Lead exposure in pheochromocytoma (PC12) cells alters neural differentiation and Sp1 DNA-binding

被引:48
作者
Crumpton, T
Atkins, DS
Zawia, NH [1 ]
Barone, S
机构
[1] Univ Rhode Isl, Dept Biomed Sci, Kingston, RI 02881 USA
[2] Meharry Med Coll, Dept Pharmacol, Nashville, TN 37208 USA
[3] US EPA, Cellular & Mol Toxicol Branch, Div Neurotoxicol, Res Triangle Pk, NC 27711 USA
关键词
neurite outgrowth; lead neurotoxicity; Sp1; NGF; nerve growth factor;
D O I
10.1016/S0161-813X(00)00008-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previous studies have revealed that lead modulates the DNA-binding profile of the transcription factor Sp1 both in vivo and in vitro (Dev Brain Res 1998;107:291). Sp1 is a zinc finger protein, that is selectively up-regulated in certain developing cell types and plays a regulatory role during development and differentiation (Mol Cell Biol 1992;11:2189). In NGF-stimulated PC12 cells, Sp1 DNA-binning activity was induced within 48 h of exposure of NGF naive cells. Exposure of undifferentiated PC12 cells to lend alone (0.1 muM) also produced a similar increase in Sp1 DNA-binding. Since lend altered the DNA-binding profile of Sp1 bl newly differentiating cells, neurite outgrowth,vas assessed as a morphological marker of differentiation to determine whether or not the effects of lead on differentiation were restricted to the initiation phase (unprimed) or the elaboration phase of this process (NGF-primed). NGF-primed and unprimed PC12 cells were prepared for bioassay following exposure to various concentrations of NGF and/or lead. Neurite outgrowth was measured at 48 and 72 h during early stages of NGF-induced differentiation and at 14 h in NGF primed/replated cells. In the absence of NGF: exposure to lead alone (0.025, 0.05, 0.1 muM) promoted measurable neurite outgrowth in unprimed PC12 cells at 48 and 72 h. A similar-phenomenon was also observed in primed/replated PC12 cells at 14 h. However; this effect was two to Jive times greater than unprimed control cells. In the presence of NGF; a similar trend was apparent at lower concentrations, although the magnitude and temporal nature was different from? lead alone. In most cases, the administration of higher lead concentrations (1 and 20 muM), in both the absence or presence of NGF: was less effective than the lower concentrations in potentiating neurite outgrowth. These results suggest that lead alone at low doses may initiate premature stimulation of morphological differentiation that may be related to lead-induced alterations in Spl binding to DNA. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
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页码:49 / 62
页数:14
相关论文
共 71 条
[1]   NEONATAL LEAD-EXPOSURE ALTERS THE DENDRITIC DEVELOPMENT OF HIPPOCAMPAL DENTATE GRANULE CELLS [J].
ALFANO, DP ;
PETIT, TL .
EXPERIMENTAL NEUROLOGY, 1982, 75 (02) :275-288
[2]  
AVERILL D, 1980, LOW LEVEL LEAD EXPOS, P210
[3]   FUNCTIONAL-ANALYSIS OF THE PROXIMAL 5'-FLANKING REGION OF THE N-METHYL-D-ASPARTATE RECEPTOR SUBUNIT GENE, NMDAR1 [J].
BAI, G ;
KUSIAK, JW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (13) :7737-7744
[4]  
Barone S, 2000, NEUROTOXICOLOGY, V21, P15
[5]   GROWTH-FACTORS AND MEMBRANE DEPOLARIZATION ACTIVATE DISTINCT PROGRAMS OF EARLY RESPONSE GENE-EXPRESSION - DISSOCIATION OF FOS AND JUN INDUCTION [J].
BARTEL, DP ;
SHENG, M ;
LAU, LF ;
GREENBERG, ME .
GENES & DEVELOPMENT, 1989, 3 (03) :304-313
[6]  
BORELLINI F, 1993, J BIOL CHEM, V268, P7923
[7]   DIFFERENTIAL VULNERABILITY OF MIXED AND CUTANEOUS NERVES IN LEAD NEUROPATHY [J].
BOULDIN, TW ;
MEIGHAN, ME ;
GAYNOR, JJ ;
GOINES, ND ;
MUSHAK, P ;
KRIGMAN, MR .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1985, 44 (04) :384-396
[8]   PURIFICATION AND BIOCHEMICAL-CHARACTERIZATION OF THE PROMOTER-SPECIFIC TRANSCRIPTION FACTOR, SPL [J].
BRIGGS, MR ;
KADONAGA, JT ;
BELL, SP ;
TJIAN, R .
SCIENCE, 1986, 234 (4772) :47-52
[9]   NEONATAL LEAD-EXPOSURE IN RAT - DECREASED LEARNING AS A FUNCTION OF AGE AND BLOOD LEAD CONCENTRATIONS [J].
BROWN, DR .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1975, 32 (03) :628-637
[10]  
BULL RJ, 1983, NEUROTOXICOLOGY, V4, P1