CLC number: R995
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
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ZHANG Ying, YE Li-ping, WANG Biao, CAO Shi-cheng, SUN Li-guang. Effect of lead on ERK activity and the protective function of bFGF in rat primary culture astroglia[J]. Journal of Zhejiang University Science B, 2007, 8(6): 422-427.
@article{title="Effect of lead on ERK activity and the protective function of bFGF in rat primary culture astroglia",
author="ZHANG Ying, YE Li-ping, WANG Biao, CAO Shi-cheng, SUN Li-guang",
journal="Journal of Zhejiang University Science B",
volume="8",
number="6",
pages="422-427",
year="2007",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.2007.B0422"
}
%0 Journal Article
%T Effect of lead on ERK activity and the protective function of bFGF in rat primary culture astroglia
%A ZHANG Ying
%A YE Li-ping
%A WANG Biao
%A CAO Shi-cheng
%A SUN Li-guang
%J Journal of Zhejiang University SCIENCE B
%V 8
%N 6
%P 422-427
%@ 1673-1581
%D 2007
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.2007.B0422
TY - JOUR
T1 - Effect of lead on ERK activity and the protective function of bFGF in rat primary culture astroglia
A1 - ZHANG Ying
A1 - YE Li-ping
A1 - WANG Biao
A1 - CAO Shi-cheng
A1 - SUN Li-guang
J0 - Journal of Zhejiang University Science B
VL - 8
IS - 6
SP - 422
EP - 427
%@ 1673-1581
Y1 - 2007
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.2007.B0422
Abstract: Objective: To observe the effects of lead on levels of phosphorylated extracellular signal regulated kinase (p-ERK) in the cytoplasm of primary cultures of rat astroglial cells and the possible protective effect of basic fibroblast growth factor (bFGF) on lead-induced effects. Methods: The primary astroglia cells from 1~6 d old Wistar rats were cultured. The cells pretreated with the MEK1 (mitogen-activated protein kinase kinase 1) inhibitor PD98059 and bFGF, respectively, were exposed to Pb acetate of different concentrations for different times. Western blotting and reverse transcription polymerase chain reaction (RT-PCR) methods were used to detect the protein and mRNA expressions of ERK. Results: mRNA expression for ERK peaked 15 min after initiation of lead exposure (P<0.05) and protein expression of p-ERK peaked at 30 min (P<0.05). ERK mRNA levels and p-ERK protein levels returned to baseline after 60 and 120 min of lead exposure, respectively (P>0.05). The increase in p-ERK levels in lead-treated cells could be inhibited by PD098059. Activation of ERK in the cells by lead was prevented by pretreatment with bFGF. Total ERK protein levels did not change under the same experimental conditions (P>0.05). Conclusion: Low-level lead exposure resulted in transient activation of ERK through the MEK pathway, which then returned to basal levels in the continued presence of lead. Exogenous bFGF protected ERK signaling components in astroglia from lead poisoning.
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