Patel Hema J, Belvisi Maria G, Bishop-Bailey David, Yacoub Magdi H, Mitchell Jane A
Respiratory Pharmacology Group, Department of Cardiothoracic Surgery, Faculty of Medicine, The National Heart and Lung Institute, Imperial College School of Medicine, London, United Kingdom.
J Immunol. 2003 Mar 1;170(5):2663-9. doi: 10.4049/jimmunol.170.5.2663.
Airway smooth muscle is actively involved in the inflammatory process in diseases such as chronic obstructive pulmonary disease and asthma by 1) contributing to airway narrowing through hyperplasia and hypertrophy and 2) the release of GM-CSF and G-CSF, which promotes the survival and activation of infiltrating leukocytes. Thus, the identification of novel anti-inflammatory pathways in airway smooth muscle will have important implications for the treatment of inflammatory airway disease. This study identifies such a pathway in the activation of peroxisome proliferator-activated receptors (PPARs). PPAR ligands are known therapeutic agents in the treatment of diabetes; however, their role in human airway disease is unknown. We demonstrate, for the first time, that human airway smooth muscle cells express PPAR alpha and -gamma subtypes. Activation of PPAR gamma by natural and synthetic ligands inhibits serum-induced cell growth more effectively than does the steroid dexamethasone, and induces apoptosis. Moreover, PPAR gamma activation, like dexamethasone, inhibits the release of GM-CSF. However, PPAR gamma ligands, but not dexamethasone, similarly inhibits G-CSF release. These results reveal a novel anti-inflammatory pathway in human airway smooth muscle, where PPAR gamma activation has additional anti-inflammatory effects to those of steroids. Hence, PPAR ligands might act as potential treatments in human respiratory diseases.
1)通过增生和肥大导致气道狭窄;2)释放粒细胞巨噬细胞集落刺激因子(GM-CSF)和粒细胞集落刺激因子(G-CSF),从而促进浸润白细胞的存活和活化。因此,鉴定气道平滑肌中新型抗炎途径对炎症性气道疾病的治疗具有重要意义。本研究在过氧化物酶体增殖物激活受体(PPARs)的激活过程中鉴定出了这样一条途径。PPAR配体是治疗糖尿病的已知治疗药物;然而,它们在人类气道疾病中的作用尚不清楚。我们首次证明,人类气道平滑肌细胞表达PPARα和γ亚型。天然和合成配体激活PPARγ比类固醇地塞米松更有效地抑制血清诱导的细胞生长,并诱导细胞凋亡。此外,与地塞米松一样,PPARγ激活可抑制GM-CSF的释放。然而,PPARγ配体而非地塞米松同样抑制G-CSF的释放。这些结果揭示了人类气道平滑肌中的一种新型抗炎途径,其中PPARγ激活具有比类固醇更多的抗炎作用。因此,PPAR配体可能成为人类呼吸系统疾病的潜在治疗方法。