Distinct Early Inflammatory Events during Ear Tissue Regeneration in Mice Selected for High Inflammation Bearing Slc11a1 R and S Alleles

High inflammatory AIRmax mice homozygous for Slc11a1 R and S alleles were produced. AIRmax SS mice showed faster ear tissue regeneration than AIRmax RR mice, suggesting that the S allele favored tissue restoration. Here, we investigated the gene expression profiles and the inflammatory reactions of...

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Published inInflammation Vol. 34; no. 5; pp. 303 - 313
Main Authors Canhamero, Tatiane, Reines, Brandon, Peters, Luciana C., Borrego, Andrea, Carneiro, Patricia S., Albuquerque, Layra L., Cabrera, Wafa H., Ribeiro, Orlando G., Jensen, Jose R., Starobinas, Nancy, Ibañez, Olga M., De Franco, Marcelo
Format Journal Article
LanguageEnglish
Published Boston Springer US 01.10.2011
Springer Nature B.V
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Abstract High inflammatory AIRmax mice homozygous for Slc11a1 R and S alleles were produced. AIRmax SS mice showed faster ear tissue regeneration than AIRmax RR mice, suggesting that the S allele favored tissue restoration. Here, we investigated the gene expression profiles and the inflammatory reactions of AIRmax RR and AIRmax SS mice during the initial phase of ear tissue regeneration. We observed superior levels of analysis of wound myeloperoxidase and edema in AIRmax SS mice, although similar cell influx was verified in both lines. Of the genes, 794 were up- and 674 down-regulated in AIRmax RR , while 735 genes were found to be up- and 1616 down-regulated in AIRmax SS mice 48 h after punch. Both mouse lines showed significant over-represented genes related to cell proliferation; however AIRmax SS displayed up-regulation of inflammatory response genes. Quantitative PCR experiments showed higher expressions of Tgfb1 , Dap12 and Trem1 genes in AIRmax SS mice. These results indicate that Slc11a1 gene modulated the early inflammatory events of ear tissue regeneration.
AbstractList High inflammatory AIRmax mice homozygous for Slc11a1 R and S alleles were produced. AIRmax^sup SS^ mice showed faster ear tissue regeneration than AIRmax^sup RR^ mice, suggesting that the S allele favored tissue restoration. Here, we investigated the gene expression profiles and the inflammatory reactions of AIRmax^sup RR^ and AIRmax^sup SS^ mice during the initial phase of ear tissue regeneration. We observed superior levels of analysis of wound myeloperoxidase and edema in AIRmax^sup SS^ mice, although similar cell influx was verified in both lines. Of the genes, 794 were up- and 674 down-regulated in AIRmax^sup RR^, while 735 genes were found to be up- and 1616 down-regulated in AIRmax^sup SS^ mice 48 h after punch. Both mouse lines showed significant over-represented genes related to cell proliferation; however AIRmax^sup SS^ displayed up-regulation of inflammatory response genes. Quantitative PCR experiments showed higher expressions of Tgfb1, Dap12 and Trem1 genes in AIRmax^sup SS^ mice. These results indicate that Slc11a1 gene modulated the early inflammatory events of ear tissue regeneration.[PUBLICATION ABSTRACT]
High inflammatory AIRmax mice homozygous for Slc11a1 R and S alleles were produced. AIRmax super(SS) mice showed faster ear tissue regeneration than AIRmax super(RR) mice, suggesting that the S allele favored tissue restoration. Here, we investigated the gene expression profiles and the inflammatory reactions of AIRmax super(RR) and AIRmax super(SS) mice during the initial phase of ear tissue regeneration. We observed superior levels of analysis of wound myeloperoxidase and edema in AIRmax super(SS) mice, although similar cell influx was verified in both lines. Of the genes, 794 were up- and 674 down-regulated in AIRmax super(RR), while 735 genes were found to be up- and 1616 down-regulated in AIRmax super(SS) mice 48 h after punch. Both mouse lines showed significant over-represented genes related to cell proliferation; however AIRmax super(SS) displayed up-regulation of inflammatory response genes. Quantitative PCR experiments showed higher expressions of Tgfb1, Dap12 and Trem1 genes in AIRmax super( SS) mice. These results indicate that Slc11a1 gene modulated the early inflammatory events of ear tissue regeneration.
