Histomorphometric analysis of the phenotypical differentiation of recruited macrophages following subcutaneous implantation of an allogenous acellular dermal matrix

Int J Oral Maxillofac Surg. 2011 Apr;40(4):401-7. doi: 10.1016/j.ijom.2010.10.025. Epub 2010 Nov 27.

Abstract

This study aimed to clarify the phenotypical differentiation of recruited macrophages following subdermal implantation of an allogenous, acellular dermal matrix (aADM). In 20 male Wistar rats, one leg was randomly chosen for subcutaneous implantation of an aADM, while the other side received an autogenous dermis graft for control purposes. After 7 and 14 postoperative days, 10 animals were killed. Biopsies were obtained from the healing area and subjected to immunohistochemical staining (targets: pan macrophage marker CD68, M1 macrophage marker CD197, M2 macrophage marker CD163), histomorphometric analysis and reverse transcriptase polymerase chain reaction (targets: iNOS, arginase). No differences were detected in the total number of recruited macrophages between the groups. Allogenous ADMs significantly stimulated proinflammatory M1 differentiation, while autogenous dermis induced the regeneration promoting M2 phenotype. Proinflammatory M1 differentiation of macrophages might provide a potential explanation for profibrotic tissue deposition at the aADM interface following subcutaneous implantation, which has been observed previously.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / analysis
  • Antigens, Differentiation, Myelomonocytic / analysis
  • Arginase / analysis
  • Cell Differentiation
  • Collagen / adverse effects
  • Foreign-Body Reaction / etiology*
  • Immunophenotyping / methods*
  • Implants, Experimental* / adverse effects
  • Macrophages / classification
  • Macrophages / immunology*
  • Male
  • Nitric Oxide Synthase Type II / analysis
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Receptors, CCR7 / analysis
  • Receptors, Cell Surface / analysis
  • Skin Transplantation
  • Skin, Artificial* / adverse effects
  • Subcutaneous Tissue / immunology

Substances

  • Alloderm
  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD163 antigen
  • CD68 antigen, human
  • Receptors, CCR7
  • Receptors, Cell Surface
  • Collagen
  • Nitric Oxide Synthase Type II
  • Arginase