Pharmaceutical Sciences Faculty Publications
Functional Role of Interleukin 1ß (IL-1ß) in IL-1ß-converting Enzyme-mediated Apoptosis
Document Type
Article
Publication Date
8-1996
Journal Title
Journal of Experimental Medicine
Volume
184
Issue
2
First Page
717
Last Page
724
DOI
http://dx.doi.org/10.1084/jem.184.2.717
Abstract
Prointerleukin-1 beta (pro-IL-1 beta) is the only known physiologic substrate of the interleukin-1 beta (IL-1 beta)-converting enzyme (ICE), the founding member of the ICE/ced-3 cell death gene family. Since secreted mature IL-1 beta has been detected after apoptosis, we investigated whether this cytokine, when produced endogenously, plays a role in cell death. We found that hypoxia-induced apoptosis can be inhibited by either the IL-1 receptor antagonist (IL-1Ra) or by neutralizing antibodies to IL-1 or to its type 1 receptor. IL-1Ra also inhibits apoptosis induced by trophic factor deprivation in primary neurons, as well as by tumor necrosis factor alpha in fibroblasts. In addition, during the G1/S phase arrest, mature IL-1 beta induces apoptosis through a pathway independent of CrmA-sensitive gene activity. We also demonstrate that Ice, when expressed in COS cells, requires the coexpression of pro-IL-1 beta for the induction of apoptosis, which is inhibited by IL-1Ra. Interestingly, we found that mature IL-1 beta has antiapoptotic activity when added exogenously before the onset of hypoxia, which we found is caused in part by its ability to downregulate the IL-1 receptor. Our findings demonstrate that pro-IL-1 beta is a substrate of ICE relevant to cell death, and depending on the temporal cellular commitment to apoptosis, mature IL-1 beta may function as a positive or negative mediator of cell death.
Keywords
Apoptosis, enzymes, interleukin, 1 beta
Recommended Citation
Friedlander, Robert M.; Gagliardini, Valeria; Rotello, Rocco J.; and Yuan, Junying, "Functional Role of Interleukin 1ß (IL-1ß) in IL-1ß-converting Enzyme-mediated Apoptosis" (1996). Pharmaceutical Sciences Faculty Publications. 62.
https://digitalcommons.cedarville.edu/pharmaceutical_sciences_publications/62