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Related Concept Videos

Introduction to Nuclear Reprogramming01:14

Introduction to Nuclear Reprogramming

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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Somatic to iPS Cell Reprogramming

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 for this...
Methods of Nuclear Reprogramming01:24

Methods of Nuclear Reprogramming

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 injury repair.

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Related Experiment Video

Updated: May 13, 2026

Efficient Generation Human Induced Pluripotent Stem Cells from Human Somatic Cells with Sendai-virus
09:43

Efficient Generation Human Induced Pluripotent Stem Cells from Human Somatic Cells with Sendai-virus

Published on: April 24, 2014

Sendai virus persistence questions the transient naive reprogramming method for iPSC generation.

Alejandro De Los Angeles1, Clemens B Hug2, Vadim N Gladyshev3

  • 1McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge MA, USA.

Biorxiv : the Preprint Server for Biology
|April 1, 2024
PubMed
Summary

Transient naive treatment (TNT) may improve induced pluripotent stem cells (iPSCs), but persistent Sendai virus expression can alter reprogramming factors. Further research is needed for transgene-independent iPSC generation.

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Published on: July 11, 2019

Area of Science:

  • Stem cell biology
  • Epigenetics
  • Developmental biology

Background:

  • Induced pluripotent stem cells (iPSCs) offer an alternative to embryonic stem cells (ESCs) but exhibit epigenetic and developmental differences.
  • A recent study proposed transient naive treatment (TNT) to enhance human iPSC (hiPSC) reprogramming and developmental potential.

Approach:

  • The study re-evaluated the TNT method by analyzing bulk hiPSCs and investigating persistent Sendai virus expression.
  • Assessed the impact of continuous naive media on Sendai gene expression and reprogramming factors (MYC, SOX2, KLF4).

Key Points:

  • Sendai virus genes were detected in control pluripotent stem cell (PSC) samples, including human ESCs (hESCs).
  • Continuous naive media treatment led to elevated Sendai expression and overexpression of exogenous MYC, SOX2, and KLF4.
  • This altered the expression levels and ratios of key reprogramming factors in hiPSCs.

Conclusions:

  • The effectiveness of the TNT method requires re-evaluation considering potential confounding factors like persistent viral gene expression.
  • Future research should focus on delivery methods ensuring rapid elimination of exogenous factors for generating true transgene-independent iPSCs.
  • Ensuring prompt clearance of viral vectors is crucial for accurate assessment of reprogramming strategies and generating bona fide iPSCs.