| pubmed-article:16449190 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16449190 | lifeskim:mentions | umls-concept:C0236171 | lld:lifeskim |
| pubmed-article:16449190 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:16449190 | lifeskim:mentions | umls-concept:C1442758 | lld:lifeskim |
| pubmed-article:16449190 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
| pubmed-article:16449190 | lifeskim:mentions | umls-concept:C0392673 | lld:lifeskim |
| pubmed-article:16449190 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
| pubmed-article:16449190 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
| pubmed-article:16449190 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:16449190 | pubmed:dateCreated | 2006-2-1 | lld:pubmed |
| pubmed-article:16449190 | pubmed:abstractText | Mutations in the gene encoding SP-C (surfactant protein C; SFTPC) have been linked to interstitial lung disease (ILD) in children and adults. Expression of the index mutation, SP-C(Deltaexon4), in transiently transfected cells and type II cells of transgenic mice resulted in misfolding of the proprotein, activation of endoplasmic reticulum (ER) stress pathways, and cytotoxicity. In this study, we show that stably transfected cells adapted to chronic ER stress imposed by the constitutive expression of SP-C(Deltaexon4) via an NF-kappaB-dependent pathway. However, the infection of cells expressing SP-C(Deltaexon4) with respiratory syncytial virus resulted in significantly enhanced cytotoxicity associated with accumulation of the mutant proprotein, pronounced activation of the unfolded protein response, and cell death. Adaptation to chronic ER stress imposed by misfolded SP-C was associated with increased susceptibility to viral-induced cell death. The wide variability in the age of onset of ILD in patients with SFTPC mutations may be related to environmental insults that ultimately overwhelm the homeostatic cytoprotective response. | lld:pubmed |
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| pubmed-article:16449190 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16449190 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16449190 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:16449190 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:16449190 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16449190 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:16449190 | pubmed:issn | 0021-9525 | lld:pubmed |
| pubmed-article:16449190 | pubmed:author | pubmed-author:KlosIu SIuS | lld:pubmed |
| pubmed-article:16449190 | pubmed:author | pubmed-author:NaCheng-LunCL | lld:pubmed |
| pubmed-article:16449190 | pubmed:author | pubmed-author:WeaverTimothy... | lld:pubmed |
| pubmed-article:16449190 | pubmed:author | pubmed-author:WongHector... | lld:pubmed |
| pubmed-article:16449190 | pubmed:author | pubmed-author:BridgesJames... | lld:pubmed |
| pubmed-article:16449190 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16449190 | pubmed:day | 30 | lld:pubmed |
| pubmed-article:16449190 | pubmed:volume | 172 | lld:pubmed |
| pubmed-article:16449190 | pubmed:owner | NLM | lld:pubmed |
