Phenotypic and molecular analysis of six human cell lines derived from patients with plasma cell dyscrasia

Br J Haematol. 1999 Sep;106(3):669-81. doi: 10.1046/j.1365-2141.1999.01602.x.

Abstract

Cell lines RPMI 8226, JJN3, U266 B1, NCI-H929 (all EBV-) and ARH77 and HS-Sultan (both EBV+) have been extensively characterized in this study. EBV- lines expressed the phenotype (CD138-, CD19+, CD20+) whereas EBV+ were (CD138+, CD19-, CD20-). CD56 expression was restricted to EBV- cell lines, with the exception of U266 B1, whereas PCA-1 was strongly expressed on five of the six cell lines. Only EBV+ cell lines bound peanut-agglutinin (PNA). However, all cell lines bound the lectin Jacalin that binds the same receptor as PNA, irrespective of the receptors sialylation status. By RT-PCR and direct sequencing of their IgH V/D/J domains, ARH77 was demonstrated to use the germline sequence VH4-34/dm1/JH6b, whereas no arrangement was demonstrated for RPMI 8226, suggesting IgH gene deletion or mutation. HLA class I and II antigens were detected using HLA typing on all cell lines warranting their use as suitable targets for HLA-restricted cytotoxic T cells. By sensitive RT-PCR, mRNA for IL-6, IL-6R and TNFbeta was found expressed in all cell lines. IL-1 mRNA expression was predominantly associated with the EBV+ phenotype. Although mRNA for IL-3 and GM-CSF was never detected, transcripts for c-kit ligand and, more commonly, its receptor were. Likewise GM-CSF, M-CSF and erythropoietin mRNA transcripts were detected in the majority of cell lines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Blotting, Southern
  • Cells, Cultured
  • Cytokines / metabolism
  • Gene Rearrangement
  • HLA Antigens / metabolism
  • Humans
  • Immunoglobulin Heavy Chains / genetics
  • Immunophenotyping
  • Molecular Sequence Data
  • Multiple Myeloma / genetics
  • Paraproteinemias / genetics*
  • Phenotype
  • RNA / analysis
  • Receptors, Cytokine / metabolism

Substances

  • Cytokines
  • HLA Antigens
  • Immunoglobulin Heavy Chains
  • Receptors, Cytokine
  • RNA