Associations between Lead Exposure and Dose and Protein Kinase C Activation in Erythrocytes Among Lead Workers.
- Author:
Kyu Yoon HWANG
1
;
Young HWANGBO
;
Hyun Cheol AHN
;
Yong Bae KIM
;
Gap Soo LEE
;
Sung Soo LEE
;
Kyu Dong AHN
;
Byung Kook LEE
Author Information
1. Department of Preventive Medicine, School of Medicine, Soonchunhyang University, Korea. drhwang@sch.ac.kr
- Publication Type:In Vitro ; Original Article
- Keywords:
Lead;
Tibial lead;
Protein kinase C;
Biomarker;
Back phosphorylation
- MeSH:
Calcium;
Erythrocyte Membrane;
Erythrocytes*;
Humans;
Luminescence;
Phosphorylation;
Protein Kinase C*;
Protein Kinases*;
Spectrin
- From:Korean Journal of Occupational and Environmental Medicine
2001;13(4):369-375
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVES: Protein kinase C(PKC), a calcium and phospholipid dependent enzyme, is activated by lead in vitro at picomolar concentrations. However, the effect of lead on PKC has never been studied in a human population. The purpose of the study was to evaluate whether lead exposure was associated with PKC mediated-phosphorylation in erythrocytes among lead workers. METHODS: Two hundred and twelve lead workers were studied. To determine the levels of phosphorylation in vivo, an in vitro back phosphorylation technique was used by adding PKC and gamma-32P to preparations of erythrocyte membranes. We measured back phosphorylations of erythrocyte membrane proteins, spectrin, and 52 kDa and 48 kDa, as an indirect measure of PKC activation in vivo. RESULTS: The mean(SD) age and exposure duration was 39.1(10.0) years and 8.1(6.5) years, respectively. Tibial lead ranged from 0.8 to 290.8 microgram Pb/g bone mineral with a mean(SD) of 34.4(35.2) microgram Pb/g bone mineral. The means(SD) of back phosphorylation levels of the three proteins were 540.7(304.1), 198.6(78.2), and 247.7(83.3) photostimulated luminescence units(PSL), respectively, by phosphoimager. After adjustment for potential confounding factors, tibial lead and exposure duration were significantly and inversely associated with back phosphorylation levels. One unit of increase in tibial lead(1 microgram Pb/g bone mineral) is associated with a decline in spectrin, band 4.9 52 kDa, and band 4.9 48 kDa back phosphorylation levels by 1.4(P<0.05), 0.34(P<0.05), and 0.47(P<0.01), respectively. However, there were no associations between the back phosphorylation levels and either blood lead or ZPP levels. CONCLUSIONS: These findings suggest that the PKC activity in erythrocytes is increased by chronic lead exposure and that erythrocyte membrane protein phosphorylation may be a biomarker of lead exposure.
