Fas ligand: Difference between revisions

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'''Fas ligand''' (also known as '''FasL''', '''CD95L''', or '''CD178''') is a type-1 transmembrane protein that belongs to the [[tumor necrosis factor (TNF) family]]. It binds with the [[Fas receptor]] (CD95) to induce apoptosis, a process of programmed cell death. Fas ligand plays a crucial role in the regulation of the immune system and the progression of cancer.
{{Short description|A protein involved in the regulation of the immune system}}
{{DISPLAYTITLE:Fas Ligand}}


== Structure ==
==Overview==
Fas ligand is a type-II transmembrane protein, which means it has an extracellular C-terminal domain and a cytoplasmic N-terminal domain. The extracellular domain of Fas ligand is what interacts with the Fas receptor. The cytoplasmic domain is not required for apoptosis induction.
[[Fas ligand]] (FasL) is a type-II transmembrane protein that belongs to the [[tumor necrosis factor]] (TNF) family. It plays a crucial role in the regulation of the [[immune system]] and the induction of [[apoptosis]], or programmed cell death. FasL is primarily expressed on the surface of activated [[T cells]] and [[natural killer cells]], and it interacts with its receptor, [[Fas receptor]] (FasR), to trigger apoptotic signaling pathways.


== Function ==
==Structure==
The primary function of Fas ligand is to bind to the Fas receptor and initiate a series of events that lead to apoptosis. This process is critical for the regulation of the immune system. It helps to maintain immune homeostasis and prevent autoimmune diseases by killing off excess or harmful cells.
Fas ligand is a homotrimeric protein, meaning it forms a complex of three identical subunits. Each subunit consists of an extracellular domain, a transmembrane domain, and a short cytoplasmic tail. The extracellular domain is responsible for binding to the Fas receptor, initiating the apoptotic cascade.


Fas ligand is also involved in immune privilege, a state in which certain body sites are able to tolerate the introduction of antigens without eliciting an inflammatory immune response. This is achieved by Fas ligand-mediated apoptosis of invading immune cells.
==Function==
The primary function of Fas ligand is to induce apoptosis in target cells. This is a critical mechanism for maintaining immune homeostasis and preventing autoimmune diseases. When FasL binds to FasR on the surface of a target cell, it triggers a series of intracellular events that lead to cell death. This process is essential for the elimination of infected or cancerous cells and for the termination of immune responses.


== Role in Disease ==
===Role in Immune System===
Alterations in the Fas ligand/Fas receptor system can lead to various diseases. For example, mutations in the Fas ligand or Fas receptor can cause autoimmune lymphoproliferative syndrome (ALPS), a rare disorder characterized by non-malignant lymphoproliferation, autoimmunity, and increased risk of lymphoma.
Fas ligand is involved in several key processes within the immune system:


In cancer, Fas ligand expression can be a double-edged sword. On one hand, cancer cells can use Fas ligand to kill attacking immune cells and evade the immune response. On the other hand, therapies that enhance Fas ligand expression can be used to kill cancer cells.
* '''Activation-Induced Cell Death (AICD):''' FasL is crucial for AICD, a process that helps regulate the immune response by eliminating excess [[lymphocytes]] after an immune response.
* '''Peripheral Tolerance:''' FasL contributes to peripheral tolerance by inducing apoptosis in self-reactive T cells, thus preventing [[autoimmunity]].
* '''Cytotoxic T Lymphocyte (CTL) Function:''' CTLs use FasL to kill target cells, such as virus-infected cells or tumor cells, by inducing apoptosis.


== See Also ==
==Pathology==
Dysregulation of Fas ligand or its receptor can lead to various diseases:
 
* '''Autoimmune Diseases:''' Insufficient FasL activity can result in the survival of self-reactive lymphocytes, contributing to autoimmune conditions such as [[systemic lupus erythematosus]] and [[rheumatoid arthritis]].
* '''Cancer:''' Some cancer cells evade immune surveillance by downregulating FasR or expressing FasL to induce apoptosis in attacking immune cells.
* '''Immunodeficiency:''' Mutations in the Fas or FasL genes can lead to immunodeficiency syndromes, characterized by lymphoproliferation and increased susceptibility to infections.
 
