results show that bile acids strongly interfere with the The existence of a relationship between bile acid and assembly or secretion of VLDL particles by human hepatriacylglycerol metabolism in humans has been estabtocytes, suggesting a physiological function of the enlished, but the underlying mech
Regulation of low density lipoprotein receptor activity in primary cultures of human hepatocytes by serum lipoproteins
โ Scribed by Louis M. Havekes; Hans Verboom; Elly de Wit; Sing Hiem Yap; Hans M. G. Princen
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 634 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0270-9139
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The responsiveness of low density lipoprotein (LDL) binding and uptake was measured in a human hepatoblastoma cell line, Hep G2. These cells exhibited both saturable, high-affinity and nonsaturable low-affinity components similar to that described for LDL binding in other mammalian cells. In additio
Low density lipoprotein (LDL) processing was investigated in a human hepatoma-derived cell line, Hep G2. Hep G2 cells bound, internalized and degraded LDL via a saturable, high affinity (Kd -2 x lo-' M ) pathway similar to that present in other mammalian cells. Although 80% of the uptake and degrada
Low density lipoprotein (LDL) processing was investigated in a human hepatoma-derived cell line, Hep G2. Hep G2 cells bound, internalized and degraded LDL via a saturable, high affinity (Kd -2 x lo-' M ) pathway similar to that present in other mammalian cells. Although 80% of the uptake and degrada
Hepatocellular heterogeneity of biochemical function is well established for many aspects of liver metabolism. This study addresses the question of cellular heterogeneity in the catabolism of low-density lipoprotein by rat hepatocytes. Low-density lipoprotein binding (4" C) and uptake (37" C) by rat
We found that the binding of lzS1-low-density lipoprotein to fetal liver low-density lipoprotein receptor rose progressively with the increase in fetal age. During this period, total cholesterol and low-density lipoprotein-cholesterol levels in fetal serum declined significantly. The correlation coe