RELATIVE TOXICITIES OF PARTICULATE AND SOLUBLE FORMS OF BERYLLIUM TO A RAT-LIVER PARENCHYMAL-CELL LINE IN CULTURE AND POSSIBLE MECHANISMS OF UPTAKE

被引:25
作者
SKILLETER, DN
PAINE, AJ
机构
[1] Medical Research Council Toxicology Unit, Canhalton, Surrey SMS 4EF, Woodmansterne Road
关键词
D O I
10.1016/0009-2797(79)90100-5
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
The relative toxicities oi participate beryllium phosphate, soluble beryllium sulphate and a beryllium sulphosalicylate complex to a rat liver parenchymal derived cell line have been examined in culture. Due to the propensity of beryllium salts to form beryllium phosphate in solution the incubation medium used was free of inorganic phosphate. Cell death measured by the loss of cellular lactate dehydrogenase into the medium can be produced within 76 h from beryllium phosphate and beryllium sulphosalicylate or 48 h from beryllium sulphate provided the cells have, irrespective of the form of added beryllium, taken up a minimum of 2-5 nmol Be/106 cells. Whilst beryllium phosphate was readily taken up as a particle, beryllium complexed with excess sulphosalicylate was not so markedly accumulated by the cells except possibly by formation of small amounts of beryllium phosphate in the medium as a result of inorganic phosphate lost from the cells. The extent of beryllium uptake from beryllium sulphate quantitatively most resembled that observed for beryllium phosphate but was largely independent of beryllium phosphate formation in the medium and not accompanied by the uptake of the SO42- anion. However, the accumulation of beryllium derived from beryllium sulphate did appear to be associated with the production of a sedimentable form believed most probably to be colloidal beryllium hydroxide. The uptake of all forms of beryllium was temperature sensitive and metabolic inhibitor studies and treatment of the cells with trypsin or neuraminidase supported the view that the distinct behaviour of beryllium derived from beryllium sulphate may be related to the enhanced toxicity of this form both under the conditions used and when administered to experimental animals. © 1979.
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页码:19 / 33
页数:15
相关论文
共 19 条
[1]  
ALDRIDGE WN, 1949, BRIT J EXP PATHOL, V30, P375
[2]  
[Anonymous], CELL TISSUE CULTURE
[3]   INHIBITION OF PHAGOCYTOSIS AND PLASMA-MEMBRANE MOBILITY OF CULTIVATED MACROPHAGE BY CYTOCHALASIN-B - ROLE OF SUBPLASMALEMMAL MICROFILAMENTS [J].
AXLINE, SG ;
REAVEN, EP .
JOURNAL OF CELL BIOLOGY, 1974, 62 (03) :647-659
[4]   CRITERIA OF VIABILITY OF ISOLATED LIVER-CELLS [J].
BAUR, H ;
KASPEREK, S ;
PFAFF, E .
HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1975, 356 (06) :827-838
[5]   EXPERIMENTAL STUDIES ON THE MECHANISM OF THE ZONAL DISTRIBUTION OF BERYLLIUM LIVER NECROSIS [J].
CHENG, KK .
JOURNAL OF PATHOLOGY AND BACTERIOLOGY, 1956, 71 (02) :265-+
[6]  
Fiske CH, 1925, J BIOL CHEM, V66, P375
[7]   METABOLIC AND ENZYMATIC CHARACTERISTICS OF ADULT RAT-LIVER PARENCHYMAL-CELLS IN NON-PROLIFERATING PRIMARY MONOLAYER-CULTURES [J].
GEBHARDT, R ;
BELLEMANN, P ;
MECKE, D .
EXPERIMENTAL CELL RESEARCH, 1978, 112 (02) :431-441
[8]  
HARD G C, 1977, Experimental and Molecular Pathology, V27, P197, DOI 10.1016/0014-4800(77)90030-2
[9]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[10]   MALIGNANT TRANSFORMATION IN-VITRO OF RAT-LIVER CELLS BY DIMETHYLNITROSAMINE AND N-METHYL-N'-NITRO-N-NITROSOGUANIDINE [J].
MONTESANO, R ;
SAINTVIN.L ;
TOMATIS, L .
BRITISH JOURNAL OF CANCER, 1973, 28 (03) :215-220