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白细胞介素1α是内皮细胞衰老的一个标志物。

Interleukin 1 alpha is a marker of endothelial cellular senescent.

作者信息

Mariotti Massimo, Castiglioni Sara, Bernardini Daniela, Maier Jeanette A M

机构信息

Department of Preclinical Sciences, University of Milan Medical School, Via GB Grassi, 74 Milan, Italy.

出版信息

Immun Ageing. 2006 Apr 6;3:4. doi: 10.1186/1742-4933-3-4.

Abstract

BACKGROUND

The functional changes associated with endothelial senescence may be involved in human aging and age-related vascular disorders. Since the inflammatory cytokine interleukin (IL-)1 inhibits endothelial growth, we evaluated the expression of IL-1alpha, IL-1beta and their antagonist, the IL-1 receptor antagonist (IL-1ra), in endothelial in vitro senescence and quiescence. We also examined the expression of IL-1alpha in human senescent and progeric fibroblasts.

RESULTS

We found that the overexpression of IL-1alpha specifically characterizes endothelial senescence. No modulation of this cytokine was observed in endothelial quiescence and in senescent or progeric human fibroblasts. The expression of IL-1beta and IL-1ra was also assessed and found not to be affected by senescence.

CONCLUSION

Our results indicate that a dysfunction of the cytokine network associates with aging and point to a specific role of IL-1alpha in endothelial senescence.

摘要

背景

与内皮细胞衰老相关的功能变化可能参与人类衰老及与年龄相关的血管疾病。由于炎性细胞因子白细胞介素(IL-)1抑制内皮细胞生长,我们评估了IL-1α、IL-1β及其拮抗剂IL-1受体拮抗剂(IL-1ra)在内皮细胞体外衰老和静止状态下的表达。我们还检测了IL-1α在人类衰老和成早衰成纤维细胞中的表达。

结果

我们发现IL-1α的过表达是内皮细胞衰老的特异性特征。在内皮细胞静止状态以及衰老或成早衰人类成纤维细胞中未观察到该细胞因子的调节变化。我们还评估了IL-1β和IL-1ra的表达,发现其不受衰老影响。

结论

我们的结果表明细胞因子网络功能障碍与衰老相关,并指出IL-1α在内皮细胞衰老中具有特定作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92aa/1482715/7aab592f1981/1742-4933-3-4-1.jpg

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