Establishment of a novel granulocytic sarcoma cell line which can adhere to dermal fibroblasts from a patient with granulocytic sarcoma in dermal tissues and myelofibrosis

Br J Haematol. 1992 Sep;82(1):26-31. doi: 10.1111/j.1365-2141.1992.tb04589.x.

Abstract

A novel human myeloid cell line, designated HSM-1, has been established from the pleural effusion of a patient with granulocytic sarcoma (GS) who had been followed as having primary myelofibrosis for 10 years. When he was diagnosed as having granulocytic sarcoma in dermal tissues, no evidence of malignant transformation into leukaemia was found in both the peripheral blood and bone marrow. The established cell line was positive for myeloperoxidase, Sudan black B, Naphthol AS-D chloroacetate esterase. Surface marker analysis revealed that HSM-1 expressed CD4, CD13, CD11a, CD11b, Leu8, CD49b, CD49d, CD49e, CD29 and HLA-DR. To clarify why the unusual myeloid tumours developed in non-haematopoietic tissues, we examined the capability of HSM-1 to bind to skin fibroblast layers. The HSM-1 cells were found to bind to both bone marrow stromal layers and skin fibroblast layers. Among the other myeloid cell lines tested, none was found to bind to skin fibroblast layers. These findings suggest that the GS cell line may be derived from a haematopoietic precursor cell which can bind to skin fibroblasts and is localized in non-haematopoietic tissues resulting in the formation of extramedullary myeloid metaplasia. HSM-1 is a useful tool for analysing the characteristics of granulocytic sarcoma and homing receptors for haematopoietic stem cells.

Publication types

  • Case Reports

MeSH terms

  • Antigens, Surface / analysis
  • Bone Marrow / pathology
  • Cell Adhesion / physiology
  • Cell Adhesion Molecules / analysis
  • Cell Line
  • Fibroblasts / metabolism
  • Humans
  • Leukemia, Myeloid / etiology
  • Leukemia, Myeloid / pathology*
  • Male
  • Middle Aged
  • Primary Myelofibrosis / complications*
  • Skin / pathology*
  • Skin Neoplasms / etiology
  • Skin Neoplasms / pathology*
  • Tumor Cells, Cultured / pathology

Substances

  • Antigens, Surface
  • Cell Adhesion Molecules