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Related Concept Videos

Somatic to iPS Cell Reprogramming01:29

Somatic to iPS Cell Reprogramming

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Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012...
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Methods of Nuclear Reprogramming01:24

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Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for...
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Introduction to Nuclear Reprogramming01:14

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Nuclear reprogramming is the process of switching gene expression of one cell type to that of another cell type, usually from a differentiated cell state to an undifferentiated cell state. Differentiation occurs during processes such as development and morphogenesis, tissue regeneration, and malignancy. Cells can also be artificially induced to reprogram their gene expression by techniques such as nuclear transfer, induced pluripotency, and cell fusion. Such techniques have many applications in...
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Chromatin Modification in iPS Cells01:32

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Chromatin modification alters gene expression; therefore, scientists can add histone-modifying enzymes, histone variants, and chromatin remodeling complexes to somatic cells to aid reprogramming into pluripotent stem (iPS) cells.
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
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Forced Transdifferentiation01:28

Forced Transdifferentiation

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Transdifferentiation, also known as lineage reprogramming, was first discovered by Selman and Kafatos in 1974 in silkmoths. They observed that the moths’ cuticle-producing cells transformed into salt-producing cells. Many such cases of natural transdifferentiation occur in organisms. In humans, pancreatic alpha cells can become beta cells. In newts, the loss of the eye’s lens causes the pigmented epithelial cells to transdifferentiate into the lens cells.
Artificial...
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Induced Pluripotent Stem Cells01:13

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Stem cells are undifferentiated cells that divide and produce different types of cells. Ordinarily, cells that have differentiated into a specific cell type are post-mitotic—that is, they no longer divide. However, scientists have found a way to reprogram these mature cells so that they “de-differentiate” and return to an unspecialized, proliferative state. These cells are also pluripotent like embryonic stem cells—able to produce all cell types—and are therefore...
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Cellular Reprogramming Using Defined Factors and MicroRNAs.

Takanori Eguchi1, Takuo Kuboki2

  • 1Division of Molecular and Cell Biology, Department of Radiation Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, 3 Blackfan Circle, Center for Life Science 6, Boston, MA 02115, USA; Department of Dental Pharmacology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Okayama 700-8525, Japan; Advanced Research Center for Oral and Craniofacial Sciences, Okayama University Dental School/Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8525, Japan.

Stem Cells International
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PubMed
Summary

Cellular reprogramming, including induced pluripotent stem cells (iPS cells), utilizes specific factors to revert cells to a stem-cell-like state. MicroRNAs like miRNA-720 play a role in this process by targeting key pluripotency factors.

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Area of Science:

  • Stem cell biology and regenerative medicine
  • Molecular biology and genetics
  • Developmental biology

Background:

  • Cellular differentiation is a complex process involving multiple stages, from zygotes to specialized cell lineages.
  • Induced pluripotent stem cells (iPS cells) represent a significant advancement, enabling the reprogramming of somatic cells into a pluripotent state.
  • Mesenchymal stem cells (MSCs) and dental pulp stem cells (DPSCs) are multipotent stem cells with unique microRNA expression profiles.

Purpose of the Study:

  • To review the historical development and current concepts in cellular reprogramming.
  • To highlight the role of reprogramming factors and microRNAs in cell fate determination.
  • To discuss the implications of cellular reprogramming in life science and medicine.

Main Methods:

  • Review of scientific literature on cellular reprogramming techniques.
  • Analysis of reprogramming factors such as Nanog, Klf5, Oct3/4, Sox2, and Myc.
  • Investigation of direct reprogramming methods using transcription factors and microRNAs.

Main Results:

  • Defined reprogramming factors have enabled the generation of iPS cells, revolutionizing regenerative medicine.
  • Direct reprogramming methods have been developed for generating specific cell types like myocytes and neurons.
  • MicroRNA-720 has been identified to influence cellular reprogramming by targeting Nanog and inducing DNA methyltransferases.

Conclusions:

  • Cellular reprogramming is a rapidly evolving field with profound implications for disease modeling and therapeutic applications.
  • Understanding the molecular mechanisms, including the role of microRNAs, is crucial for advancing reprogramming technologies.
  • The development of iPS cells and direct reprogramming techniques offers new avenues for regenerative medicine and personalized therapies.