Dissecting Interferon-Induced Transcriptional Programs in Human Peripheral Blood CellsReport as inadecuate

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Interferons are key modulators of the immune system, and are central to the control of many diseases. The response of immune cells to stimuli in complex populations is the product of direct and indirect effects, and of homotypic and heterotypic cell interactions. Dissecting the global transcriptional profiles of immune cell populations may provide insights into this regulatory interplay. The host transcriptional response may also be useful in discriminating between disease states, and in understanding pathophysiology. The transcriptional programs of cell populations in health therefore provide a paradigm for deconvoluting disease-associated gene expression profiles.We used human cDNA microarrays to 1 compare the gene expression programs in human peripheral blood mononuclear cells PBMCs elicited by 6 major mediators of the immune response: interferons α, β, ω and γ, IL12 and TNFα; and 2 characterize the transcriptional responses of purified immune cell populations CD4+ and CD8+ T cells, B cells, NK cells and monocytes to IFNγ stimulation. We defined a highly stereotyped response to type I interferons, while responses to IFNγ and IL12 were largely restricted to a subset of type I interferon-inducible genes. TNFα stimulation resulted in a distinct pattern of gene expression. Cell type-specific transcriptional programs were identified, highlighting the pronounced response of monocytes to IFNγ, and emergent properties associated with IFN-mediated activation of mixed cell populations. This information provides a detailed view of cellular activation by immune mediators, and contributes an interpretive framework for the definition of host immune responses in a variety of disease settings.

Author: Simon J. Waddell , Stephen J. Popper, Kathleen H. Rubins, Michael J. Griffiths, Patrick O. Brown, Michael Levin, David A. Relman

Source: http://plos.srce.hr/


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