Sato K, Tomura H, Igarashi Y, Ui M, Okajima F
Laboratory of Signal Transduction, Gunma University, Maebashi, Japan. kosato@news sb.gunma-u.ac.jp
Biochem Biophys Res Commun. 1997 Nov 17;240(2):329-34. doi: 10.1006/bbrc.1997.7666.
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.
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。