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Cadmium (Cd2+) disrupts Ca(2+)-dependent cell-cell junctions and alters the pattern of E-cadherin immunofluorescence in LLC-PK1 cells.

作者信息

Prozialeck W C, Niewenhuis R J

机构信息

Department of Pharmacology, Chicago College of Osteopathic Medicine, Downers Grove, IL 60515.

出版信息

Biochem Biophys Res Commun. 1991 Dec 31;181(3):1118-24. doi: 10.1016/0006-291x(91)92054-n.

DOI:10.1016/0006-291x(91)92054-n
PMID:1764062
Abstract

Recent findings from our laboratories have shown that Cd2+ has relatively specific damaging effects on the adhering and occluding junctions in the established porcine renal epithelial cell line, LLC-PK1. Results of the present studies show that the junction-perturbing effects of Cd2+ in LLC-PK1 cells are more pronounced when Cd2+ is applied to the basolateral cell surface than when it is applied to the apical surface, and that the severity of the effects is inversely related to the concentration of Ca2+ in the medium. Additional results show that exposure to sublethal concentrations of Cd2+ decreases the amount of E-cadherin that is associated with cell-cell contacts. These results suggest that Cd2+ damages Ca(2+)-dependent cell-cell junctions in LLC-PK1 cells by interacting with E-cadherin or a similar Ca(2+)-sensitive site that is oriented toward the basolateral cell surface.

摘要

相似文献

1
Cadmium (Cd2+) disrupts Ca(2+)-dependent cell-cell junctions and alters the pattern of E-cadherin immunofluorescence in LLC-PK1 cells.
Biochem Biophys Res Commun. 1991 Dec 31;181(3):1118-24. doi: 10.1016/0006-291x(91)92054-n.
2
Cadmium (Cd2+) disrupts E-cadherin-dependent cell-cell junctions in MDCK cells.镉(Cd2+)会破坏MDCK细胞中依赖E-钙黏蛋白的细胞间连接。
In Vitro Cell Dev Biol Anim. 1997 Jul-Aug;33(7):516-26. doi: 10.1007/s11626-997-0094-2.
3
Ultrastructural characterization of the early changes in intercellular junctions in response to cadmium (Cd2+) exposure in LLC-PK1 cells.
Toxicol Appl Pharmacol. 1997 Jan;142(1):1-12. doi: 10.1006/taap.1996.8026.
4
Cadmium (Cd2+) disrupts intercellular junctions and actin filaments in LLC-PK1 cells.
Toxicol Appl Pharmacol. 1991 Jan;107(1):81-97. doi: 10.1016/0041-008x(91)90333-a.
5
Surface binding and uptake of cadmium (Cd2+) by LLC-PK1 cells on permeable membrane supports.LLC-PK1细胞在可渗透膜载体上对镉(Cd2+)的表面结合与摄取。
Arch Toxicol. 1993;67(2):113-9. doi: 10.1007/BF01973681.
6
The cadmium-induced disruption of tight junctions in LLC-PK1 cells does not result from apoptosis.镉诱导的LLC - PK1细胞紧密连接破坏并非由凋亡引起。
Life Sci. 1995;57(15):PL199-204. doi: 10.1016/0024-3205(95)02109-v.
7
Cadmium is more toxic to LLC-PK1 cells than to MDCK cells acting on the cadherin-catenin complex.
Am J Physiol. 1998 Jul;275(1):F143-53. doi: 10.1152/ajprenal.1998.275.1.F143.
8
Comparison of the cytotoxic effects of cadmium chloride and cadmium-metallothionein in LLC-PK1 cells.
Life Sci. 1993;53(20):PL337-42. doi: 10.1016/0024-3205(93)90567-m.
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Binding of cadmium (Cd2+) to E-CAD1, a calcium-binding polypeptide analog of E-cadherin.镉(Cd2+)与E-CAD1(一种E-钙黏蛋白的钙结合多肽类似物)的结合。
Life Sci. 1996;58(20):PL325-30. doi: 10.1016/0024-3205(96)00159-2.
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Cadmium uptake by cells of renal origin.
J Biol Chem. 1990 Dec 15;265(35):21764-70.

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