Baraniuk J N, Wong G, Ali M, Sabol M, Troost T
Division of Rheumatology, Immunology and Allergy, Georgetown University, Washington, DC 20007-2197, USA.
Thorax. 1998 Jul;53(7):577-82. doi: 10.1136/thx.53.7.577.
Activated c-fos binds to jun proteins to form the activation protein 1 (AP-1) transcription factor that regulates cytokine and other proinflammatory genes. c-Fos may play a key role in nasal polyp formation. Glucocorticoids may exert their anti-inflammatory effects through an interaction of glucocorticoid receptors with AP-1 that leads to mutual inactivation of both factors, and a "default" termination of AP-1 mediated gene activation. This may explain the beneficial effects of glucocorticoids in the treatment of nasal polyps.
To test this hypothesis in humans in vivo the immunohistochemical expression of c-fos-immunoreactive material (c-fos-irm) was assessed in nasal polyps from eight steroid naive subjects, polyps from eight subjects treated with topical beclomethasone dipropionate (BDP), and normal inferior turbinate nasal mucosa (n = 6).
mRNA for c-fos was detected in all nasal polyps and normal mucosa. In contrast, c-fos-irm was present in all steroid naive subjects but in only two of the eight subjects treated with BDP (p = 0.007, two-tailed Fisher's exact test). c-Fos-irm was expressed solely in epithelial cells and glandular structures; it was expressed in normal epithelium and glands, but the staining intensity was low.
Glucocorticoids appear to modulate expression of c-fos-irm and possibly AP-1 in human airway epithelial cells in vivo.
活化的c-fos与jun蛋白结合形成活化蛋白1(AP-1)转录因子,该转录因子可调节细胞因子及其他促炎基因。c-Fos可能在鼻息肉形成中起关键作用。糖皮质激素可能通过糖皮质激素受体与AP-1相互作用发挥抗炎作用,这种相互作用导致两个因子相互失活,并使AP-1介导的基因激活“默认”终止。这可能解释了糖皮质激素在鼻息肉治疗中的有益作用。
为了在人体体内验证这一假设,对8名未使用过类固醇的受试者的鼻息肉、8名使用丙酸倍氯米松(BDP)局部治疗的受试者的鼻息肉以及正常下鼻甲鼻黏膜(n = 6)进行免疫组织化学检测,评估c-fos免疫反应性物质(c-fos-irm)的表达。
在所有鼻息肉和正常黏膜中均检测到c-fos的mRNA。相比之下,c-fos-irm在所有未使用过类固醇的受试者中均有表达,但在8名使用BDP治疗的受试者中只有2名有表达(p = 0.007,双侧Fisher精确检验)。c-Fos-irm仅在上皮细胞和腺结构中表达;在正常上皮和腺体中也有表达,但染色强度较低。
糖皮质激素似乎在体内调节人气道上皮细胞中c-fos-irm的表达,可能还调节AP-1的表达。