Abstract |
Intraperitoneal injection of the hydrocarbon oil pristane into normal mice leads to a lupus-like autoimmune syndrome. Although advances in defining the roles of cellular and humoral mediators involved in this syndrome have been made, the mechanisms that initiate a break in tolerance leading to autoimmunity remain unknown. We describe in this study that pristane induces apoptosis both in vivo and in vitro. Pristane arrests cell growth and induces cell death by apoptosis via the mitochondrial pathway of caspase activation in a dose-dependent manner. Nuclear autoantigens created by pristane-induced apoptosis of lymphoid cells within the peritoneal cavity in the setting of a profoundly altered cytokine milieu may be the initiating event in the development of autoimmunity in this syndrome. These findings suggest that apoptosis may be a critical initial event in the pathogenesis of pristane-induced lupus and are of potential relevance for human systemic lupus erythematosus.
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Authors | Nicola Calvani, Roberto Caricchio, Marco Tucci, Eric S Sobel, Franco Silvestris, Paola Tartaglia, Hanno B Richards |
Journal | Journal of immunology (Baltimore, Md. : 1950)
(J Immunol)
Vol. 175
Issue 7
Pg. 4777-82
(Oct 01 2005)
ISSN: 0022-1767 [Print] United States |
PMID | 16177126
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
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Topics |
- Animals
- Apoptosis
(drug effects)
- Ascitic Fluid
(metabolism)
- Cell Line, Tumor
- Dose-Response Relationship, Drug
- Female
- Humans
- Injections, Intraperitoneal
- Jurkat Cells
- Lupus Erythematosus, Systemic
(chemically induced, pathology)
- Lymphocytes
(drug effects)
- Mice
- Mice, Inbred BALB C
- Mice, Inbred C57BL
- Mitochondria
(drug effects)
- Terpenes
(administration & dosage, pharmacology)
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