| Literature DB >> 30446170 |
Hiroaki Yokomori1, Wataru Ando2, Masaya Oda3.
Abstract
Caveolins (CAVs) regulate intracellular cholesterol transport by a complex process involving caveolae, endoplasmic reticulum (ER), and the Golgi network. Hepatic stellate cells (HSCs) are the central site for retinoid storage in the liver and indeed the entire body. Herein, we attempted to elucidate the ultrastructural localization and expression of caveolin-1 (CAV-1) in human HSCs during the progression of liver cirrhosis (LC). Normal and hepatitis C-related cirrhotic liver samples were prepared using a modified perfusion-fixation method to fix organelle structures and molecules in their in vivo positions, and examined using immunoelectron microscopy. In control liver specimens, CAV-1 was minimally associated with low electron density lipid droplets (LDs) segregated around zones 1-2, and specifically associated with membranes surrounding LDs. CAV-1 was segregated in high-density LDs, consistent with the formation of membrane-enclosed lipid-rich vesicular structures, as well as caveolae on plasma membranes around zones 2-3. In cirrhotic liver specimens, CAV-1 molecules were inserted into the cytoplasmic leaflets of ER membranes for transportation to LDs. Thus, CAV-1 transport to LDs might represent an intracellular pathway from the ER in cirrhotic liver tissue.Entities:
Keywords: Caveolae; Hepatic stellate cell; Immunoelectron microscopy; Lipid droplet; Rough endoplasmic reticulum; caveolin-1
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Year: 2018 PMID: 30446170 DOI: 10.1016/j.acthis.2018.10.008
Source DB: PubMed Journal: Acta Histochem ISSN: 0065-1281 Impact factor: 2.479