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 in | Inflammation Vol. 34; no. 5; pp. 303 - 313 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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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. |
Author_xml | – sequence: 1 givenname: Tatiane surname: Canhamero fullname: Canhamero, Tatiane organization: Laboratório de Imunogenética, Instituto Butantan – sequence: 2 givenname: Brandon surname: Reines fullname: Reines, Brandon organization: Ghost Lab, Laboratory of Cellular and Molecular Immunology, NIAID, NIH – sequence: 3 givenname: Luciana C. surname: Peters fullname: Peters, Luciana C. organization: Laboratório de Imunogenética, Instituto Butantan – sequence: 4 givenname: Andrea surname: Borrego fullname: Borrego, Andrea organization: Laboratório de Imunogenética, Instituto Butantan – sequence: 5 givenname: Patricia S. surname: Carneiro fullname: Carneiro, Patricia S. organization: Laboratório de Imunogenética, Instituto Butantan – sequence: 6 givenname: Layra L. surname: Albuquerque fullname: Albuquerque, Layra L. organization: Laboratório de Imunogenética, Instituto Butantan – sequence: 7 givenname: Wafa H. surname: Cabrera fullname: Cabrera, Wafa H. organization: Laboratório de Imunogenética, Instituto Butantan – sequence: 8 givenname: Orlando G. surname: Ribeiro fullname: Ribeiro, Orlando G. organization: Laboratório de Imunogenética, Instituto Butantan – sequence: 9 givenname: Jose R. surname: Jensen fullname: Jensen, Jose R. organization: Laboratório de Imunogenética, Instituto Butantan – sequence: 10 givenname: Nancy surname: Starobinas fullname: Starobinas, Nancy organization: Laboratório de Imunogenética, Instituto Butantan – sequence: 11 givenname: Olga M. surname: Ibañez fullname: Ibañez, Olga M. organization: Laboratório de Imunogenética, Instituto Butantan – sequence: 12 givenname: Marcelo surname: De Franco fullname: De Franco, Marcelo email: mdfranco@butantan.gov.br organization: Laboratório de Imunogenética, Instituto Butantan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/20665098$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_cyto_2018_11_027 crossref_primary_10_1155_2022_3298542 crossref_primary_10_1371_journal_pgen_1007390 crossref_primary_10_1039_c2mt20156a crossref_primary_10_1371_journal_pone_0196230 crossref_primary_10_1038_s41435_023_00199_7 crossref_primary_10_1089_wound_2013_0494 |
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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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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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