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Item Type: | Article |
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Title: | Lymphoid to myeloid cell trans-differentiation is determined by C/EBPβ structure and post-translational modifications |
Creators Name: | Stoilova, B., Kowenz-Leutz, E., Scheller, M. and Leutz, A. |
Abstract: | The transcription factor C/EBP{beta} controls differentiation, proliferation, and functionality of many cell types, including innate immune cells. A detailed molecular understanding of how C/EBP{beta} directs alternative cell fates remains largely elusive. A multitude of signal-dependent post-translational modifications (PTMs) differentially affect the protean C/EBP{beta} functions. In this study we apply an assay that converts primary mouse B lymphoid progenitors into myeloid cells in order to answer the question how C/EBP{beta} regulates (trans-) differentiation and determines myeloid cell fate. We found that structural alterations and various C/EBP{beta} PTMs determine the outcome of trans-differentiation of lymphoid into myeloid cells, including different types of monocytes/macrophages, dendritic cells, and granulocytes. The ability of C/EBP{beta} to recruit chromatin remodeling complexes is required for the granulocytic trans-differentiation outcome. These novel findings reveal that PTMs and structural plasticity of C/EBP{beta} are adaptable modular properties that integrate and rewire epigenetic functions to direct differentiation to diverse innate immune system cells, which are crucial for the organism survival. |
Keywords: | Amino Acid Substitution, B-Lymphocytes, CCAAT-Enhancer-Binding Protein-beta, Cell Transdifferentiation, Cultured Cells, Innate Immunity, Myeloid Cells, Post-Translational Protein Processing, Tertiary Protein Structure, Transcriptional Activation, Transcriptome, Animals, Mice |
Source: | PLoS ONE |
ISSN: | 1932-6203 |
Publisher: | Public Library of Science |
Volume: | 8 |
Number: | 6 |
Page Range: | e65169 |
Date: | 5 June 2013 |
Official Publication: | https://doi.org/10.1371/journal.pone.0065169 |
PubMed: | View item in PubMed |
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