Interferon-Gamma (IFN-γ)-Mediated Retinal Ganglion Cell Death in Human Tyrosinase T Cell Receptor Transgenic Mouse
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{"title"=>"Interferon-gamma (IFN-γ)-mediated retinal ganglion cell death in human tyrosinase t cell receptor transgenic mouse", "type"=>"journal", "authors"=>[{"first_name"=>"Shahid", "last_name"=>"Husain", "scopus_author_id"=>"36351753800"}, {"first_name"=>"Yasir", "last_name"=>"Abdul", "scopus_author_id"=>"55358881300"}, {"first_name"=>"Christine", "last_name"=>"Webster", "scopus_author_id"=>"56074583700"}, {"first_name"=>"Shilpak", "last_name"=>"Chatterjee", "scopus_author_id"=>"56661161400"}, {"first_name"=>"Pravin", "last_name"=>"Kesarwani", "scopus_author_id"=>"24344127700"}, {"first_name"=>"Shikhar", "last_name"=>"Mehrotra", "scopus_author_id"=>"7102264246"}], "year"=>2014, "source"=>"PLoS ONE", "identifiers"=>{"issn"=>"19326203", "pui"=>"372643368", "doi"=>"10.1371/journal.pone.0089392", "sgr"=>"84896541209", "scopus"=>"2-s2.0-84896541209"}, "id"=>"f4c02722-c671-3925-935a-10e6fe388f30", "link"=>"http://www.mendeley.com/research/interferongamma-ifn%CE%B3mediated-retinal-ganglion-cell-death-human-tyrosinase-t-cell-receptor-transgenic-1", "reader_count"=>2, "reader_count_by_academic_status"=>{"Unspecified"=>1, "Student > Ph. D. Student"=>1}, "reader_count_by_user_role"=>{"Unspecified"=>1, "Student > Ph. D. Student"=>1}, "reader_count_by_subject_area"=>{"Unspecified"=>1, "Medicine and Dentistry"=>1}, "reader_count_by_subdiscipline"=>{"Medicine and Dentistry"=>{"Medicine and Dentistry"=>1}, "Unspecified"=>{"Unspecified"=>1}}, "group_count"=>0}

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Figshare

  • {"files"=>["https://ndownloader.figshare.com/files/1404705"], "description"=>"<p>(<b>A</b>) h3T-A2 mouse with spontaneous vitiligo. Double-transgenic h3T-A2 mouse along with non-transgenic littermate at 18 months-of-age. Development of spontaneous progressive vitiligo in double-transgenic mouse on extreme left is noticeable after five weeks-of-age. Age-matched h3T-A2 mouse shows de-pigmentation. (<b>B</b>) Pattern-ERG recording in 12-month-old wild-type HLA-A2 and h3T-A2 mice. Each waveform is a mean of 300 individual waveforms taken at an interval of 1 second for each data point. Data are mean ±SE; *<i>p</i><0.05; n = 6–7. (<b>C</b>) Fluorescence micrographs of flat-mounted retinas depicting Fluorogold-labeled retina ganglion cells (RGCs) in 12-month-old wild-type HLA-A2 and h3T-A2 mice. Briefly, 2 µL of a 5% solution of fluorogold was injected into the superior colliculus of anesthetized animals. Seven days post injection, animals were euthanized and retinas were prepared as flat-mounts, vitreous-side facing up. Fluorescent RGCs were visualized under Zeiss microscopy. (<b>D</b>) RGCs were counted in 8 microscopic fields of identical size (150 µm<sup>2</sup> area) for each retina using Image J software. *<i>p</i><0.05; n = 6 for each group.</p>", "links"=>[], "tags"=>["Anatomy and physiology", "Immune physiology", "cytokines", "Ocular system", "Biochemistry", "biotechnology", "Genetic engineering", "transgenics", "immunology", "Immune cells", "t cells", "Model organisms", "Animal models", "mouse", "Molecular cell biology", "Signal transduction", "Signaling in cellular processes", "Cell death", "ophthalmology", "glaucoma", "Retinal disorders"], "article_id"=>949613, "categories"=>["Biological Sciences", "Medicine"], "users"=>["Shahid Husain", "Yasir Abdul", "Christine Webster", "Shilpak Chatterjee", "Pravin Kesarwani", "Shikhar Mehrotra"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0089392.g001", "stats"=>{"downloads"=>0, "page_views"=>11, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Figure_1_/949613", "title"=>"Figure 1", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2014-02-28 04:45:46"}
