Leukemia Research
Volume 28, Issue 8 , Pages 869-877, August 2004

Induction of CD28 on the new myeloma cell line MOLP-8 with t(11;14)(q13;q32) expressing δ/λ type immunoglobulin

  • Yoshinobu Matsuo

      Affiliations

    • Fujisaki Cell Center, Hayashibara Biochemical Labs., Inc., 675-1 Fujisaki, Okayama 702-8006, Japan
    • Corresponding Author InformationCorresponding author. Tel.: +81-86-276-8621; fax: +81-86-274-2150.
  • ,
  • Hans G Drexler

      Affiliations

    • DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany
  • ,
  • Akira Harashima

      Affiliations

    • Fujisaki Cell Center, Hayashibara Biochemical Labs., Inc., 675-1 Fujisaki, Okayama 702-8006, Japan
  • ,
  • Ayumi Okochi

      Affiliations

    • Fujisaki Cell Center, Hayashibara Biochemical Labs., Inc., 675-1 Fujisaki, Okayama 702-8006, Japan
  • ,
  • Atsuhiko Hasegawa

      Affiliations

    • Department of 1st Internal Medicine, Ehime University School of Medicine, Shigenobu, Ehime, Japan
  • ,
  • Kensuke Kojima

      Affiliations

    • Department of 1st Internal Medicine, Ehime University School of Medicine, Shigenobu, Ehime, Japan
  • ,
  • Kunzo Orita

      Affiliations

    • Fujisaki Cell Center, Hayashibara Biochemical Labs., Inc., 675-1 Fujisaki, Okayama 702-8006, Japan

Received 31 October 2003; accepted 12 December 2003.

Abstract 

The novel multiple myeloma (MM) cell line MOLP-8 carrying the t(11;14) (q13;q32) was established from the peripheral blood of a 52-year-old Japanese male patient with Bence–Jones δ/λ type MM (stage IIIA with hyperammonemia). The growth of MOLP-8 cells is constitutively independent of exogenous growth factors or feeder cells. MOLP-8 cells grow mainly as free floating single cells and slightly adherent on the bottom of the plastic culture flask. Wright–Giemsa-stained MOLP-8 cells show the typical plasma cell morphology with abundant cytoplasm, heterogeneous cell size and one to three nuclei. The immunoprofile of MOLP-8 corresponds to that seen typically in primary MM cells: positive for cytoplasmic immunoglobulin (Ig) δ/λ chains, CD10, CD29, CD38, CD40, CD44, CD49b, CD49d, CD54, CD56, CD58, CD71, CD138 and PCA-1; the cells were negative for surface Igs and various other B-cell, T-cell and myelomonocyte-associated immunomarkers. CD28 became positive after co-culture of MOLP-8 cells with bone marrow adherent stromal (BST) feeder cells for a week. About 30% of MOLP-8 cells adhered strongly to the BST cells, but the cellular adhesion was clearly inhibited by addition of either anti-CD29 or anti-CD106 monoclonal antibody, suggesting a specific cellular adhesion through α4β1-integrin–VCAM-1 interaction. The novel MOLP-8 cell line together with the present myeloma cell lines will present useful model systems in the investigation of the biology of MM.

Keywords:  CD28, Cell adhesion, Cell line, Multiple myeloma

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PII: S0145-2126(03)00422-3

doi:10.1016/j.leukres.2003.12.008

Leukemia Research
Volume 28, Issue 8 , Pages 869-877, August 2004