Ray Denise M, Akbiyik Filiz, Bernstein Steven H, Phipps Richard P
Department of Environmental Medicine, The Lung Biology and Disease Program, University of Rochester Medical Center, School of Medicine and Dentistry, NY 14642, USA.
J Immunol. 2005 Apr 1;174(7):4060-9. doi: 10.4049/jimmunol.174.7.4060.
Peroxisome proliferator-activated receptor gamma (PPARgamma) is a transcription factor important in fat metabolism and is emerging as an important regulator of immunity and inflammation. We previously demonstrated that normal and malignant B lineage cells express PPARgamma and die by apoptosis after PPARgamma agonist exposure. In this study, we used the WEHI-231 mouse B lymphoma and normal mouse spleen B lymphocytes to elucidate the mechanism of PPARgamma agonist-induced apoptosis, and to determine whether an apoptosis rescue mechanism exists. In WEHI-231 cells, the natural PPARgamma agonist 15-deoxy-Delta(12,14)-PGJ(2) and the synthetic PPARgamma agonist ciglitazone induced activation of caspase 3 and caspase 9, a decrease in mitochondrial membrane potential, and caused cleavage of the caspase substrate poly(ADP-ribose) polymerase. We next tested whether CD40, whose engagement delivers a potent prosurvival signal for B cells, could protect B cells from PPARgamma agonist-induced apoptosis. CD40 engagement with CD40L significantly blunted the ability of PPARgamma agonists to induce apoptosis of B lymphocytes and prevented the inhibition of NF-kappaB mobilization by 15-deoxy-Delta(12,14)-PGJ(2) and ciglitazone. Interestingly, PPARgamma agonists induced an increase in IkappaBalpha and IkappaBbeta protein levels, which was prevented with CD40 engagement. The rescue mechanism induced by CD40 engagement was dependent on NF-kappaB, as an NF-kappaB inhibitor prevented rescue. Apoptosis induction by PPARgamma ligands may be important for immune regulation by killing B lymphocytes as a rapid means to dampen inflammation. Moreover, the ability of PPARgamma agonists to kill malignant B lineage cells has implications for their use as anti-B lymphoma agents.
过氧化物酶体增殖物激活受体γ(PPARγ)是脂肪代谢中一种重要的转录因子,正逐渐成为免疫和炎症的重要调节因子。我们之前证明,正常和恶性B淋巴细胞系细胞表达PPARγ,在暴露于PPARγ激动剂后会通过凋亡死亡。在本研究中,我们使用WEHI-231小鼠B淋巴瘤细胞和正常小鼠脾脏B淋巴细胞来阐明PPARγ激动剂诱导凋亡的机制,并确定是否存在凋亡挽救机制。在WEHI-231细胞中,天然PPARγ激动剂15-脱氧-Δ(12,14)-前列腺素J2(15-deoxy-Delta(12,14)-PGJ(2))和合成PPARγ激动剂吡格列酮可诱导半胱天冬酶3和半胱天冬酶9的激活,线粒体膜电位降低,并导致半胱天冬酶底物聚(ADP-核糖)聚合酶的裂解。接下来,我们测试了CD40(其结合可为B细胞传递强大的促生存信号)是否能保护B细胞免受PPARγ激动剂诱导的凋亡。CD40与CD40配体的结合显著削弱了PPARγ激动剂诱导B淋巴细胞凋亡的能力,并阻止了15-脱氧-Δ(12,14)-PGJ(2)和吡格列酮对核因子κB(NF-κB)动员的抑制作用。有趣的是,PPARγ激动剂可诱导IkappaBα和IkappaBβ蛋白水平升高,而CD40结合可阻止这种升高。CD40结合诱导的挽救机制依赖于NF-κB,因为NF-κB抑制剂可阻止挽救。PPARγ配体诱导的凋亡可能通过杀死B淋巴细胞作为减轻炎症的快速手段,对免疫调节很重要。此外,PPARγ激动剂杀死恶性B淋巴细胞系细胞的能力对其作为抗B淋巴瘤药物的应用具有重要意义。