  • {"files"=>["https://ndownloader.figshare.com/files/1404713"], "description"=>"<p>Band intensities of Western blots were quantitated by densitometry. Data are mean ±SE, *<i>p</i><0.05; n = 3.</p>", "links"=>[], "tags"=>["Anatomy and physiology", "Immune physiology", "cytokines", "Ocular system", "Biochemistry", "biotechnology", "Genetic engineering", "transgenics", "immunology", "Immune cells", "t cells", "Model organisms", "Animal models", "mouse", "Molecular cell biology", "Signal transduction", "Signaling in cellular processes", "Cell death", "ophthalmology", "glaucoma", "Retinal disorders", "optic", "nerves", "12-month-old", "hla-a2", "h3t-a2", "mice", "removed", "blotting"], "article_id"=>949621, "categories"=>["Biological Sciences", "Medicine"], "users"=>["Shahid Husain", "Yasir Abdul", "Christine Webster", "Shilpak Chatterjee", "Pravin Kesarwani", "Shikhar Mehrotra"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0089392.g009", "stats"=>{"downloads"=>0, "page_views"=>17, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_The_optic_nerves_of_12_month_old_HLA_A2_and_h3T_A2_mice_were_removed_and_analyzed_by_Western_blotting_using_anti_IFN_947_antibodies_/949621", "title"=>"The optic nerves of 12-month-old HLA-A2 and h3T-A2 mice were removed and analyzed by Western blotting using anti-IFN-γ antibodies.", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2014-02-28 04:45:46"}
  • {"files"=>["https://ndownloader.figshare.com/files/1404712"], "description"=>"<p>Band intensities of Western blots were quantitated by densitometry. Data are mean ±SE, *<i>p</i><0.05; n = 4–7 for HLA-A2 and h3T-A2 groups. (C) Retina cryosections of 12-month-old HLA-A2 and h3T-A2 mice were immunostained by anti-caspase-3 antibodies (green), anti-GFAP (red), and nuclei were stained with Dapi (blue). There was no positive staining when primary antibodies were omitted (not shown). Bar size is 20 µm. Data are a representation of at least four independent experiments.</p>", "links"=>[], "tags"=>["Anatomy and physiology", "Immune physiology", "cytokines", "Ocular system", "Biochemistry", "biotechnology", "Genetic engineering", "transgenics", "immunology", "Immune cells", "t cells", "Model organisms", "Animal models", "mouse", "Molecular cell biology", "Signal transduction", "Signaling in cellular processes", "Cell death", "ophthalmology", "glaucoma", "Retinal disorders", "12-month-old", "hla-a2", "h3t-a2", "mice", "enucleated", "retina", "extracts", "blotting", "anti-caspase-9", "anti-caspase-3"], "article_id"=>949620, "categories"=>["Biological Sciences", "Medicine"], "users"=>["Shahid Husain", "Yasir Abdul", "Christine Webster", "Shilpak Chatterjee", "Pravin Kesarwani", "Shikhar Mehrotra"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0089392.g008", "stats"=>{"downloads"=>2, "page_views"=>89, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Eyes_of_12_month_old_HLA_A2_and_h3T_A2_mice_were_enucleated_and_whole_retina_extracts_were_analyzed_by_Western_blotting_using_anti_caspase_9_A_or_anti_caspase_3_B_antibodies_/949620", "title"=>"Eyes of 12-month-old HLA-A2 and h3T-A2 mice were enucleated and whole retina extracts were analyzed by Western blotting using anti-caspase-9 (A) or anti-caspase-3 (B) antibodies.", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2014-02-28 04:45:46"}
