Literature DB >> 2997171

Hepatic retinol metabolism. Distribution of retinoids, enzymes, and binding proteins in isolated rat liver cells.

R Blomhoff, M Rasmussen, A Nilsson, K R Norum, T Berg, W S Blaner, M Kato, J R Mertz, D S Goodman, U Eriksson.   

Abstract

The main retinoids and some binding proteins and enzymes involved in retinol metabolism have been quantified in different types of rat liver cells. Hepatic perisinusoidal stellate cells contained 28-34 nmol of retinoids/10(6) cells, and parenchymal liver cells contained 0.5-0.8 nmol of retinoids/10(6) cells, suggesting that as much as 80% of more of total liver retinoids might be stored in stellate cells with the rest stored in parenchymal cells. Isolated endothelial cells and Kupffer cells contained very low levels of retinoids. More than 98% of the retinoids recovered in stellate cells were retinyl esters. Isolated parenchymal and stellate cell preparations both contained considerable retinyl palmitate hydrolase and acyl-CoA:retinol acyltransferase activities. Parenchymal cells accounted for about 75-80% of the total hepatic content of these two enzyme activities, with the rest located in stellate cells. On a cell protein basis, the concentrations of both of these activities were much greater in stellate cells than in parenchymal cells. In contrast, cholesteryl oleate and triolein hydrolase activities were fairly evenly distributed in all types of liver cells. Large amounts of cellular retinol binding proteins were also found in parenchymal and stellate cells. Although parenchymal cells accounted for more than 90% of hepatic cellular retinol binding protein, the concentration of the protein in stellate cells (per unit protein) was 22 X greater than that in parenchymal cells. Stellate cells were also enriched in cellular retinoic acid binding protein. Thus, both parenchymal and stellate cells contain substantial amounts of retinoids and of the enzymes and intracellular binding proteins involved in retinol metabolism. Stellate cells are particularly enriched in these several components.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 2997171

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  36 in total

Review 1.  Hepatic stellate cells and innate immunity in alcoholic liver disease.

Authors:  Yang-Gun Suh; Won-Il Jeong
Journal:  World J Gastroenterol       Date:  2011-05-28       Impact factor: 5.742

2.  Cellular retinyl esters and retinol among parenchymal and stellate cells in normal rat liver.

Authors:  M R Lakshman; P R Sundaresan; L L Chambers; P K Shoff
Journal:  Lipids       Date:  1988-02       Impact factor: 1.880

3.  Transfer of retinol from parenchymal to stellate cells in liver is mediated by retinol-binding protein.

Authors:  R Blomhoff; T Berg; K R Norum
Journal:  Proc Natl Acad Sci U S A       Date:  1988-05       Impact factor: 11.205

4.  Inhibition of purified pig and human liver retinyl ester hydrolase by pharmacologic agents.

Authors:  R Schindler
Journal:  Lipids       Date:  2001-05       Impact factor: 1.880

5.  Hepatic stellate cells are an important cellular site for β-carotene conversion to retinoid.

Authors:  Igor Shmarakov; Matthew K Fleshman; Diana N D'Ambrosio; Roseann Piantedosi; Ken M Riedl; Steven J Schwartz; Robert W Curley; Johannes von Lintig; Lewis P Rubin; Earl H Harrison; William S Blaner
Journal:  Arch Biochem Biophys       Date:  2010-05-12       Impact factor: 4.013

6.  Bringing retinoid metabolism into the 21st century.

Authors:  Theo J C van Berkel
Journal:  J Lipid Res       Date:  2009-09-25       Impact factor: 5.922

7.  Homeostasis of retinol in lecithin: retinol acyltransferase gene knockout mice fed a high retinol diet.

Authors:  Limin Liu; Xiao-Han Tang; Lorraine J Gudas
Journal:  Biochem Pharmacol       Date:  2008-03-27       Impact factor: 5.858

8.  Oral carcinogenesis induced by 4-nitroquinoline 1-oxide in lecithin:retinol acyltransferase gene knockout mice.

Authors:  Limin Liu; Xiao-Han Tang; Theresa Scognamiglio; Lorraine J Gudas
Journal:  J Nutr Biochem       Date:  2009-12-01       Impact factor: 6.048

Review 9.  Vitamin A signaling and homeostasis in obesity, diabetes, and metabolic disorders.

Authors:  William S Blaner
Journal:  Pharmacol Ther       Date:  2019-01-29       Impact factor: 12.310

Review 10.  PNPLA3 genetic variation in alcoholic steatosis and liver disease progression.

Authors:  Felix Stickel; Jochen Hampe; Eric Trépo; Christian Datz; Stefano Romeo
Journal:  Hepatobiliary Surg Nutr       Date:  2015-06       Impact factor: 7.293

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.