Abstract
Bcl-6 and Blimp-1 have recently been identified as key transcriptional regulators of effector and memory differentiation in CD4(+) T cells and CD8(+) T cells. Bcl-6 and Blimp-1 were previously known to be critical regulators of effector and memory differentiation of B lymphocytes. The new findings unexpectedly point to the Bcl-6 and Blimp-1 regulatory axis as a ubiquitous mechanism for controlling effector and memory lymphocyte differentiation and function. Bcl-6 and Blimp-1 are antagonistic transcription factors and can function as a self-reinforcing genetic switch for cell-fate decisions. However, their influences in different lymphocytes are complex. Here we review and examine the commonalities and differences in the functions of these transcription factors in CD4(+) follicular helper T(FH) lymphocytes, effector CD8(+) T lymphocytes and B lymphocytes.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Animals
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B-Lymphocytes / cytology*
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B-Lymphocytes / immunology
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B-Lymphocytes / metabolism
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Cell Differentiation / genetics
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Cell Differentiation / immunology*
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DNA-Binding Proteins / genetics
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DNA-Binding Proteins / immunology*
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DNA-Binding Proteins / metabolism
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Humans
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Immunologic Memory / genetics
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Immunologic Memory / immunology
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Lymphocyte Activation / genetics
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Lymphocyte Activation / immunology
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Positive Regulatory Domain I-Binding Factor 1
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Proto-Oncogene Proteins c-bcl-6
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Repressor Proteins / genetics
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Repressor Proteins / immunology*
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Repressor Proteins / metabolism
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T-Lymphocytes / cytology*
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T-Lymphocytes / immunology
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T-Lymphocytes / metabolism
Substances
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BCL6 protein, human
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DNA-Binding Proteins
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Proto-Oncogene Proteins c-bcl-6
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Repressor Proteins
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PRDM1 protein, human
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Positive Regulatory Domain I-Binding Factor 1