PDTC Inhibits TNF-alpha-Induced Apoptosis in MC3T3E1 Cells
The Korean Journal of Physiology and Pharmacology
; : 199-206, 2003.
Artículo
en Inglés
| WPRIM (Pacífico Occidental)
| ID: wpr-727902
Biblioteca responsable:
WPRO
ABSTRACT
Osteoblasts are affected by TNF-alpha overproduction by immune cells during inflammation. It has been suggested that functional NF-kappaB sites are involved in TNF-alpha-induced bone resorption. Thus, we explored the effect of pyrrolidine dithiocarbamate (PDTC), which potently blocks the activation of nuclear factor (NF-kappaB), on the induction of TNF-alpha-induced activation of JNK/SAPK, AP-1, cytochrome c, caspase and apoptosis in MC3T3E1 osteoblasts. Pretreatment of the cells with PDTC blocked TNF-alpha-induced NF-kappaB activation. TNF-alpha-induced activation of AP-1, another nuclear transcription factor, was suppressed by PDTC. The activation of c-Jun N-terminal kinase, implicated in the regulation of AP-1, was also down regulated by PDTC. TNF-alpha-induced apoptosis, release of cytochrome c and subsequent activation of caspase-3 were abolished by PDTC. TNF-alpha-induced apoptosis was partially blocked by Ac-DEVD-CHO, a caspase-3 inhibitor, suggesting that caspase-3 is involved in TNF-alpha- mediated signaling through NF-kappaB in MC3T3E1 osteoblasts. Thus, these results demonstrate that PDTC, has an inhibitory effect on TNF-alpha-mediated activation of JNK/SAPK, AP-1, cytochrome c release and subsequent caspase-3, leading to the inhibition of apoptosis. Our study may contribute to the treatment of TNF-alpha-associated immune and inflammatory diseases such as rheumatoid arthritis and periodontal diseases.
Texto completo:
Disponible
Base de datos:
WPRIM (Pacífico Occidental)
Asunto principal:
Osteoblastos
/
Enfermedades Periodontales
/
Artritis Reumatoide
/
Factores de Transcripción
/
Resorción Ósea
/
FN-kappa B
/
Factor de Necrosis Tumoral alfa
/
Apoptosis
/
Factor de Transcripción AP-1
/
Citocromos c
Idioma:
Inglés
Revista:
The Korean Journal of Physiology and Pharmacology
Año:
2003
Tipo del documento:
Artículo