Host-derived pericytes and Sca-1+ cells predominate in the MART-1- stroma fraction of experimentally induced melanoma

J Histochem Cytochem. 2011 Dec;59(12):1060-75. doi: 10.1369/0022155411428078.

Abstract

Identification of cell types in tumor-associated stroma that are involved in the development of melanoma is hampered by their heterogeneity. The authors used flow cytometry and immunohistochemistry to demonstrate that anti-MART-1 antibodies can discriminate between melanoma and stroma cells. They investigated the cellular composition of the MART-1-, non-hematopoietic melanoma-associated stroma, finding it consisted mainly of Sca-1+ and CD146+ cells. These cell types were also observed in the skin and muscle adjacent to developing melanomas. The Sca-1+ cell population was observed distributed in the epidermis, hair follicle bulges, and tumor capsule. The CD146+ population was found distributed within the tumor, mainly associated with blood vessels in a perivascular location. In addition to a perivascular distribution, CD146+ cells expressed α-smooth muscle actin, lacked expression of endothelial markers CD31 and CD34, and were therefore identified as pericytes. Pericytes were found to be associated with CD31+ endothelial cells; however, some pericytes were also observed associated with CD31-, MART-1+ B16 melanoma cells that appeared to form blood vessel structures. Furthermore, the authors observed extensive nuclear expression of HIF-1α in melanoma and stroma cells, suggesting hypoxia is an important factor associated with the melanoma microenvironment and vascularization. The results suggest that pericytes and Sca-1+ stroma cells are important contributors to melanoma development.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Ly / metabolism*
  • CD146 Antigen / metabolism
  • Cell Hypoxia
  • Cell Line, Tumor
  • Endothelium, Vascular / metabolism
  • Endothelium, Vascular / pathology
  • Flow Cytometry
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Immunohistochemistry
  • MART-1 Antigen / metabolism*
  • Melanoma, Experimental / blood supply
  • Melanoma, Experimental / metabolism
  • Melanoma, Experimental / pathology*
  • Membrane Proteins / metabolism*
  • Mesenchymal Stem Cells / metabolism
  • Mice
  • Mice, Inbred ICR
  • Mice, SCID
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • Neoplasm Transplantation
  • Neovascularization, Pathologic / metabolism
  • Neovascularization, Pathologic / pathology
  • Pericytes / metabolism
  • Pericytes / pathology*
  • Skin / metabolism
  • Skin / pathology
  • Stromal Cells / metabolism
  • Time Factors
  • Tumor Microenvironment

Substances

  • Antigens, Ly
  • CD146 Antigen
  • Hif1a protein, mouse
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Ly6a protein, mouse
  • MART-1 Antigen
  • Mcam protein, mouse
  • Membrane Proteins