A Study of the Regulation of the Glucose Transporter in the Plasma Membranes of Hepatoma Cells Induced by 3'-Me DAB.
10.3349/ymj.1987.28.3.192
- Author:
Yong Ho AHN
1
;
Kyung Ja CHAI
;
Soo Nyung KIM
;
Yoon Soo KIM
Author Information
1. Department of Biochemistry, Yonsei University College of Medicine, Seoul, Korea.
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Glucose transport;
5'-nucleotidase;
glucose-6-phosphatase;
cytochalasin 8
- MeSH:
Animal;
Cell Membrane/enzymology;
Cell Membrane/metabolism;
Liver Neoplasms, Experimental/metabolism*;
Male;
Methyldimethylaminoazobenzene*;
Microsomes, Liver/enzymology;
Microsomes, Liver/metabolism;
Monosaccharide Transport Proteins/isolation & purification;
Monosaccharide Transport Proteins/metabolism*;
Rats;
Rats, Inbred Strains;
p-Dimethylaminoazobenzene*/analogs & derivatives
- From:Yonsei Medical Journal
1987;28(3):192-198
- CountryRepublic of Korea
- Language:English
-
Abstract:
5'-nucelotidase and glucose-6-phosphatase are liver plasma and microsomal membranes markers and their respective activities were determined. In the liver homogenate, the activities of 5'-nucleotidase were 0.58 +/- 0.08 and 0.29 +/- 0.07 micromols/mg protein/10min in the control and 3'-methyl-4-dimethyl aminoazobenzene (3'-Me DAB) groups respectively. The enzyme activities m the partially purified plasma membranes were 2.15 +/- 0.25 and 1.31 +/- 0.23 micromols/mg protein/10min in the control and 3'-Me DAB groups respectively. The glucose-6-phosphatase activities in the homogenates of the control and 3'-Me DAB groups were 0.23 +/- 0.10, and 0.45 +/- 0.25 micromols/mg protein/10min, and in the microsomal fraction, 1.14 +/- 0.32, and 0.63 +/- 0.11 micromols/mg protein/10min, respectively, The concentrations of glucose carrier in the plasma membranes from the control and 3'-Me DAB group were 25, and 35 pmols/mg membrane protein, respectively, and the Ka values for cytochalsin B in each group were 5.20 X 109. and 5.14 X 109ml/mol, respectively. However in the microsomal fraction, no significant differences of glucose carrier were found between the control and 3'-Me DAB groups from the DEAE Sephadex A-50 ion exchange chromatography, fractions I and ll were obtained. Electrophoretic analysis of fraction I revealed a major protein band with a molecular weight of 45,000 and minor bands with MWs of 50,000, 55,000 and 15,000. Following AcA 34 gel filtration, a major protein band with a MW of 45,000 was obtained. From these results, it can be concluded that the glucose carrier protein was increased on plasma membrane of hepatoma induced by 3'-Me DAB, and the carrier protein showed similar molecular weight to other glucose carrier found in the RBC, muscle cells and adipocyte.
