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関連する概念動画

Maintenance of the ES Cell State01:14

Maintenance of the ES Cell State

The cells of the blastocyst inner cell mass only remain pluripotent for a short time. This state of pluripotency and self-renewal can be maintained in embryonic stem (ES) cell culture by adding specific chemicals or growth factors to ensure the cells can continue dividing and later differentiate into different cell types. In some cases, the cells are grown on a feeder layer of differentiated cells, which provides the growth factors and extracellular matrix components necessary for stem cell...
EPS and iPS Cells in Disease Research01:21

EPS and iPS Cells in Disease Research

Embryonic and induced pluripotent stem cells are excellent models for disease research because of their ability to self-renew and differentiate into most cell types. Somatic cells from a patient are isolated and reprogrammed into induced pluripotent stem cells or iPSCs. These iPSCs are later differentiated into the desired cell type, which mirrors the diseased cell of the patient. In this way, disease models have been created for investigating diseases such as Down syndrome, type I diabetes,...
Induced Pluripotent Stem Cells01:13

Induced Pluripotent Stem Cells

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 called induced pluripotent stem...

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関連する実験動画

Updated: Jun 25, 2026

Generation of Induced Pluripotent Stem Cells by Reprogramming Mouse Embryonic Fibroblasts with a Four Transcription Factor, Doxycycline Inducible Lentiviral Transduction System
11:48

Generation of Induced Pluripotent Stem Cells by Reprogramming Mouse Embryonic Fibroblasts with a Four Transcription Factor, Doxycycline Inducible Lentiviral Transduction System

Published on: November 13, 2009

ESCの多能性にはRESTが必要ですか?

Helle F Jørgensen1, Zhou-Feng Chen, Matthias Merkenschlager

  • 1Lymphocyte Development Group, MRC Clinical Sciences Centre, Imperial College School of Medicine, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK. helle.jorgensen@imperial.ac.uk

Nature
|February 27, 2009
PubMed
まとめ

DNA結合タンパク質のRESTは,胚性幹細胞 (ESC) の多能性を維持するために不可欠ではありません. REST機能の喪失は,経済社会委員会が自己更新と差別化の可能性を保持することを妨げるものではない.

科学分野:

  • 分子生物学は分子生物学である.
  • 幹細胞生物学 幹細胞生物学
  • 遺伝学 遺伝学とは

背景:

  • DNA結合タンパク質REST (RE1静止転写因子),NRSF (ニューロン制限性静止因子) とも呼ばれ,転写抑制剤である.
  • RESTは,ヒトとマウスの胚性幹細胞 (ESC) で豊富に存在し,多数のニューロン遺伝子を標的としています.
  • 最近の研究では,RESTがESCの自己再生と多能性を制御することを示唆しており,RESTが障害したESCにおけるアルカリリンフォスファタゼの活性低下と多能性遺伝子の発現を理由としている.

さらに関連する動画

Reprogramming Induced Pluripotent Stem Cell Lines from Frozen Buffy Coat Samples
09:29

Reprogramming Induced Pluripotent Stem Cell Lines from Frozen Buffy Coat Samples

Published on: April 10, 2026

Generating iPS Cells from MEFS through Forced Expression of Sox-2, Oct-4, c-Myc, and Klf4
13:02

Generating iPS Cells from MEFS through Forced Expression of Sox-2, Oct-4, c-Myc, and Klf4

Published on: April 7, 2008

関連する実験動画

Last Updated: Jun 25, 2026

Generation of Induced Pluripotent Stem Cells by Reprogramming Mouse Embryonic Fibroblasts with a Four Transcription Factor, Doxycycline Inducible Lentiviral Transduction System
11:48

Generation of Induced Pluripotent Stem Cells by Reprogramming Mouse Embryonic Fibroblasts with a Four Transcription Factor, Doxycycline Inducible Lentiviral Transduction System

Published on: November 13, 2009

Reprogramming Induced Pluripotent Stem Cell Lines from Frozen Buffy Coat Samples
09:29

Reprogramming Induced Pluripotent Stem Cell Lines from Frozen Buffy Coat Samples

Published on: April 10, 2026

Generating iPS Cells from MEFS through Forced Expression of Sox-2, Oct-4, c-Myc, and Klf4
13:02

Generating iPS Cells from MEFS through Forced Expression of Sox-2, Oct-4, c-Myc, and Klf4

Published on: April 7, 2008