TY - JOUR
T1 - An immortalized rat liver stellate cell line (HSC-T6)
T2 - A new cell model for the study of retinoid metabolism in vitro
AU - Vogel, Silke
AU - Piantedosi, Roseann
AU - Frank, Jorge
AU - Lalazar, Avraham
AU - Rockey, Don C.
AU - Friedman, Scott L.
AU - Blaner, William S.
PY - 2000/6
Y1 - 2000/6
N2 - Hepatocytes and hepatic stellate cells play important roles in retinoid storage and metabolism. Hepatocytes process postprandial retinyl esters and are responsible for secretion of retinol bound to retinol-binding protein (RBP) to maintain plasma retinol levels. Stellate cells are the body's major cellular storage sites for retinoid. We have characterized and utilized an immortalized rat stellate cell line, HSC-T6 cells, to facilitate study of the cellular aspects of hepatic retinoid processing. For comparison, we also carried out parallel studies in Hepa-1 hepatocytes. Like activated primary stellate cells, HSC-T6 express myogenic and neural crest cytoskeletal filaments. HSC-T6 cells take up and esterify retinol in a time- and concentration-dependent manner. Supplementation of HSC-T6 culture medium with free fatty acids (up to 300 μM) does not affect retinol uptake but does enhance retinol esterification up to 10-fold. RT-PCR analysis indicates that HSC-T6 cells express all 6 retinoid nuclear receptors (RARα, -β, -γ, and RXRα, -β, -γ) and like primary stellate cells, HSC-T6 stellate cells express cellular retinol-binding protein, type I (CRBP) but fail to express either retinol-binding protein (RBP) or transthyretin (TTR). Addition of retinol (10-8-10-5 M) or all-trans-retinoic acid (10-10-10-6 M) rapidly up-regulates CRBP expression. Using RAR-specific agonists and antagonists and an RXR-specific agonist, we show that members of the RAR- receptor family modulate HSC-T6 CRBP expression. Thus, HSC-T6 cells display the same retinoid-related phenotype as primary stellate cells in culture and will be a useful tool for study of hepatic retinoid storage and metabolism.
AB - Hepatocytes and hepatic stellate cells play important roles in retinoid storage and metabolism. Hepatocytes process postprandial retinyl esters and are responsible for secretion of retinol bound to retinol-binding protein (RBP) to maintain plasma retinol levels. Stellate cells are the body's major cellular storage sites for retinoid. We have characterized and utilized an immortalized rat stellate cell line, HSC-T6 cells, to facilitate study of the cellular aspects of hepatic retinoid processing. For comparison, we also carried out parallel studies in Hepa-1 hepatocytes. Like activated primary stellate cells, HSC-T6 express myogenic and neural crest cytoskeletal filaments. HSC-T6 cells take up and esterify retinol in a time- and concentration-dependent manner. Supplementation of HSC-T6 culture medium with free fatty acids (up to 300 μM) does not affect retinol uptake but does enhance retinol esterification up to 10-fold. RT-PCR analysis indicates that HSC-T6 cells express all 6 retinoid nuclear receptors (RARα, -β, -γ, and RXRα, -β, -γ) and like primary stellate cells, HSC-T6 stellate cells express cellular retinol-binding protein, type I (CRBP) but fail to express either retinol-binding protein (RBP) or transthyretin (TTR). Addition of retinol (10-8-10-5 M) or all-trans-retinoic acid (10-10-10-6 M) rapidly up-regulates CRBP expression. Using RAR-specific agonists and antagonists and an RXR-specific agonist, we show that members of the RAR- receptor family modulate HSC-T6 CRBP expression. Thus, HSC-T6 cells display the same retinoid-related phenotype as primary stellate cells in culture and will be a useful tool for study of hepatic retinoid storage and metabolism.
KW - Cellular retinol-binding protein, type I (CRBP-I)
KW - Fat-storing cells
KW - Hepa-1 hepatocytes
KW - Hepatic cells
KW - Ito cells
KW - Oleic acid
KW - Retinoid nuclear receptor
KW - Retinol-binding protein (RBP)
KW - Transthyretin (TTR)
KW - Vitamin A
UR - http://www.scopus.com/inward/record.url?scp=0033921113&partnerID=8YFLogxK
U2 - 10.1016/s0022-2275(20)32030-7
DO - 10.1016/s0022-2275(20)32030-7
M3 - Article
C2 - 10828080
AN - SCOPUS:0033921113
SN - 0022-2275
VL - 41
SP - 882
EP - 893
JO - Journal of Lipid Research
JF - Journal of Lipid Research
IS - 6
ER -