方式增强了EGF在体外对角膜上皮迁移的刺激作用,提示SP可能作为上皮伤口愈合的调节剂发挥作用。