High inflammatory AIRmax mice homozygous for Slc11a1 R and S alleles were produced. AIRmax SS mice showed faster ear tissue regeneration than AIRmax RR mice, suggesting that the S allele favored tissue restoration. Here, we investigated the gene expression profiles and the inflammatory reactions of AIRmax RR and AIRmax SS mice during the initial phase of ear tissue regeneration. We observed superior levels of analysis of wound myeloperoxidase and edema in AIRmax SS mice, although similar cell influx was verified in both lines. Of the genes, 794 were up- and 674 down-regulated in AIRmax RR , while 735 genes were found to be up- and 1616 down-regulated in AIRmax SS mice 48 h after punch. Both mouse lines showed significant over-represented genes related to cell proliferation; however AIRmax SS displayed up-regulation of inflammatory response genes. Quantitative PCR experiments showed higher expressions of Tgfb1 , Dap12 and Trem1 genes in AIRmax SS mice. These results indicate that Slc11a1 gene modulated the early inflammatory events of ear tissue regeneration.
High inflammatory AIRmax mice homozygous for Slc11a1 R and S alleles were produced. AIRmax(SS) mice showed faster ear tissue regeneration than AIRmax(RR) mice, suggesting that the S allele favored tissue restoration. Here, we investigated the gene expression profiles and the inflammatory reactions of AIRmax(RR) and AIRmax(SS) mice during the initial phase of ear tissue regeneration. We observed superior levels of analysis of wound myeloperoxidase and edema in AIRmax(SS) mice, although similar cell influx was verified in both lines. Of the genes, 794 were up- and 674 down-regulated in AIRmax(RR), while 735 genes were found to be up- and 1616 down-regulated in AIRmax(SS) mice 48 h after punch. Both mouse lines showed significant over-represented genes related to cell proliferation; however AIRmax(SS) displayed up-regulation of inflammatory response genes. Quantitative PCR experiments showed higher expressions of Tgfb1, Dap12 and Trem1 genes in AIRmax(SS) mice. These results indicate that Slc11a1 gene modulated the early inflammatory events of ear tissue regeneration.
Author De Franco, Marcelo
Ribeiro, Orlando G.
Ibañez, Olga M.
Canhamero, Tatiane
Reines, Brandon
Carneiro, Patricia S.
Starobinas, Nancy
Peters, Luciana C.
Albuquerque, Layra L.
Jensen, Jose R.
Borrego, Andrea
Cabrera, Wafa H.
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ear regeneration
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Snippet High inflammatory AIRmax mice homozygous for Slc11a1 R and S alleles were produced. AIRmax SS mice showed faster ear tissue regeneration than AIRmax RR mice,...
High inflammatory AIRmax mice homozygous for Slc11a1 R and S alleles were produced. AIRmax(SS) mice showed faster ear tissue regeneration than AIRmax(RR) mice,...
High inflammatory AIRmax mice homozygous for Slc11a1 R and S alleles were produced. AIRmax^sup SS^ mice showed faster ear tissue regeneration than AIRmax^sup...
High inflammatory AIRmax mice homozygous for Slc11a1 R and S alleles were produced. AIRmax super(SS) mice showed faster ear tissue regeneration than AIRmax...
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springer
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Index Database
Publisher
StartPage 303
SubjectTerms Alleles
Animals
Base Sequence
Biomedical and Life Sciences
Biomedicine
Cation Transport Proteins - genetics
Cation Transport Proteins - physiology
DNA Primers - genetics
Ear, External - injuries
Ear, External - physiology
Female
Gene Expression
Immunology
Inflammation - genetics
Inflammation - physiopathology
Internal Medicine
Male
Mice
Mice, Inbred Strains
Pathology
Peroxidase - metabolism
Pharmacology/Toxicology
Quantitative Trait Loci
Real-Time Polymerase Chain Reaction
Regeneration - genetics
Regeneration - physiology
Rheumatology
Wound Healing - genetics
Wound Healing - physiology
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Title Distinct Early Inflammatory Events during Ear Tissue Regeneration in Mice Selected for High Inflammation Bearing Slc11a1 R and S Alleles
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