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首页> 外文期刊>Journal of receptor and signal transduction research >Specific stimulation of migration of human keratinocytes by mu-opiate receptor agonists
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Specific stimulation of migration of human keratinocytes by mu-opiate receptor agonists

机译:阿片受体激动剂对人角质形成细胞迁移的特异性刺激

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摘要

There are several indications that neuropeptides, especially the opiate receptor agonists, modulate the immune response by stimulating the formation of granulation tissue and enhancing the reepithelialization. We observed that the mu-opiate receptor ligand beta-endorphin stimulates the migration of cultured human foreskin keratinocytes. After I hour exposure to 1 muM beta-endorphin, the keratinocytes experienced an increase of cell diameter by cellular elongation and stimulation of migration. Dynorphin had a lesser effect under the same condition. The opiate receptor antagonist naltrexone significantly reduced the effect of beta-endorphin on keratinocyte migration. This migratory effect of mu-opiate receptor agonists in vitro indicates that the opioid peptides, released in wounds, could play a key role in the final reepithelialization and tissue regeneration in wound healing. This new knowledge will help us not only to understand the mechanism of wound healing but also to improve the therapeutic strategy in the healing of painful chronic wounds. [References: 18]
机译:有多种迹象表明,神经肽,尤其是阿片受体激动剂,通过刺激肉芽组织的形成并增强再上皮形成来调节免疫反应。我们观察到,阿片受体配体β-内啡肽可刺激培养的人包皮角质形成细胞的迁移。在暴露于1μMβ-内啡肽的1小时后,角质形成细胞通过细胞伸长和迁移迁移而经历了细胞直径的增加。强啡肽在相同条件下的作用较小。阿片受体拮抗剂纳曲酮显着降低了β-内啡肽对角质形成细胞迁移的影响。穆阿片受体激动剂在体外的这种迁移作用表明,释放在伤口中的阿片样物质肽可能在伤口愈合的最终再上皮化和组织再生中起关键作用。这一新知识将不仅帮助我们了解伤口愈合的机制,而且还将改善慢性疼痛伤口愈合的治疗策略。 [参考:18]

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