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Videos de Conceptos Relacionados

NF-κB-dependent Signaling Pathway02:26

NF-κB-dependent Signaling Pathway

The transcription factor NF-κB was discovered in 1986 in the lab of Nobel laureate Professor David Baltimore, for its interaction with the immunoglobulin light chain enhancer in B-cells. After more than three decades of study, it is now evident that NF-κB regulates the expression of over 100 genes. Most of these genes play an essential role in the innate and adaptive immune responses as well as the inflammatory responses of animals.
NF-κB-dependent Signaling Mechanism
The heterodimer of NF-κB...
TGF - β Signaling Pathway01:16

TGF - β Signaling Pathway

The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors are of three kinds RI, RII, and RIII. The RI...
The Two-State Receptor Model01:29

The Two-State Receptor Model

The two-state receptor model explains a drug's interaction with receptors, such as G protein-coupled receptors and ligand-gated ion channels, to induce or inhibit a biological response. When no natural ligands are present, a receptor exists in an equilibrium of inactive (Ri) and active (Ra) conformations. The inactive form does not produce a response, while the active form generates a basal effect known as constitutive activity.
The binding affinity of a drug determines its interaction with one...
Diversity of Antigen Receptors01:28

Diversity of Antigen Receptors

Antigen receptors are essential components of the immune system crucial in defending the body against foreign invaders. These receptors are present on the surface of B and T cells, enabling them to recognize antigens and mount an appropriate immune response.
Before encountering any antigen, lymphocytes express these receptors. On B cells, the antigen receptor is a membrane-bound antibody molecule called BCR; on T cells, it is a T cell receptor or TCR. B and T cell receptors are composed of two...
T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

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...
T Cell Types and Functions01:24

T Cell Types and Functions

When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...

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Video Experimental Relacionado

Updated: May 11, 2026

A TIRF Microscopy Technique for Real-time, Simultaneous Imaging of the TCR and its Associated Signaling Proteins
16:10

A TIRF Microscopy Technique for Real-time, Simultaneous Imaging of the TCR and its Associated Signaling Proteins

Published on: March 22, 2012

El receptor TNF 1: un complejo de personalidad dividido.

Bryan C Barnhart1, Marcus E Peter

  • 1The Ben May Institute for Cancer Research, University of Chicago, 924 East 57th Street, Chicago, IL 60637, USA.

Cell
|July 31, 2003
PubMed
Resumen
Este resumen es generado por máquina.

La señalización del receptor del factor de necrosis tumoral 1 (TNFR1) implica dos complejos que controlan la apoptosis. El primer complejo puede activar señales de supervivencia, actuando como un punto de control para regular la muerte celular.

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Last Updated: May 11, 2026

A TIRF Microscopy Technique for Real-time, Simultaneous Imaging of the TCR and its Associated Signaling Proteins
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Área de la Ciencia:

  • Biología celular Biología celular.
  • La señalización molecular.
  • Investigación de la investigación de la apoptosis.

Sus antecedentes:

  • El receptor del factor de necrosis tumoral 1 (TNFR1) es un miembro clave de la superfamilia de receptores de muerte.
  • Se sabe que las vías de señalización de TNFR1 regulan tanto la supervivencia celular como la muerte celular programada (apoptosis).

Objetivo del estudio:

  • Para dilucidar los mecanismos moleculares secuenciales que subyacen a la señalización apoptótica mediada por TNFR1.
  • Investigar el papel de distintas formaciones complejas de proteínas en el control de las decisiones del destino celular.

Principales métodos:

  • El estudio incluyó el análisis de la formación temporal de complejos proteicos aguas abajo de la activación de TNFR1.
  • Investigó la interacción funcional entre los complejos de señalización temprana y tardía.

Principales resultados:

  • La señalización apoptótica de TNFR1 ocurre a través del ensamblaje secuencial de dos complejos moleculares distintos.
  • La formación compleja inicial es capaz de activar las vías pro-supervivencia.
  • La actividad del segundo complejo es modulada por el primer complejo, estableciendo un punto de control regulatorio.

Conclusiones:

  • La señalización TNFR1 integra las vías de supervivencia y muerte a través de un mecanismo de formación complejo secuencial.
  • Esta formación compleja secuencial actúa como un punto de control crítico, asegurando la ejecución regulada de la apoptosis.