  • {"files"=>["https://ndownloader.figshare.com/files/1404709"], "description"=>"<p>(<b>A</b>) Eyes of 12-month-old HLA-A2 and H3TA2 mice were enucleated and whole retinal extracts were analyzed by Western blotting using anti-IFN-γ antibodies. Band intensities of Western blots were quantitated by densitometry. Data are mean ±SE. *<i>p</i><0.05; n = 11 for HLA-A2 and h3T-A2 groups. (<b>B)</b> Retinal cryosections of 12-month-old HLA-A2 and H3TA2 mice were immunostained by anti-IFN-γ (green) antibodies and nuclei were stained with DAPI (blue). There was no positive staining when primary antibodies were omitted (not shown). Bar size is 20 microns. Data is a representation of at least four independent experiments.</p>", "links"=>[], "tags"=>["Anatomy and physiology", "Immune physiology", "cytokines", "Ocular system", "Biochemistry", "biotechnology", "Genetic engineering", "transgenics", "immunology", "Immune cells", "t cells", "Model organisms", "Animal models", "mouse", "Molecular cell biology", "Signal transduction", "Signaling in cellular processes", "Cell death", "ophthalmology", "glaucoma", "Retinal disorders"], "article_id"=>949617, "categories"=>["Biological Sciences", "Medicine"], "users"=>["Shahid Husain", "Yasir Abdul", "Christine Webster", "Shilpak Chatterjee", "Pravin Kesarwani", "Shikhar Mehrotra"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0089392.g005", "stats"=>{"downloads"=>0, "page_views"=>10, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Figure_5_/949617", "title"=>"Figure 5", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2014-02-28 04:45:46"}
  • {"files"=>["https://ndownloader.figshare.com/files/1404707"], "description"=>"<p>Representative photomicrographs comparing morphologic changes in the 12-month-old wild-type HLA-A2 and h3T-A2 transgenic mice. Retina sections were stained with hematoxylin and eosin.</p>", "links"=>[], "tags"=>["Anatomy and physiology", "Immune physiology", "cytokines", "Ocular system", "Biochemistry", "biotechnology", "Genetic engineering", "transgenics", "immunology", "Immune cells", "t cells", "Model organisms", "Animal models", "mouse", "Molecular cell biology", "Signal transduction", "Signaling in cellular processes", "Cell death", "ophthalmology", "glaucoma", "Retinal disorders", "retina", "h3t-a2", "transgenic"], "article_id"=>949615, "categories"=>["Biological Sciences", "Medicine"], "users"=>["Shahid Husain", "Yasir Abdul", "Christine Webster", "Shilpak Chatterjee", "Pravin Kesarwani", "Shikhar Mehrotra"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0089392.g003", "stats"=>{"downloads"=>0, "page_views"=>35, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Morphological_evidence_of_retina_damage_in_h3T_A2_transgenic_mice_/949615", "title"=>"Morphological evidence of retina damage in h3T-A2 transgenic mice.", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2014-02-28 04:45:46"}
  • {"files"=>["https://ndownloader.figshare.com/files/1404708"], "description"=>"<p>(<b>A</b>) Control mouse and h3T-A2 mice on deficient backgrounds as indicated. White arrows point to de-pigmentation of ear pinna and tails observed in these h3T-A2 pups at time of weaning (day 21). (<b>B</b>) Splenocytes (n = 4) from age matched (8 weeks) effector molecules competent (h3TA2) or deficient (h3T-A2IFN-γ<sup>-/-</sup>, h3T-A2TNF-α<sup>-/-</sup> and h3TA2Perforin<sup>-/-</sup>) mice were co-cultured overnight with cognate antigen h-Tyr (1 µg/ml) or control peptide (MART-1 at 1 µg/ml) pulsed surrogate antigen presenting T2-A2 cells. Supernatant were collected and analyzed for cytokine release by ELISA as per manufacturer's protocol.