| dc.contributor.author | Li, Na | |
| dc.contributor.author | Yin, Lu | |
| dc.contributor.author | Thevenin, Damien | |
| dc.contributor.author | Yamada, Yoshiyuki | |
| dc.contributor.author | Limmon, Gino V. | |
| dc.contributor.author | Chen, Jianzhu | |
| dc.contributor.author | Chow, Vincent T. K. | |
| dc.contributor.author | Engelman, Donald M. | |
| dc.contributor.author | Engelward, Bevin P. | |
| dc.date.accessioned | 2013-03-15T16:16:51Z | |
| dc.date.available | 2013-03-15T16:16:51Z | |
| dc.date.issued | 2013-02 | |
| dc.identifier.issn | 1746-0913 | |
| dc.identifier.issn | 1746-0921 | |
| dc.identifier.uri | http://hdl.handle.net/1721.1/77907 | |
| dc.description.abstract | In this study, we investigate whether pH (low) insertion peptide (pHLIP) can target regions of lung injury associated with influenza infection. Materials & methods: Fluorophore-conjugated pHLIP was injected intraperitoneally into mice infected with a sublethal dose of H1N1 influenza and visualized histologically. Results: pHLIP specifically targeted inflamed lung tissues of infected mice in the later stages of disease and at sites where alveolar type I and type II cells were depleted. Regions of pHLIP-targeted lung tissue were devoid of peroxiredoxin 6, the lung-abundant antioxidant enzyme, and were deficient in pneumocytes. Interestingly, a pHLIP variant possessing mutations that render it insensitive to pH changes was also able to target damaged lung tissue. Conclusion: pHLIP holds potential for delivering therapeutics for lung injury during influenza infection. Furthermore, there may be more than one mechanism that enables pHLIP variants to target inflamed lung tissue. | en_US |
| dc.description.sponsorship | National Institute of Environmental Health Sciences (P01 - ES006052) | en_US |
| dc.description.sponsorship | Singapore–MIT Alliance for Research and Technology | en_US |
| dc.description.sponsorship | National Institutes of Health (U.S.) (grant GM073857) | en_US |
| dc.language.iso | en_US | |
| dc.publisher | Future Medicine | en_US |
| dc.relation.isversionof | http://dx.doi.org/10.2217/fmb.12.134 | en_US |
| dc.rights | Creative Commons Attribution-Noncommercial-Share Alike 3.0 | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/3.0/ | en_US |
| dc.source | Prof. Engelward via Howard | en_US |
| dc.title | Peptide targeting and imaging of damaged lung tissue in influenza-infected mice | en_US |
| dc.type | Article | en_US |
| dc.identifier.citation | Li, Na et al. “Peptide Targeting and Imaging of Damaged Lung Tissue in Influenza-infected Mice.” Future Microbiology 8.2 (2013): 257–269. CrossRef. Web. | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Biological Engineering | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Biology | en_US |
| dc.contributor.department | Singapore-MIT Alliance in Research and Technology (SMART) | en_US |
| dc.contributor.department | Koch Institute for Integrative Cancer Research at MIT | en_US |
| dc.contributor.approver | Engelward, Bevin P. | |
| dc.contributor.mitauthor | Engelward, Bevin P. | |
| dc.contributor.mitauthor | Li, Na | |
| dc.contributor.mitauthor | Yin, Lu | |
| dc.contributor.mitauthor | Yamada, Yoshiyuki | |
| dc.contributor.mitauthor | Chen, Jianzhu | |
| dc.contributor.mitauthor | Limmon, Gino V. | |
| dc.relation.journal | Future Microbiology | en_US |
| dc.eprint.version | Author's final manuscript | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dspace.orderedauthors | Li, Na; Yin, Lu; Thévenin, Damien; Yamada, Yoshiyuki; Limmon, Gino; Chen, Jianzhu; Chow, Vincent TK; Engelman, Donald M; Engelward, Bevin P | en |
| dc.identifier.orcid | https://orcid.org/0000-0002-5687-6154 | |
| dspace.mitauthor.error | true | |
| mit.license | OPEN_ACCESS_POLICY | en_US |
| mit.metadata.status | Complete | |