Kitamura Noriko, Kaminuma Osamu, Kobayashi Noriaki, Mori Akio
National Hospital Organization, Sagamihara National Hospital, Clinical Research Center for Allergy and Rheumatology, Sagamihara, Japan.
Int Arch Allergy Immunol. 2008;146 Suppl 1:36-9. doi: 10.1159/000126059. Epub 2008 May 27.
To further understand the mechanisms of airway obstruction in asthma, it is crucial to investigate contractile responses of human airway smooth muscle. An in vitro assay system employing collagen gels embedded with well-established bronchial smooth muscle cells of human origin was explored in the present study.
Commercially available cultured human bronchial smooth muscle cells were embedded into a collagen gel. Well-known constrictors, histamine and methacholine, were added to the gel. The gel images were captured by an image analyzer, and contractile responses were evaluated.
Histamine and methacholine induced contraction of the gels in a dose-dependent manner. Pyrilamine, an H1 receptor antagonist, inhibited gel contraction in an agonist-specific manner.
Our contraction assay system, employing widely distributed cultured cells, was highly reproducible and precise. It may go a long way toward understanding mechanisms of asthmatic responses and evaluation of antiasthma drugs.
为了进一步了解哮喘气道阻塞的机制,研究人气道平滑肌的收缩反应至关重要。本研究探索了一种体外测定系统,该系统采用嵌入了成熟的人源支气管平滑肌细胞的胶原凝胶。
将市售培养的人支气管平滑肌细胞嵌入胶原凝胶中。向凝胶中加入知名的收缩剂组胺和乙酰甲胆碱。通过图像分析仪捕获凝胶图像,并评估收缩反应。
组胺和乙酰甲胆碱以剂量依赖性方式诱导凝胶收缩。H1受体拮抗剂吡苄明以激动剂特异性方式抑制凝胶收缩。
我们采用广泛分布的培养细胞的收缩测定系统具有高度的可重复性和精确性。它可能对理解哮喘反应机制和评估抗哮喘药物有很大帮助。