{"id":3734,"date":"2019-06-08T14:22:09","date_gmt":"2019-06-08T05:22:09","guid":{"rendered":"http:\/\/163.180.4.222\/lab\/?p=3734"},"modified":"2019-06-08T14:22:09","modified_gmt":"2019-06-08T05:22:09","slug":"cell-fate-decisions-during-development","status":"publish","type":"post","link":"https:\/\/biochemistry.khu.ac.kr\/lab\/?p=3734","title":{"rendered":"Cell fate decisions during development"},"content":{"rendered":"

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The shape of our nose, the color of our skin, the movement of our gut, all depend on an extraordinary cell type called neural crest cells, which originate during embryogenesis. Since their discovery in 1868 (1<\/em><\/a>), neural crest cells, which are present in all vertebrates, have fascinated developmental biologists (2<\/em><\/a>). One of the amazing features of neural crest cells is their extraordinary multipotency: They form cartilage, muscle, neurons, glia, pigment cells, adrenal cells, and so on. (3<\/em><\/a>). No other embryonic cell type can differentiate into so many different kinds of cells. However, how this multipotency is achieved is not understood. On page 971 of this issue, Soldatov\u00a0et al.<\/em>\u00a0(4<\/em><\/a>) clarify some of the mechanisms that explain how the multiplicity of cell types is generated by neural crest cells.<\/p>\n

The neural crest is an embryonic stem cell population that is initially formed in an embryonic tissue layer called the ectoderm. The ectoderm will also form the neural tube, which later becomes the central nervous system. The neural crest is formed adjacent to the neural tube, in a region called the neural plate border, from where cells delaminate, migrate to colonize different tissues, and then differentiate (3<\/em><\/a>,\u00a05<\/em><\/a>). It has been shown using genetic labeling that neural crest cells are multipotent when they leave the neural tube and that their fate is decided after delamination (6<\/em><\/a>\u20138<\/em><\/a>), but how this multipotency is controlled has remained elusive.<\/p>\n

Once neural crest cells are formed in the ectoderm, one of the first steps in their development is to delaminate and undergo an epithelial-to-mesenchymal transition (EMT), which is required for their migration (9<\/em><\/a>). The classical view of neural crest EMT is that this is an abrupt process that results from the activation of a gene regulatory network (10<\/em><\/a>). Soldatov\u00a0et al.<\/em>\u00a0show that this is not the case, as they are able to resolve a sequence of stages around delamination, demonstrating that pre-EMT neural crest cells express genes associated with neural plate border and neural tube identity. More advanced neural crest cells down-regulate the expression of neural tube markers and increase the expression of neural crest cell\u2013specific genes. This indicates that the transition from premigratory to migratory neural crest cells is more gradual and complex than initially thought.<\/p>\n

This view is consistent with recent reports showing that EMT in cancer cells is not an all-or-nothing process, but rather a complex event with many steps controlled by different genes: Different cells undergoing EMT activate different aspects of the gene expression program at different times (11<\/em><\/a>). Although the idea that EMT in the neural crest is not an abrupt process has been previously suggested (12<\/em><\/a>), Soldatov\u00a0et al.<\/em>\u00a0provide molecular evidence from single-cell RNA-sequencing data combined with spatial transcriptomics and lineage tracing in mouse neural crest differentiation. This allowed the identification of substages of EMT during delamination, characterized by specific marker expression.<\/p>\n

One of the most intriguing conclusions from Soldatov\u00a0et al.<\/em>\u00a0is the identification of specific steps involved in neural crest differentiation, in which progenitor cells undergo binary choices between possible fates as a result of their cellular history. This history is defined by the internal and external events that the cell has experienced, such as the autonomous activation of genes as well as signals from neighboring cells. Progenitor cells initially coactivate gene expression programs that lead to competing cellular fates (see the figure). These mutually exclusive cell fate programs then compete with each other. This competition is determined by differences in gene expression caused by historical changes that affect the transcriptome. Cells then up-regulate one program and down-regulate the other after a decision point (bifurcation). Thus, by inducing competing gene expression programs, the cell fate commitment process starts to look like a sequence of biasing factors that pull the cells in different directions, depending on their own history. It is likely that an interplay between these intrinsically developing biases interacts with extrinsic cues to shift the bias into a particular cell fate. This model challenges the current view in which neural crest cells abruptly activate only one of many alternative cell fate programs, leading to cell differentiation.<\/p>\n

This revised vision for neural crest cell differentiation is consistent with what has been proposed for the differentiation of other cell types, such as those of the hematopoietic lineage (13<\/em><\/a>). The first stable bifurcation identified in neural crest differentiation separates progenitors of the sensory lineage from those of autonomic and mesenchymal fates. This is followed by additional binary decisions that separate autonomic neuronal fate from mesenchymal differentiation. This contrasts with the current view in which a single precursor differentiates directly into specific cell types. In addition, Soldatov\u00a0et al.<\/em>show that many transcription factors considered as \u201cmaster regulators\u201d for specific lineages are not expressed at the time of the bifurcation to differentiate into these three lineages. This suggests that the activation of specific gene expression programs around the bifurcation point is triggered not by these master regulators, but by environmental conditions, such as chemical or mechanical cues (3<\/em><\/a>,\u00a014<\/em><\/a>).<\/p>\n

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