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Published on: April 8, 2016
An immortalized cell line with features of human follicular dendritic cells. Antigen and cytokine expression analysis
K Orscheschek1, H Merz, B Schlegelberger
1Institute of Pathology, Medical University of Lübeck, FRG.
Insights
Researchers developed a new immortalized cell line, FDC-H1, to study follicular dendritic cells (FDC). This cell line accurately mimics FDC surface antigens and cytokine profiles, aiding research into FDC biology and interactions.
Area of Science:
- Immunology
- Cell Biology
Background:
- Follicular dendritic cells (FDC) are crucial for immune responses within lymphoid follicles, presenting antigens to B cells.
- Isolating FDC for in vitro studies is challenging due to their low abundance and tendency to entrap lymphocytes.
- The monoclonal antibody Ki-M4 is a specific marker for identifying FDC.
Purpose of the Study:
- To establish a novel immortalized cell line that retains the characteristic features of human FDC.
- To facilitate in vitro research on FDC biology and their interactions with other cells.
Main Methods:
- Enrichment of FDC from human tonsils using a modified isolation procedure.
- Fusion of enriched FDC with the SP2/0-Ag14 myeloma cell line to create the hybridoma FDC-H1.
- Characterization of FDC-H1 using monoclonal antibody Ki-M4, surface antigen analysis, and semiquantitative reverse-transcribed polymerase chain reaction (RT-PCR) for cytokine mRNA profiles.
Main Results:
- The FDC-H1 cell line exhibits unlimited growth potential and consistently expresses the Ki-M4 antigen and other human FDC surface markers.
- FDC-H1 displays a cytokine/mRNA profile similar to primary FDC, with detectable levels of interleukin (IL)-1 alpha and surface CD23, and lacking mRNA for many common cytokines.
- A weak but constant IL-6 mRNA expression was detected in FDC-H1, with limited IL-6 transcripts observed in situ in tonsil dendritic cells.
Conclusions:
- FDC-H1 is the first established cell line that consistently expresses FDC-specific surface antigens and a characteristic cytokine profile.
- This novel cell line provides a valuable tool for studying FDC biology and their functional relationships with normal and neoplastic lymphoid cells.
Abstract:
Follicular dendritic cells (FDC) are specialized cells residing primarily within lymphoid follicles. They bind immunocomplexes and play an important role in the presentation of antigen to follicular B cells. Isolation of FDC for in vitro studies, however, is difficult because they constitute only about 1% of the cells in lymphoid tissue and form tight clusters entrapping lymphocytes within their dendritic processes. The monoclonal antibody (mAb) Ki-M4, which is highly restricted in its binding to FDC, is used to identify these cells. In order to establish a new immortalized cell line with features of FDC, we applied a modified procedure to isolate and enrich FDC from human tonsils and fused them with the myeloma cell line SP2/0-Ag14. The new hybrid cell line, designated FDC-H1, is of both mouse lymphoid and human FDC origin. FDC-H1 was found to have unlimited growth potential and to consistently express the Ki-M4 antigen and other surface antigens of human FDC. Semiquantitative reverse-transcribed polymerase chain reaction (RT-PCR) of enriched FDC and FDC-H1 revealed the same highly restricted cytokine/mRNA profile for both, with detectable levels of interleukin (IL)-1 alpha and surface CD23 and a lack of mRNA for IL-1 beta, IL-2, IL-3, IL-4, IL-7, IL-9, IL-10, interferon-gamma, tumor necrosis factor-alpha, transforming growth factor-beta and granulocyte/macrophage-colony-stimulating factor. Additionally a weak but constant IL-6 mRNA expression was found in the cell line FDC-H1 by RT-PCR. In situ hybridization experiments in tonsils revealed IL-6 transcripts in cells with a staining pattern characteristic of a dendritic cell only in a few germinal centers. To our knowledge, FDC-H1 is the first cell line that constantly expresses surface antigens and a cytokine profile characteristic of FDC. It is, therefore, well suited for studying the biology of FDC and the functional relationship between FDC and normal or neoplastic lymphatic cells.
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