This report describes a salvage pathway whereby activated T lymphocytes revert to nonproliferating cells in the absence of antigen or mitogenic signals. After the removal of mitogenic cytokines, cultured T lymphocytes cease dividing and rapidly begin to undergo cell death. However, the addition of fibroblasts to interleukin 2 (IL-2)-propagated T cells results in prolonged survival of the previously activated T lymphocytes in the absence of proliferation. The prevention of cell death is also achieved by conditioned medium from the fibroblasts. T lymphocytes cultured with fibroblasts or the conditioned medium retain the ability to be restimulated if mitogenic stimuli are added to the culture. The activity is not accounted for by IL-1-7. The studies suggest a stromal cell-mediated, nonspecific mechanism for survival of primed T lymphocytes in a nonproliferating state.
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1 December 1990
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December 01 1990
Fibroblasts mediate T cell survival: a proposed mechanism for retention of primed T cells.
S Scott,
S Scott
Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston 02114.
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F Pandolfi,
F Pandolfi
Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston 02114.
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J T Kurnick
J T Kurnick
Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston 02114.
Search for other works by this author on:
S Scott
Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston 02114.
F Pandolfi
Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston 02114.
J T Kurnick
Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston 02114.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1990) 172 (6): 1873–1876.
Citation
S Scott, F Pandolfi, J T Kurnick; Fibroblasts mediate T cell survival: a proposed mechanism for retention of primed T cells.. J Exp Med 1 December 1990; 172 (6): 1873–1876. doi: https://doi.org/10.1084/jem.172.6.1873
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