Multiple ways to die: Delineation of the unfolded protein response and apoptosis induced by Surfactant Protein C BRICHOS mutants

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• 作者：Jean Ann Maguire ; Surafel Mulugeta ; Michael F. Beers  ; ;   ; ^{mfbeers@mail.med.upenn.edu}
• 关键词：BRICHOS family ; Unfolded protein response ; ER stress ; Apoptosis ; Interstitial lung disease
• 刊名：The International Journal of Biochemistry and Cell Biology
• 出版年：2012
• 出版时间：January 2012
• 年：2012
• 卷：44
• 期：1
• 页码：101-112
• 全文大小：1376 K

文摘

Epithelial cell dysfunction is now recognized as an important mechanism in the pathogenesis of interstitial lung diseases. Surfactant Protein C (SP-C), an alveolar type II cell specific protein, has contributed to this concept with the observation that heterozygous expression of lns="""">SFTPC gene mutations are associated with chronic interstitial lung disease. We have shown that transient expression of aggregation prone mutant SP-C isoforms (SP-C BRICHOS) destabilize ER quality control mechanisms resulting in the intracellular accumulation of aggregating propeptide, inhibition of the ubiquitin/proteasome system, and activation of apoptosis. The goal of the present study was to define signaling pathways linking the unfolded protein response (UPR) and subsequent ER stress with intrinsic apoptosis events observed following mutant SP-C expression. lns="""">In vitro expression of the SP-C BRICHOS mutant, SP-C^{lns="""">¦¤exon4}, was used as a model system. Here we show stimulation of a broad ER stress response in both transfected A549 and HEK293 cells with activation of all 3 canonical sensing pathways, IRE1/XBP-1, ATF6, and PERK/eIF2¦Á. SP-C^{lns="""">¦¤exon4} expression also resulted in activation of caspase 3, but failed to stimulate expression of the apoptosis mediating transcription factors ATF4/CHOP. However, inhibition of either caspase 4 or c-jun kinase (JNK) each blocked caspase 3 mediated cell death. Taken together, these results suggest that expression of SP-C BRICHOS mutants induce apoptosis through multiple UPR signaling pathways, and provide new therapeutic targets for the amelioration of ER stress induced cytotoxicity observed in fibrotic lung remodeling.