</p>", "links"=>[], "tags"=>["Anatomy and physiology", "Immune physiology", "cytokines", "Ocular system", "Biochemistry", "biotechnology", "Genetic engineering", "transgenics", "immunology", "Immune cells", "t cells", "Model organisms", "Animal models", "mouse", "Molecular cell biology", "Signal transduction", "Signaling in cellular processes", "Cell death", "ophthalmology", "glaucoma", "Retinal disorders"], "article_id"=>949616, "categories"=>["Biological Sciences", "Medicine"], "users"=>["Shahid Husain", "Yasir Abdul", "Christine Webster", "Shilpak Chatterjee", "Pravin Kesarwani", "Shikhar Mehrotra"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0089392.g004", "stats"=>{"downloads"=>0, "page_views"=>7, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Figure_4_/949616", "title"=>"Figure 4", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2014-02-28 04:45:46"}
  • {"files"=>["https://ndownloader.figshare.com/files/1404706"], "description"=>"<p>Data are expressed as mean ±SE. *<i>p</i><0.05; n = 6 for each group. Bar size is 20 µm. Arrows indicate CD3 staining; arrowheads indicate non-selective staining, as also observed in the negative control (not shown).</p>", "links"=>[], "tags"=>["Anatomy and physiology", "Immune physiology", "cytokines", "Ocular system", "Biochemistry", "biotechnology", "Genetic engineering", "transgenics", "immunology", "Immune cells", "t cells", "Model organisms", "Animal models", "mouse", "Molecular cell biology", "Signal transduction", "Signaling in cellular processes", "Cell death", "ophthalmology", "glaucoma", "Retinal disorders", "retina", "12-month-old", "wild-type", "hla-a2", "h3t-a2", "mice", "blotting", "immunohistochemistry"], "article_id"=>949614, "categories"=>["Biological Sciences", "Medicine"], "users"=>["Shahid Husain", "Yasir Abdul", "Christine Webster", "Shilpak Chatterjee", "Pravin Kesarwani", "Shikhar Mehrotra"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0089392.g002", "stats"=>{"downloads"=>0, "page_views"=>13, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Detection_of_CD3_in_the_retina_of_12_month_old_wild_type_HLA_A2_and_h3T_A2_mice_by_Western_blotting_A_and_immunohistochemistry_B_/949614", "title"=>"Detection of CD3+ in the retina of 12-month-old wild-type HLA-A2 and h3T-A2 mice by Western blotting (A) and immunohistochemistry (B).", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2014-02-28 04:45:46"}
  • {"files"=>["https://ndownloader.figshare.com/files/1404714"], "description"=>"<p>Values are (mean ±SE), n = 3–4. Values were compared between groups using one-way ANOVA with Dunnett's post-test.</p><p>*indicates significant difference from wild-type eye (<i>p</i><0.05). NFL, nerve fiber layer; IPL, inner plexiform layer; INL, inner nuclear layer; OPL, outer plexiform layer; ONL, outer nuclear layer.</p>", "links"=>[], "tags"=>["Anatomy and physiology", "Immune physiology", "cytokines", "Ocular system", "Biochemistry", "biotechnology", "Genetic engineering", "transgenics", "immunology", "Immune cells", "t cells", "Model organisms", "Animal models", "mouse", "Molecular cell biology", "Signal transduction", "Signaling in cellular processes", "Cell death", "ophthalmology", "glaucoma", "Retinal disorders", "retina", "layers", "12-month-old", "wild-type", "hla-a2", "h3t-a2", "transgenic"], "article_id"=>949622, "categories"=>["Biological Sciences", "Medicine"], "users"=>["Shahid Husain", "Yasir Abdul", "Christine Webster", "Shilpak Chatterjee", "Pravin Kesarwani", "Shikhar Mehrotra"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0089392.t001", "stats"=>{"downloads"=>3, "page_views"=>29, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Thickness_of_retina_and_individual_layers_measured_in_12_month_old_wild_type_HLA_A2_and_h3T_A2_transgenic_mice_/949622", "title"=>"Thickness of retina and individual layers measured in 12-month-old wild-type HLA-A2 and h3T-A2 transgenic mice.", "pos_in_sequence"=>0, "defined_type"=>3, "published_date"=>"2014-02-28 04:45:46"}
