首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Glucocorticoids decrease tissue mast cell number by reducing the production of the c-kit ligand stem cell factor by resident cells: in vitro and in vivo evidence in murine systems.
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Glucocorticoids decrease tissue mast cell number by reducing the production of the c-kit ligand stem cell factor by resident cells: in vitro and in vivo evidence in murine systems.

机译:糖皮质激素通过减少驻留细胞产生的c-kit配体干细胞因子来减少组织肥大细胞的数量:在鼠类系统中的体外和体内证据。

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摘要

The local delivery of glucocorticoids to tissues significantly decreases mast cell number. This pharmacologic effect of glucocorticoids is believed to be one of the mechanisms by which glucocorticoids regulate allergic inflammation. To determine the mechanism by which glucocorticoids are able to exert this effect, we first applied the glucocorticoid fluocinonide to mouse dermis and observed that the decrease in mast cell number was associated with an increase in mast cell apoptosis. This did not appear to be due to a direct effect of the glucocorticoid on mast cells, as the addition of 0.01-1.0 microM of the glucocorticoid dexamethasone into stem cell factor (SCF)-dependent mast cell cultures did not enhance mast cell death. However, addition of dexamethasone to cultured fibroblasts did result in a downregulation of SCF mRNA and a significant decrease in SCF protein production. Similarly, immunohistochemistry performed on fluocinonide-treated mouse dermis revealed a decrease in immunoreactive SCF. Administration of SCF at sites of fluocinonide administration to the dermis abolished the mast cell-depleting effect of this glucocorticoid. Thus, glucocorticoids decrease tissue mast cell number by downregulating tissue SCF production required for the survival of local mast cells. This observation may be applicable to the design of improved strategies to treat mast cell-mediated disorders.
机译:糖皮质激素向组织的局部递送显着降低了肥大细胞数量。糖皮质激素的这种药理作用被认为是糖皮质激素调节过敏性炎症的机制之一。为了确定糖皮质激素能够发挥这种作用的机制,我们首先将糖皮质激素氟考尼特应用于小鼠真皮,并观察到肥大细胞数量的减少与肥大细胞凋亡的增加有关。这似乎不是由于糖皮质激素对肥大细胞的直接作用,因为向干细胞因子(SCF)依赖性肥大细胞培养物中添加0.01-1.0 microM的糖皮质激素地塞米松不会增加肥大细胞的死亡。但是,向培养的成纤维细胞中添加地塞米松确实会导致SCF mRNA的下调和SCF蛋白产量的显着下降。类似地,对氟喹诺酮治疗的小鼠真皮进行的免疫组织化学显示免疫反应性SCF降低。在对氟西诺肽施用至真皮的部位施用SCF消除了该糖皮质激素的肥大细胞消耗作用。因此,糖皮质激素通过下调局部肥大细胞存活所需的组织SCF产生来减少组织肥大细胞数量。该观察结果可能适用于设计治疗肥大细胞介导的疾病的策略。

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