TY - JOUR
T1 - Analysis of gene expression in the wound repair/regeneration process
AU - Li, Xinmin
AU - Mohan, Subburaman
AU - Gu, Weikuan
AU - Baylink, David J.
N1 - Mamm Genome. 2001 Jan;12(1):52-9. Comparative Study; Research Support, U.S. Gov't, Non-P.H.S.
PY - 2001
Y1 - 2001
N2 - Wound repair/regeneration is a complex process consisting of three stages: inflammation, tissue regrowth, and remodeling, which together involve the action of hundreds of genes. In order to i) identify and analyze the genes that are expressed at the inflammatory stage of repair (i.e., 24 h after injury) and ii) evaluate the molecular basis of fast-wound repair/regeneration in adult mammals, we examined the expression of 8734 sequence-verified genes in response to ear punch in a fast wound-repair/regeneration strain, MRL/MpJ-FasIpr mice, and a slow-wound-repair strain, C57BL/6J mice. Many differentially expressed genes can be assigned to wound-repairing pathways known to be active during the inflammatory phase, whereas others are involved in pathways not previously associated with wound repair. Many genes of unknown function (ESTs) exhibited a more than twofold increase in MRL/MpJ-FasIpr or C57BL/6J mice, suggesting that current understanding of the molecular events at the inflammatory stage of repair is still limited. A comparison of the differential expression profiles between MRL/MpJ-FasIpr and C57BL/6J mice suggests that fastwound-repair in MRL/MpJ-FasIpr mice is mediated by a metabolic shift toward a low inflammatory response and an enhanced tissue repair.
AB - Wound repair/regeneration is a complex process consisting of three stages: inflammation, tissue regrowth, and remodeling, which together involve the action of hundreds of genes. In order to i) identify and analyze the genes that are expressed at the inflammatory stage of repair (i.e., 24 h after injury) and ii) evaluate the molecular basis of fast-wound repair/regeneration in adult mammals, we examined the expression of 8734 sequence-verified genes in response to ear punch in a fast wound-repair/regeneration strain, MRL/MpJ-FasIpr mice, and a slow-wound-repair strain, C57BL/6J mice. Many differentially expressed genes can be assigned to wound-repairing pathways known to be active during the inflammatory phase, whereas others are involved in pathways not previously associated with wound repair. Many genes of unknown function (ESTs) exhibited a more than twofold increase in MRL/MpJ-FasIpr or C57BL/6J mice, suggesting that current understanding of the molecular events at the inflammatory stage of repair is still limited. A comparison of the differential expression profiles between MRL/MpJ-FasIpr and C57BL/6J mice suggests that fastwound-repair in MRL/MpJ-FasIpr mice is mediated by a metabolic shift toward a low inflammatory response and an enhanced tissue repair.
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U2 - 10.1007/s003350010230
DO - 10.1007/s003350010230
M3 - Article
C2 - 11178744
SN - 0938-8990
VL - 12
SP - 52
EP - 59
JO - Mammalian Genome
JF - Mammalian Genome
IS - 1
ER -