Suppr超能文献

外源性1-磷酸鞘氨醇可能通过PC12细胞表面的一种受体诱导神经突回缩。

Exogenous sphingosine 1-phosphate induces neurite retraction possibly through a cell surface receptor in PC12 cells.

作者信息

Sato K, Tomura H, Igarashi Y, Ui M, Okajima F

机构信息

Laboratory of Signal Transduction, Gunma University, Maebashi, Japan. kosato@news sb.gunma-u.ac.jp

出版信息

Biochem Biophys Res Commun. 1997 Nov 17;240(2):329-34. doi: 10.1006/bbrc.1997.7666.

Abstract

Exogenous sphingosine 1-phosphate (S1P), like lysophosphatidic acid (LPA), induced neurite retraction or cell rounding in differentiated PC12 cells. The lysosphingolipid-induced shape change was detected at as low as 1 nM; however, a significant accumulation of intracellular S1P was not detected until 1 microM S1P was applied. Moreover, although exogenous sphingosine caused a significant increase in intracellular S1P by sphingosine kinase-catalyzed phosphorylation, the effect on the shape change was marginal. Exposure of the cells to the immobilized S1P in which the lipid was covalently linked to a glass carrier also resulted in the shape change. These results suggest that the exogenous S1P-induced shape change does not require uptake of the lipid into the cells but possibly requires interaction with a cell surface receptor in the neuronal cells.

摘要

外源性1 -磷酸鞘氨醇(S1P)与溶血磷脂酸(LPA)一样,可诱导分化的PC12细胞发生神经突回缩或细胞变圆。溶血鞘脂诱导的形态变化在低至1 nM时即可检测到;然而,直到施加1 μM S1P时才检测到细胞内S1P的显著积累。此外,尽管外源性鞘氨醇通过鞘氨醇激酶催化的磷酸化导致细胞内S1P显著增加,但其对形态变化的影响很小。将细胞暴露于脂质与玻璃载体共价连接的固定化S1P中也会导致形态变化。这些结果表明,外源性S1P诱导的形态变化不需要脂质进入细胞,但可能需要与神经元细胞表面受体相互作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验