Increased expressions and activations of apoptosis-related factors in cell signaling during incised skin wound healing in mice: a preliminary study for forensic wound age estimation

Leg Med (Tokyo). 2009 Apr:11 Suppl 1:S155-60. doi: 10.1016/j.legalmed.2009.02.023. Epub 2009 Mar 17.

Abstract

Recent studies have demonstrated that apoptosis plays a pivotal role during skin wound healing and apoptosis-related factors in cell signaling regulate a variety of cellular function. In this study, the expressions of p38MAPK, and JNK, iNOS, eNOS were detected and the activations of caspase-6, -7, -8, -9, and calpain, another signaling pathway of apoptosis, were also investigated by immunohistochemical staining and Western blotting in mice. A time-dependent increase of each protein level was observed by immunohistochemistry and Western blot in mouse skin incision. p38MAPK level peaked at 12 h and 3 d, calpain level peaked at 1 d and 5 d, iNOS level peaked at 1 d and 10 d, while the peak levels of eNOS, caspase-6, -7, -8, and -9 occurred at 3 d and p-JNK at 1 d post-injury. In the early phase of wound healing, infiltrating polymorphonulcear cells were labeled with all the factors except caspase-8. Thereafter, infiltrating mononuclear cells and proliferating spindle-shaped fibroblastic cells showed positive staining for p38MAPK, JNK, calpain, caspases and NOS. The activation of caspase-8, -9, -6, and -7 as detected by Western blot indicated that caspase apoptotic pathway may take effect in cellular elimination during skin wound healing. From the viewpoint of forensic pathology, the time-dependent expressions of the factors in apoptotic pathway during skin incised wound healing may be used as potential markers for wound age estimation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Calpain / metabolism
  • Caspases / metabolism
  • Fibroblasts / metabolism
  • Forensic Pathology
  • Immunohistochemistry
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Male
  • Mice
  • Neutrophils / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • Nitric Oxide Synthase Type III / metabolism
  • Skin / injuries*
  • Skin / metabolism*
  • Time Factors
  • Wound Healing*
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Nitric Oxide Synthase Type II
  • Nitric Oxide Synthase Type III
  • Nos2 protein, mouse
  • Nos3 protein, mouse
  • JNK Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Calpain
  • Caspases