Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1995 Jun;73(3):205-11.
doi: 10.1038/icb.1995.34.

SV40-adenovirus immortalized cell lines derived from mouse lymphoid dendritic cell preparations

Affiliations

SV40-adenovirus immortalized cell lines derived from mouse lymphoid dendritic cell preparations

K Ohnishi et al. Immunol Cell Biol. 1995 Jun.

Abstract

Dendritic cells (DC) are antigen-presenting cells characteristic in their rarity and potent ability to stimulate resting T cells. We established several cell lines from purified mouse spleen DC and Langerhans' cells (LC) by infecting them with recombinant SV40ori(-)-adenovirus. Using this method, cells from these fractions are efficiently transformed at a frequency as high as 5 x 10(-6). Some established lines have dendritic morphology, express surface markers specific for DC (defined by mAb 33D1 and NLDC145) and weak substrate adherence. Interestingly, these lines simultaneously express B cell markers (B220 and Ly-1) and/or macrophage markers (Mac-1 and F4/80). Among the lines, OT6.2 and OT8.3.1 have retained stimulating activity in mixed lymphocyte reactions (MLR) which is attributable to the primary T cell stimulating activity of native DC. However, these lines also present soluble antigens to T cell clones, a secondary T cell stimulating activity, characteristic of B cells and macrophages. Although transformation has perturbed the functional discreteness of the DC cell lineage, DC-specific properties are partially preserved in the cell lines. These cell lines may provide useful experimental systems for the elucidation of molecular mechanisms involved in the MLR and the differentiation of DC.

PubMed Disclaimer

Publication types

Substances

LinkOut - more resources