Department of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy.
FEBS Lett. 2013 Jul 11;587(14):2199-204. doi: 10.1016/j.febslet.2013.05.042. Epub 2013 May 24.
The modulation of the HDL receptor scavenger receptor B1 (SRB1) was evaluated in skin fibroblasts isolated from patients with Rett syndrome (RTT), a genetic form of infantile autism. Patients showed an altered plasma lipid profile, while their skin fibroblasts showed a dramatic reduction in SRB1 (immunogold, Western blot and immunohistochemistry). The decreased SRB1 levels were demonstrated to be the consequence of its binding with 4-hydroxy-2-nonenal (4HNE), a product of lipid peroxidation, and its increased ubiquitination. Our findings show for the first time a loss of SRB1 in RTT cells and its relationship with a chronic oxidative stress status.
我们评估了瑞特综合征(RTT)患者皮肤成纤维细胞中高密度脂蛋白受体清道夫受体 B1(SRB1)的调节情况。RTT 是一种遗传性婴儿自闭症。患者表现出改变的血浆脂质谱,而他们的皮肤成纤维细胞显示出 SRB1 的显著减少(免疫金、Western blot 和免疫组织化学)。减少的 SRB1 水平被证明是其与脂质过氧化产物 4-羟基-2-壬烯醛(4HNE)结合及其增加的泛素化的结果。我们的研究结果首次表明 RTT 细胞中 SRB1 的丢失及其与慢性氧化应激状态的关系。