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Derivation of Thymic Lymphoma T-cell Lines from Atm-/- and p53-/- Mice
Published on: April 3, 2011
Establishment and characterization of a mantle cell lymphoma cell line
1Department of Pathology, Chosun University Medical School, Kwangju, Korea.
Insights
A new mantle cell lymphoma (MCL) cell line, JeKo-1, was developed from patient cells. This cell line exhibits key MCL markers and is highly tumorigenic in mice, offering a valuable research model.
Area of Science:
- Hematology
- Oncology
- Cell Biology
Background:
- Mantle cell lymphoma (MCL) is an aggressive non-Hodgkin B-cell lymphoma.
- Establishing reliable cell lines is crucial for understanding MCL pathogenesis and developing therapies.
- The leukaemic large cell variant of MCL presents unique clinical and biological characteristics.
Observation:
- A novel MCL cell line, designated JeKo-1, was derived from the peripheral blood of a patient with leukaemic large cell MCL.
- JeKo-1 cells demonstrated a B-cell phenotype (IgM+, IgD+, CD5+, CD19+, CD20+) and were Epstein-Barr virus negative.
- These cells exhibited overexpression of key regulatory proteins including cyclin D1, Bcl-2, c-Myc, and Rb.
Findings:
- Polymerase chain reaction confirmed the characteristic Bcl-1/J(H) gene rearrangement, a hallmark of MCL.
- Karyotypic analysis revealed chromosomal abnormalities but lacked the typical t(11;14) translocation.
- JeKo-1 cells proved to be highly tumorigenic when xenografted into SCID mice.
Implications:
- The JeKo-1 cell line serves as a valuable in vitro and in vivo model for studying MCL, particularly the leukaemic large cell variant.
- This model can facilitate research into the molecular mechanisms driving MCL progression and drug resistance.
- Further characterization may reveal unique therapeutic vulnerabilities associated with this specific MCL subtype.
Abstract:
A mantle cell lymphoma (MCL) cell line (JeKo-1) was established from peripheral blood mononuclear cells of a patient with a large cell variant of MCL showing leukaemic conversion. JeKo-1 cells were Epstein-Barr virus negative and showed a B-cell phenotype with IgM+, IgD+, CD3-, CD5+, CD10-, CD19+, CD20+ and CD23-; they overexpressed cyclin D1, Bcl-2, c-Myc and Rb proteins. Bcl-1/J(H) gene rearrangement was confirmed by polymerase chain reaction, although karyotypic analysis showed 40/41 chromosomes devoid of apparent t(11;14)(q13;q32) translocation. JeKo-1 cells were highly tumourigenic in SCID mice.

