Show simple item record

dc.contributor.authorMarella, Mathieu
dc.contributor.authorSeo, Byoung Boo
dc.contributor.authorFlotte, Terence R.
dc.contributor.authorMatsuno-Yagi, Akemi
dc.contributor.authorYagi, Takao
dc.date2022-08-11T08:10:14.000
dc.date.accessioned2022-08-23T17:00:42Z
dc.date.available2022-08-23T17:00:42Z
dc.date.issued2011-10-03
dc.date.submitted2012-01-17
dc.identifier.citationMarella M, Seo BB, Flotte TR, Matsuno-Yagi A, Yagi T (2011) No Immune Responses by the Expression of the Yeast Ndi1 Protein in Rats. PLoS ONE 6(10): e25910. doi:10.1371/journal.pone.0025910. <a href="http://dx.doi.org/10.1371/journal.pone.0025910">Link to article on publisher's website</a>
dc.identifier.issn1932-6203
dc.identifier.doi10.1371/journal.pone.0025910
dc.identifier.pmid21991386
dc.identifier.urihttp://hdl.handle.net/20.500.14038/43850
dc.description.abstractBACKGROUND: The rotenone-insensitive internal NADH-quinone oxidoreductase from yeast, Ndi1, has been shown to work as a replacement molecule for complex I in the respiratory chain of mammalian mitochondria. In the so-called transkingdom gene therapy, one major concern is the fact that the yeast protein is foreign in mammals. Long term expression of Ndi1 observed in rodents with no apparent damage to the target tissue was indicative of no action by the host's immune system. METHODOLOGY/PRINCIPAL FINDINGS: In the present study, we examined rat skeletal muscles expressing Ndi1 for possible signs of inflammatory or immune response. In parallel, we carried out delivery of the GFP gene using the same viral vector that was used for the NDI1 gene. The tissues were subjected to H&E staining and immunohistochemical analyses using antibodies specific for markers, CD11b, CD3, CD4, and CD8. The data showed no detectable signs of an immune response with the tissues expressing Ndi1. In contrast, mild but distinctive positive reactions were observed in the tissues expressing GFP. This clear difference most likely comes from the difference in the location of the expressed protein. Ndi1 was localized to the mitochondria whereas GFP was in the cytosol. CONCLUSIONS/SIGNIFICANCE: We demonstrated that Ndi1 expression did not trigger any inflammatory or immune response in rats. These results push forward the Ndi1-based molecular therapy and also expand the possibility of using foreign proteins that are directed to subcellular organelle such as mitochondria.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=21991386&dopt=Abstract">Link to article in PubMed</a>
dc.rights<p>Copyright: © 2011 Marella et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</p>
dc.subjectSaccharomyces cerevisiae Proteins
dc.subjectElectron Transport Complex I
dc.subjectImmunity
dc.subjectGene Therapy
dc.subjectAllergy and Immunology
dc.subjectGenetics and Genomics
dc.subjectImmunology and Infectious Disease
dc.subjectPediatrics
dc.titleNo immune responses by the expression of the yeast Ndi1 protein in rats
dc.typeJournal Article
dc.source.journaltitlePLoS One
dc.source.volume6
dc.source.issue10
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1062&amp;context=peds_pulmonary&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/peds_pulmonary/62
dc.identifier.contextkey2451746
refterms.dateFOA2022-08-23T17:00:43Z
html.description.abstract<p>BACKGROUND: The rotenone-insensitive internal NADH-quinone oxidoreductase from yeast, Ndi1, has been shown to work as a replacement molecule for complex I in the respiratory chain of mammalian mitochondria. In the so-called transkingdom gene therapy, one major concern is the fact that the yeast protein is foreign in mammals. Long term expression of Ndi1 observed in rodents with no apparent damage to the target tissue was indicative of no action by the host's immune system.</p> <p>METHODOLOGY/PRINCIPAL FINDINGS: In the present study, we examined rat skeletal muscles expressing Ndi1 for possible signs of inflammatory or immune response. In parallel, we carried out delivery of the GFP gene using the same viral vector that was used for the NDI1 gene. The tissues were subjected to H&E staining and immunohistochemical analyses using antibodies specific for markers, CD11b, CD3, CD4, and CD8. The data showed no detectable signs of an immune response with the tissues expressing Ndi1. In contrast, mild but distinctive positive reactions were observed in the tissues expressing GFP. This clear difference most likely comes from the difference in the location of the expressed protein. Ndi1 was localized to the mitochondria whereas GFP was in the cytosol.</p> <p>CONCLUSIONS/SIGNIFICANCE: We demonstrated that Ndi1 expression did not trigger any inflammatory or immune response in rats. These results push forward the Ndi1-based molecular therapy and also expand the possibility of using foreign proteins that are directed to subcellular organelle such as mitochondria.</p>
dc.identifier.submissionpathpeds_pulmonary/62
dc.contributor.departmentGene Therapy Center
dc.contributor.departmentDepartment of Pediatrics
dc.source.pagese25910


Files in this item

Thumbnail
Name:
journal.pone.0025910.pdf
Size:
1.135Mb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record