Metabolic enzyme diversity in different human thyroid cell lines and their sensitivity to gravitational forces

被引:30
作者
Pietsch, Jessica [2 ]
Sickmann, Albert [3 ]
Weber, Gerhard [4 ]
Bauer, Johann [1 ]
Egli, Marcel [5 ]
Wildgruber, Robert [4 ]
Infanger, Manfred [2 ]
Grimm, Daniela [6 ]
机构
[1] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[2] Otte von Guericke Univ, Magdeburg, Germany
[3] Inst Analyt Sci, ISAS, Dortmund, Germany
[4] FFE Serv GmbH, Munich, Germany
[5] Swiss Fed Inst Technol, Space Biol Grp, Zurich, Switzerland
[6] Aarhus Univ, Inst Biomed, Aarhus, Denmark
关键词
Cell biology; Free-flow electrophoresis; Simulated microgravity; Thyroid cancer; RANDOM POSITIONING MACHINE; ENDOTHELIAL GROWTH-FACTOR; SIMULATED MICROGRAVITY; CARCINOMA CELLS; ALPHA-ENOLASE; CANCER-CELLS; EXTRACELLULAR-MATRIX; PROTEOMIC APPROACH; CYCLE ENZYMES; C-MYC;
D O I
10.1002/pmic.201200070
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Many cancer cells show unique protein expression patterns. We used proteome technology including MS, free flow isoelectric focusing and Western blotting to determine current concentrations of metabolic enzymes in healthy and malignant human thyroid cells. Three different types of human thyroid cells were investigated after they had been cultured under equal conditions. MS revealed high quantities of glycolytic enzymes and moderate quantities of citric acid cycle enzymes in malignant FTC-133 cells with abnormal LDH B-chains, high quantities of glycolytic enzymes and marginal quantities of citric acid cycle enzymes in normal HTU-5 cells, and low quantities of glycolytic enzymes and marginal quantities of citrate cycle enzymes in malignant CGTH-W1 cells with abnormal LDH A-chains. When an alteration of gene expression activity was challenged physically by removing gravity forces, the concentrations of various glycolytic enzymes were changed in normal and malignant thyroid cells. However, the changes varied among the different cell types. Different cellular alignment of the enzymes could be one reason for the cell type-specific behavior as demonstrated by histological analysis of alpha-enolase.
引用
收藏
页码:2539 / 2546
页数:8
相关论文
共 45 条
[1]  
Boyer H. S., 1963, AIDS RES HUM RETRO S, V141, P642
[2]   α-enolase: a promising therapeutic and diagnostic tumor target [J].
Capello, Michela ;
Ferri-Borgogno, Sammy ;
Cappello, Paola ;
Novelli, Francesco .
FEBS JOURNAL, 2011, 278 (07) :1064-1074
[3]   Function and structure of complex II of the respiratory chain [J].
Cecchini, G .
ANNUAL REVIEW OF BIOCHEMISTRY, 2003, 72 :77-109
[4]   c-Myc is required for the glucose-mediated induction of metabolic enzyme genes [J].
Collier, JJ ;
Doan, TTT ;
Daniels, MC ;
Schurr, JR ;
Kolls, JK ;
Scott, DK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) :6588-6595
[5]   LONG-TERM CULTURE AND FUNCTIONAL-CHARACTERIZATION OF FOLLICULAR CELLS FROM ADULT NORMAL HUMAN THYROIDS [J].
CURCIO, F ;
AMBESIIMPIOMBATO, FS ;
PERRELLA, G ;
COON, HG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (19) :9004-9008
[6]   MCT1 and its accessory protein CD147 are differentially regulated by TSH in rat thyroid cells [J].
Fanelli, A ;
Grollman, EF ;
Wang, D ;
Philp, NJ .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2003, 285 (06) :E1223-E1229
[7]   Fine-needle aspiration of thyroid nodules: Proteomic analysis to identify cancer biomarkers [J].
Giusti, Laura ;
Iacconi, Pietro ;
Ciregia, Federica ;
Giannaccini, Gino ;
Donatini, Gian Luca ;
Basolo, Fulvio ;
Miccoli, Paolo ;
Pinchera, Aldo ;
Lucacchini, Antonio .
JOURNAL OF PROTEOME RESEARCH, 2008, 7 (09) :4079-4088
[8]  
Goretzki P E, 1990, Recent Results Cancer Res, V118, P48
[9]   Diagnostic and Therapeutic Use of Membrane Proteins in Cancer Cells [J].
Grimm, D. ;
Bauer, J. ;
Pietsch, J. ;
Infanger, M. ;
Eucker, J. ;
Eilles, C. ;
Schoenberger, J. .
CURRENT MEDICINAL CHEMISTRY, 2011, 18 (02) :176-190
[10]   Characteristics of multicellular spheroids formed by primary cultures of human thyroid tumor cells [J].
Grimm, D ;
Bauer, J ;
Hofstadter, F ;
Riegger, GAJ ;
Kromer, EP .
THYROID, 1997, 7 (06) :859-865