Regulation of growth factors-associated cell migration by C-phycocyanin scaffold in dermal wound healing

Clin Exp Pharmacol Physiol. 2012 Jan;39(1):13-9. doi: 10.1111/j.1440-1681.2011.05627.x.

Abstract

1. The present study examined the role of C-phycocyanin (C-pc) in relation to growth factors and cell migration during wound healing. 2. Histological and biochemical studies showed that C-pc scaffold significantly (P < 0.01) increased hydroxyl proline, total hexamine and protein content, and decreased uronic acid content in the wound tissues during a time course study in newly formed skin. 3. Reverse transcription polymerase chain reaction array of mouse growth factors in wound tissue showed overexpression (up to 10-fold) of growth factors, such as Cxcl12, Fgf18, Lefty 1, Lefty 2, Rabep 1 and Zip91, and downregulation (up to -10-fold) of Amh, Bmp 7 and Nodal genes in a 6-day period in C-pc treated groups. Also, Csf 3, Fgf 22, Mdk, Igf 2, transforming growth factor (TGF)-α 1 and interleukin (IL)-1β showed an upregulation of more than 30-fold than the control groups. TGF-β subfamily cytokine growth factors, such as Bmp 2, 4 and 8b, and other growth factors, such as Cxcl 1, showed the highest activity on day 3, showing a transient type of regulation. Western blot analysis showed a positive correlation between gene activity and protein expressions of Bmp 8b, Bmp4, Bmp2 and Cxcl 1. Day 6 in the C-pc group showed the highest csf3 and IL-1β expression. 4. C-pc had no direct effect on keratinocyte migration. However, keratinocytes that were co-cultured with fibroblasts showed a significantly higher rate of migration in the presence of C-pc, showing an indirect effect of C-pc on keratinocyte migration. 5. In conclusion, biodegradable C-pc scaffold might help to serve as an alternate scaffold material for wound healing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Cell Line
  • Cell Movement / drug effects*
  • Coculture Techniques
  • Collagen / biosynthesis
  • Fibroblasts / cytology
  • Fibroblasts / drug effects
  • Gene Expression Profiling
  • Gene Expression Regulation / drug effects*
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Keratinocytes / chemistry
  • Keratinocytes / cytology
  • Keratinocytes / drug effects
  • Keratinocytes / metabolism
  • Male
  • Mice
  • Mice, Inbred ICR
  • Oligonucleotide Array Sequence Analysis
  • Phycocyanin / pharmacology*
  • Phycocyanin / ultrastructure
  • Skin / chemistry
  • Skin / drug effects*
  • Skin / injuries
  • Skin / pathology
  • Specific Pathogen-Free Organisms
  • Tensile Strength / drug effects
  • Tissue Scaffolds / chemistry*
  • Wound Healing / drug effects*

Substances

  • Biomarkers
  • Intercellular Signaling Peptides and Proteins
  • Phycocyanin
  • Collagen