Copyright
©2010 Baishideng Publishing Group Co.
World J Gastroenterol. Dec 21, 2010; 16(47): 5946-5952
Published online Dec 21, 2010. doi: 10.3748/wjg.v16.i47.5946
Published online Dec 21, 2010. doi: 10.3748/wjg.v16.i47.5946
Figure 1 Biliary and non-biliary fecal cholesterol excretion.
In this proposed model, cholesterol is effluxed from peripheral cells onto high-density lipoprotein (HDL) and then delivered to the liver or small intestine via HDL or very low density lipoprotein (VLDL)/low-density lipoprotein (LDL) following cholesterol ester transfer protein-mediated transfer. The cholesterol internalized or de novo synthesized by the liver is secreted into bile through the action of ABCG5/G8 and subsequently excreted in the feces. Alternatively, the liver secretes the cholesterol in apoB-containing lipoproteins or HDL containing apoAI or apoE, which are specifically targeted to the small intestine. After being internalized by scavenger receptor, class B, type I (SR-BI), LDL receptor (LDLR), or another lipoprotein receptor system, the cholesterol is trafficked across the enterocytes to the brush border membrane and effluxed into the intestinal lumen by ABCG5/G8 or a currently unidentified cholesterol transporter.
- Citation: Temel RE, Brown JM. A new framework for reverse cholesterol transport: Non-biliary contributions to reverse cholesterol transport. World J Gastroenterol 2010; 16(47): 5946-5952
- URL: https://www.wjgnet.com/1007-9327/full/v16/i47/5946.htm
- DOI: https://dx.doi.org/10.3748/wjg.v16.i47.5946