Reconstruction of monocyte transcriptional regulatory network accompanies monocytic functions in human fibroblasts

Transcriptional regulatory networks (TRN) control the underlying mechanisms behind cellular functions and they are defined by a set of core transcription factors regulating cascades of peripheral genes. Here we report SPI1, CEBPA, MNDA and IRF8 as core transcription factors of monocyte TRN and demon...

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Published inPloS one Vol. 7; no. 3; p. e33474
Main Authors Suzuki, Takahiro, Nakano-Ikegaya, Mika, Yabukami-Okuda, Haruka, de Hoon, Michiel, Severin, Jessica, Saga-Hatano, Satomi, Shin, Jay W, Kubosaki, Atsutaka, Simon, Christophe, Hasegawa, Yuki, Hayashizaki, Yoshihide, Suzuki, Harukazu
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 13.03.2012
Public Library of Science (PLoS)
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Summary:Transcriptional regulatory networks (TRN) control the underlying mechanisms behind cellular functions and they are defined by a set of core transcription factors regulating cascades of peripheral genes. Here we report SPI1, CEBPA, MNDA and IRF8 as core transcription factors of monocyte TRN and demonstrate functional inductions of phagocytosis, inflammatory response and chemotaxis activities in human dermal fibroblasts. The Gene Ontology and KEGG pathway analyses also revealed notable representation of genes involved in immune response and endocytosis in fibroblasts. Moreover, monocyte TRN-inducers triggered multiple monocyte-specific genes based on the transcription factor motif response analysis and suggest that complex cellular TRNs are uniquely amenable to elicit cell-specific functions in unrelated cell types.
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Conceived and designed the experiments: TS Y. Hasegawa Y. Hayashizaki HS. Performed the experiments: TS MNI HYO SSH AK CS. Analyzed the data: TS JS MDH. Wrote the paper: TS JWS HS.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0033474