The role of endoplasmic reticulum in cadmium-induced mesangial cell apoptosis

Sheng Hao Wang, Yung Luen Shih, Chin Cheng Lee, Wei Li Chen, Chein Ju Lin, Yung Sheng Lin, Kuan Hsun Wu, Chwen Ming Shih

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Abstract

Cd is an industrial and environmental pollutant that affects many organs in humans and other mammals. However, the molecular mechanisms of Cd-induced nephrotoxicity are unclear. In this study, we show that endoplasmic reticula (ER) played a pivotal role in Cd-induced apoptosis in mesangial cells. Using Fluo-3 AM, the intracellular concentration of calcium ([Ca2+]i) was detected as being elevated as time elapsed after Cd treatment. Co-treatment with BAPTA-AM, a calcium chelator, was able to significantly suppress Cd-induced apoptosis. Calcineurin is a cytosolic phosphatase, which was able to dephosphorylate the inositol-1,4,5-triphosphate receptor (IP3R) calcium channel to prevent the release of calcium from ER. Cyclosporine A, a calcineurin inhibitor, increased both [Ca2+]i and the percentage of Cd-induced apoptosis. However, EGTA and the IP3R inhibitor, 2-APB, were able to partially modulate Cd cytotoxicity. These results led us to suggest that the extracellular and ER-released calcium plays a crucial role in Cd-induced apoptosis in mesangial cells. Following this line, we further detected the ER stress after Cd treatment since ER is one of the major calcium storage organelles. After Cd exposure, GADD153, a hallmark of ER stress, was upregulated (at 4 h of exposure), followed by activation of ER-specific caspase-12 and its downstream molecule caspase-3 (at 16 h of exposure). The pan caspase inhibitor, Z-VAD, and BAPTA-AM were able to reverse the Cd-induced cell death and ER stress, respectively. Furthermore, the mitochondrial membrane potential (ΔΨm) was depolarized significantly and cytochrome c was released after 24 h of exposure to Cd and followed by mild activation of caspase-9 at the 36-h time point, indicating that mitochondria stress is a late event. Therefore, we concluded that ER is the major killer organelle in Cd-induced mesangial cell apoptosis and that calcium oscillation plays a pivotal role.

Original languageEnglish
Pages (from-to)45-51
Number of pages7
JournalChemico-Biological Interactions
Volume181
Issue number1
DOIs
Publication statusPublished - Sep 14 2009

Fingerprint

Mesangial Cells
Cadmium
Endoplasmic Reticulum
Apoptosis
Calcium
Endoplasmic Reticulum Stress
Organelles
Caspase 12
Chemical activation
Inositol 1,4,5-Trisphosphate Receptors
Environmental Pollutants
Mitochondria
Mammals
Caspase Inhibitors
Caspase 9
Calcineurin
Egtazic Acid
Cell death
Calcium Channels
Cytotoxicity

Keywords

  • Apoptosis
  • Cadmium
  • Calcium
  • Endoplasmic reticula
  • Mitochondria

ASJC Scopus subject areas

  • Toxicology

Cite this

The role of endoplasmic reticulum in cadmium-induced mesangial cell apoptosis. / Wang, Sheng Hao; Shih, Yung Luen; Lee, Chin Cheng; Chen, Wei Li; Lin, Chein Ju; Lin, Yung Sheng; Wu, Kuan Hsun; Shih, Chwen Ming.

In: Chemico-Biological Interactions, Vol. 181, No. 1, 14.09.2009, p. 45-51.

Research output: Contribution to journalArticle

Wang, Sheng Hao ; Shih, Yung Luen ; Lee, Chin Cheng ; Chen, Wei Li ; Lin, Chein Ju ; Lin, Yung Sheng ; Wu, Kuan Hsun ; Shih, Chwen Ming. / The role of endoplasmic reticulum in cadmium-induced mesangial cell apoptosis. In: Chemico-Biological Interactions. 2009 ; Vol. 181, No. 1. pp. 45-51.
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