  • {"files"=>["https://ndownloader.figshare.com/files/1404711"], "description"=>"<p>Green color indicates staining for GFAP and blue for DAPI in the nuclei. There was no positive staining when primary antibodies were omitted (not shown). Fluorescence microscopy; bar size is 20 µm.</p>", "links"=>[], "tags"=>["Anatomy and physiology", "Immune physiology", "cytokines", "Ocular system", "Biochemistry", "biotechnology", "Genetic engineering", "transgenics", "immunology", "Immune cells", "t cells", "Model organisms", "Animal models", "mouse", "Molecular cell biology", "Signal transduction", "Signaling in cellular processes", "Cell death", "ophthalmology", "glaucoma", "Retinal disorders", "12-month-old", "wild-type", "hla-a2", "h3t-a2", "mice", "enucleated", "cryosections", "immunostained", "anti-gfap"], "article_id"=>949619, "categories"=>["Biological Sciences", "Medicine"], "users"=>["Shahid Husain", "Yasir Abdul", "Christine Webster", "Shilpak Chatterjee", "Pravin Kesarwani", "Shikhar Mehrotra"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0089392.g007", "stats"=>{"downloads"=>1, "page_views"=>33, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Eyes_of_12_month_old_wild_type_HLA_A2_and_h3T_A2_mice_were_enucleated_and_cryosections_were_immunostained_by_anti_GFAP_antibodies_/949619", "title"=>"Eyes of 12-month-old wild-type HLA-A2 and h3T-A2 mice were enucleated and cryosections were immunostained by anti-GFAP antibodies.", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2014-02-28 04:45:46"}
  • {"files"=>["https://ndownloader.figshare.com/files/1404710"], "description"=>"<p>There was no positive staining when primary antibodies were omitted (not shown). Fluorescence microscopy; bar size is 20 µm.</p>", "links"=>[], "tags"=>["Anatomy and physiology", "Immune physiology", "cytokines", "Ocular system", "Biochemistry", "biotechnology", "Genetic engineering", "transgenics", "immunology", "Immune cells", "t cells", "Model organisms", "Animal models", "mouse", "Molecular cell biology", "Signal transduction", "Signaling in cellular processes", "Cell death", "ophthalmology", "glaucoma", "Retinal disorders", "12-month-old", "wild-type", "hla-a2", "h3t-a2", "mice", "enucleated", "cryosections", "immunostained", "anti-gfap", "dapi"], "article_id"=>949618, "categories"=>["Biological Sciences", "Medicine"], "users"=>["Shahid Husain", "Yasir Abdul", "Christine Webster", "Shilpak Chatterjee", "Pravin Kesarwani", "Shikhar Mehrotra"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0089392.g006", "stats"=>{"downloads"=>0, "page_views"=>18, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Eyes_of_12_month_old_wild_type_HLA_A2_and_h3T_A2_mice_were_enucleated_and_cryosections_were_immunostained_by_IFN_947_green_anti_GFAP_red_antibodies_and_blue_for_DAPI_in_the_nuclei_/949618", "title"=>"Eyes of 12-month-old wild-type HLA-A2 and h3T-A2 mice were enucleated and cryosections were immunostained by IFN-γ (green), anti-GFAP (red) antibodies, and blue for DAPI in the nuclei.", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2014-02-28 04:45:46"}

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Relative Metric

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