TY - JOUR
T1 - Expression of cystatin C prevents oxidative stress-induced death in PC12 cells
AU - Nishiyama, Keiji
AU - Konishi, Akio
AU - Nishio, Chika
AU - Araki-Yoshida, Kiyomi
AU - Hatanaka, Hiroshi
AU - Kojima, Masami
AU - Ohmiya, Yoshihiro
AU - Yamada, Masashi
AU - Koshimizu, Hisatsugu
N1 - Funding Information:
The authors thank Hitoshi Aoshima for providing LOOH. This work was supported by grants-in-aid for scientific research from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
PY - 2005/9/30
Y1 - 2005/9/30
N2 - Cystatin C, an inhibitor of cysteine proteinases, is suggested to be involved in oxidative stress-induced apoptosis of cultured CNS neurons and various neuronal diseases in vivo; however, little is known about its mechanism of action. To address the role cystatin C plays in oxidative stress-induced neuronal cell death, we established PC12 cell lines that stably expressed rat cystatin C. These cystatin C-expressing PC12 cells showed remarkable resistance to high (50%) oxygen atmosphere. This resistance correlate with expression levels of cystatin C, demonstrating that cystatin C has a protective effect on high oxygen-induced cell death. In contrast, in a normal (20%) oxygen atmosphere neither control nor cystatin C-expressing PC12 cells showed a significant change in the number of living cells, indicating that cystatin C does not play an important role in the regulation of cellular proliferation. Furthermore, the cystatin C-expressing cell line also resisted other oxidative stresses, including glutamate- and 13-l-hydroperoxylinoleic acid (LOOH)-induced cell death. These results demonstrate that cystatin C has protective effects against various oxidative stresses that induce cell death.
AB - Cystatin C, an inhibitor of cysteine proteinases, is suggested to be involved in oxidative stress-induced apoptosis of cultured CNS neurons and various neuronal diseases in vivo; however, little is known about its mechanism of action. To address the role cystatin C plays in oxidative stress-induced neuronal cell death, we established PC12 cell lines that stably expressed rat cystatin C. These cystatin C-expressing PC12 cells showed remarkable resistance to high (50%) oxygen atmosphere. This resistance correlate with expression levels of cystatin C, demonstrating that cystatin C has a protective effect on high oxygen-induced cell death. In contrast, in a normal (20%) oxygen atmosphere neither control nor cystatin C-expressing PC12 cells showed a significant change in the number of living cells, indicating that cystatin C does not play an important role in the regulation of cellular proliferation. Furthermore, the cystatin C-expressing cell line also resisted other oxidative stresses, including glutamate- and 13-l-hydroperoxylinoleic acid (LOOH)-induced cell death. These results demonstrate that cystatin C has protective effects against various oxidative stresses that induce cell death.
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U2 - 10.1016/j.brainresbull.2005.05.020
DO - 10.1016/j.brainresbull.2005.05.020
M3 - Article
C2 - 16140167
AN - SCOPUS:24044535122
SN - 0361-9230
VL - 67
SP - 94
EP - 99
JO - Brain Research Bulletin
JF - Brain Research Bulletin
IS - 1-2
ER -