Induction of ferritin synthesis in human lung epithelial cells treated with crocidolite asbestos

被引:52
作者
Fang, RH [1 ]
Aust, AE [1 ]
机构
[1] UTAH STATE UNIV, DEPT CHEM & BIOCHEM, LOGAN, UT 84322 USA
关键词
asbestos; crocidolite; ferritin induction; iron incorporation into ferritin; A549; cells; human lung epithelial cells; low-molecular-weight iron;
D O I
10.1006/abbi.1997.9892
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Crocidolite asbestos is a known human carcinogen containing 27% iron by weight. It has previously been shown that iron was mobilized intracellularly from crocidolite after treatment of human lung epithelial cells (A549) and that the toxicity of the fibers was directly related to how much mobilized iron was in the <10,000 MW (low-molecular-weight, LMW) fraction [C. C. Chao, L. G. Lund, K. Il. Zinn, and A. E. Aust (1994) Arch. Biochem. Biophys. 314, 384-391]. The data here show that iron mobilization from crocidolite began immediately after treatment of the A549 cells and increased linearly with time. However, the synthesis of ferritin, an iron storage protein, did not begin until after 4 h of treatment, reaching a sustained maximum after 12 h. Mobilized iron was preferentially incorporated into the non-ferritin-protein fraction up to 7 h after treatment, when the amount of iron mobilized was low and before significant accumulation of newly synthesized ferritin had occurred,This suggested that these cultured cells needed additional iron for synthesis of iron-requiring proteins and that iron mobilized from crocidolite could be utilized directly for this purpose. Subsequent to this, additional mobilized iron was incorporated into newly synthesized ferritin. Even though iron from crocidolite was incorporated into newly synthesized ferritin or into other proteins, the amount of iron from crocidolite in the LMW fraction remained constant during the 24 h. Thus, it appeared that synthesis of ferritin may not have fully protected the cells from the toxic effects of iron mobilized from crocidolite. (C) 1997 Academic Press.
引用
收藏
页码:369 / 375
页数:7
相关论文
共 33 条
[1]  
AUST AE, 1991, NATO ADV SCI I A-LIF, V223, P397
[2]   ENDOTHELIAL-CELL HEME OXYGENASE AND FERRITIN INDUCTION IN RAT LUNG BY HEMOGLOBIN IN-VIVO [J].
BALLA, J ;
NATH, KA ;
BALLA, G ;
JUCKETT, MB ;
JACOB, HS ;
VERCELLOTTI, GM .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1995, 268 (02) :L321-L327
[3]   Participation of nitric oxide and iron in the oxidation of DNA in asbestos-treated human lung epithelial cells [J].
Chao, CC ;
Park, SH ;
Aust, AE .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1996, 326 (01) :152-157
[4]   IRON MOBILIZATION FROM CROCIDOLITE ASBESTOS BY HUMAN LUNG-CARCINOMA CELLS [J].
CHAO, CC ;
LUND, LG ;
ZINN, KR ;
AUST, AE .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1994, 314 (02) :384-391
[5]  
CRICHTON RR, 1991, INORGANIC BIOCH IRON, P154
[6]   UPTAKE AND INTRACELLULAR HANDLING OF IRON FROM TRANSFERRIN AND IRON CHELATES BY MITOGEN STIMULATED MOUSE LYMPHOCYTES [J].
DJEHA, A ;
BROCK, JH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1133 (02) :147-152
[7]  
DRYSDALE JW, 1966, J BIOL CHEM, V241, P3630
[8]   REGULATION OF FERRITIN AND HEME OXYGENASE SYNTHESIS IN RAT FIBROBLASTS BY DIFFERENT FORMS OF IRON [J].
EISENSTEIN, RS ;
GARCIAMAYOL, D ;
PETTINGELL, W ;
MUNRO, HN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (03) :688-692
[9]  
GOTO Y, 1983, J BIOL CHEM, V258, P5248
[10]  
HABERLAND ME, 1992, FREE RADICAL MECH TI, P45