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相关概念视频

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

Methods of Nuclear Reprogramming

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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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T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

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T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
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相关实验视频

Updated: Jul 2, 2025

Selecting and Isolating Colonies of Human Induced Pluripotent Stem Cells Reprogrammed from Adult Fibroblasts
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Selecting and Isolating Colonies of Human Induced Pluripotent Stem Cells Reprogrammed from Adult Fibroblasts

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通过SEED-Selection在多个位置进行超高效率的T细胞重编程.

Christopher R Chang1,2,3,4, Vivasvan S Vykunta1,2,3,4, Daniel B Goodman1,2,5

  • 1Gladstone-UCSF Institute of Genomic Immunology, San Francisco, CA, USA.

bioRxiv : the preprint server for biology
|February 19, 2024
PubMed
概括

一种新的一步方法,即合成外因子/表达干扰剂 (SEEDs),可以有效地丰富基因编辑的T细胞. 这个过程通过去除不需要的细胞来提高复杂的细胞疗法的纯度.

科学领域:

  • 细胞免疫疗法细胞免疫疗法
  • 基因编辑技术 基因编辑技术
  • 生物制造过程中的生物制造工艺.

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Stem Cell-Derived Viral Ag-Specific T Lymphocytes Suppress HBV Replication in Mice
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Selecting and Isolating Colonies of Human Induced Pluripotent Stem Cells Reprogrammed from Adult Fibroblasts
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背景情况:

  • 目前的T细胞疗法由于工程不完整,往往导致异质细胞混合物.
  • 制造业的挑战限制了复杂多重基因编辑T细胞疗法的临床应用.

结论:

  • 种子提供了一种简单而可适应的方法,用于生产高度纯净,复杂的基因编辑T细胞.
  • 这项技术有助于开发下一代细胞疗法.
  • 促进复杂的基因编辑细胞疗法的生产.