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 |
Published |
Boston
Springer US
01.10.2011
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | 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. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0360-3997 1573-2576 |
DOI: | 10.1007/s10753-010-9235-y |