Yedgar S, Reisfeld-Granot N, Sela B A
Lipids. 1986 Oct;21(10):629-33. doi: 10.1007/BF02537211.
The viscosity of plasma and extracellular fluid has been shown to be a regulator of lipoprotein production both in cultured hepatocytes and in vivo. The possibility that this extracellular effect on cell function involves modulation of cell surface membrane components was examined. In the present work, we studied the effect of medium viscosity on liver cell gangliosides known to be involved in various membrane functions and to be located predominantly at the cell surface membrane. Cultivation of isolated hepatocytes as primary cultures markedly reduced the ganglioside content, but this reduction process was attenuated by increasing the viscosity of the culture medium. Elevation of extracellular fluid viscosity inhibited the degradation of the cell gangliosides and secretion of lysosomal enzymes involved in ganglioside degradation. The cellular activity of these enzymes as well as the activity of enzymes involved in ganglioside synthesis, CMP-NANA:GM1 sialyltransferase, CMP-NANAP:GM3 sialyltransferase and UDP-galactose:GD2 galactosyltransferase, were not affected by modulation of the extracellular medium viscosity. It is proposed that the modulation of cell ganglioside content by extracellular fluid viscosity is due to an effect on enzymes involved in ganglioside catabolism.
血浆和细胞外液的黏度已被证明在体外培养的肝细胞和体内都是脂蛋白生成的调节因子。我们研究了这种细胞外对细胞功能的影响是否涉及细胞表面膜成分的调节。在本研究中,我们研究了培养基黏度对已知参与各种膜功能且主要位于细胞表面膜的肝细胞神经节苷脂的影响。将分离的肝细胞作为原代培养物进行培养会显著降低神经节苷脂含量,但通过增加培养基的黏度可减弱这种降低过程。细胞外液黏度的升高抑制了细胞神经节苷脂的降解以及参与神经节苷脂降解的溶酶体酶的分泌。这些酶的细胞活性以及参与神经节苷脂合成的酶,即CMP-NANA:GM1唾液酸转移酶、CMP-NANAP:GM3唾液酸转移酶和UDP-半乳糖:GD2半乳糖基转移酶的活性,不受细胞外培养基黏度调节的影响。我们认为,细胞外液黏度对细胞神经节苷脂含量的调节是由于对参与神经节苷脂分解代谢的酶产生了影响。