==Clinical Applications==
Understanding the Fas/FasL system has implications for therapeutic interventions:
 
* '''Cancer Therapy:''' Strategies to enhance FasL-mediated apoptosis in tumor cells are being explored as potential cancer treatments.
* '''Autoimmune Disease Treatment:''' Modulating FasL activity could help in treating autoimmune diseases by promoting the deletion of autoreactive lymphocytes.
 
==Images==
[[File:FasL_structure.png|thumb|right|Diagram of Fas ligand structure showing its trimeric form.]]
[[File:FasL_pathway.png|thumb|left|Illustration of the Fas/FasL apoptotic pathway.]]
 
==Related pages==
* [[Apoptosis]]
* [[Apoptosis]]
* [[Fas receptor]]
* [[Tumor necrosis factor]]
* [[Tumor necrosis factor (TNF) family]]
* [[Immune system]]
* [[Autoimmune lymphoproliferative syndrome (ALPS)]]
* [[T cell]]
* [[Immune privilege]]
* [[Natural killer cell]]
 
== References ==
<references />


[[Category:Immunology]]
[[Category:Proteins]]
[[Category:Proteins]]
[[Category:Immunology]]
[[Category:Cell biology]]
[[Category:Apoptosis]]
[[Category:Apoptosis]]
{{Protein-stub}}
{{Immunology-stub}}
= Fas ligand =
<gallery>
File:Fas_ligand.jpg|Fas ligand
File:Fas_signaling.jpg|Fas signaling
File:Signal_transduction_pathways.svg|Signal transduction pathways
</gallery>

Revision as of 17:33, 18 February 2025

A protein involved in the regulation of the immune system



Overview

Fas ligand (FasL) is a type-II transmembrane protein that belongs to the tumor necrosis factor (TNF) family. It plays a crucial role in the regulation of the immune system and the induction of apoptosis, or programmed cell death. FasL is primarily expressed on the surface of activated T cells and natural killer cells, and it interacts with its receptor, Fas receptor (FasR), to trigger apoptotic signaling pathways.

Structure

Fas ligand is a homotrimeric protein, meaning it forms a complex of three identical subunits. Each subunit consists of an extracellular domain, a transmembrane domain, and a short cytoplasmic tail. The extracellular domain is responsible for binding to the Fas receptor, initiating the apoptotic cascade.

Function

The primary function of Fas ligand is to induce apoptosis in target cells. This is a critical mechanism for maintaining immune homeostasis and preventing autoimmune diseases. When FasL binds to FasR on the surface of a target cell, it triggers a series of intracellular events that lead to cell death. This process is essential for the elimination of infected or cancerous cells and for the termination of immune responses.

Role in Immune System

Fas ligand is involved in several key processes within the immune system:

  • Activation-Induced Cell Death (AICD): FasL is crucial for AICD, a process that helps regulate the immune response by eliminating excess lymphocytes after an immune response.
  • Peripheral Tolerance: FasL contributes to peripheral tolerance by inducing apoptosis in self-reactive T cells, thus preventing autoimmunity.
  • Cytotoxic T Lymphocyte (CTL) Function: CTLs use FasL to kill target cells, such as virus-infected cells or tumor cells, by inducing apoptosis.

Pathology

Dysregulation of Fas ligand or its receptor can lead to various diseases:

  • Autoimmune Diseases: Insufficient FasL activity can result in the survival of self-reactive lymphocytes, contributing to autoimmune conditions such as systemic lupus erythematosus and rheumatoid arthritis.
  • Cancer: Some cancer cells evade immune surveillance by downregulating FasR or expressing FasL to induce apoptosis in attacking immune cells.
  • Immunodeficiency: Mutations in the Fas or FasL genes can lead to immunodeficiency syndromes, characterized by lymphoproliferation and increased susceptibility to infections.

Clinical Applications

Understanding the Fas/FasL system has implications for therapeutic interventions:

  • Cancer Therapy: Strategies to enhance FasL-mediated apoptosis in tumor cells are being explored as potential cancer treatments.
  • Autoimmune Disease Treatment: Modulating FasL activity could help in treating autoimmune diseases by promoting the deletion of autoreactive lymphocytes.

Images

File:FasL structure.png
Diagram of Fas ligand structure showing its trimeric form.
File:FasL pathway.png
Illustration of the Fas/FasL apoptotic pathway.

Related pages