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Gene regulation of intracellular adhesion molecule-1 (ICAM-1): A molecule with multiple functions
- Source :
- Immunology Letters. 240:123-136
- Publication Year :
- 2021
- Publisher :
- Elsevier BV, 2021.
-
Abstract
- Intracellular adhesion molecule 1 (ICAM-1) is one of the most extensively studied inducible cell adhesion molecules which is responsible for several immune functions like T cell activation, extravasation, inflammation, etc. The molecule is constitutively expressed over the cell surface and is regulated up / down in response to inflammatory mediators like cellular stress, proinflammatory cytokines, viral infection. These stimuli modulate the expression of ICAM-1 primarily through regulating the ICAM-1 gene transcription. On account of the presence of various binding sites for NF-κB, AP-1, SP-1, and many other transcription factors, the architecture of the ICAM-1 promoter become complex. Transcription factors in union with other transcription factors, coactivators, and suppressors promote their assembly in a stereospecific manner on ICAM-1 promoter which mediates ICAM-1 regulation in response to different stimuli. Along with transcriptional regulation, epigenetic modifications also play a pivotal role in controlling ICAM-1 expression on different cell types. In this review, we summarize the regulation of ICAM-1 expression both at the transcriptional as well as post-transcriptional level with an emphasis on transcription factors and signaling pathways involved.
- Subjects :
- Regulation of gene expression
Transcription, Genetic
Chemistry
Cell adhesion molecule
T-Lymphocytes
Immunology
Intercellular Adhesion Molecule-1
Lymphocyte Activation
Response Elements
Proinflammatory cytokine
Cell biology
Gene Expression Regulation
Transcriptional regulation
Humans
Immunology and Allergy
Epigenetics
Signal transduction
Transcription factor
Intracellular
Signal Transduction
Transcription Factors
Subjects
Details
- ISSN :
- 01652478
- Volume :
- 240
- Database :
- OpenAIRE
- Journal :
- Immunology Letters
- Accession number :
- edsair.doi.dedup.....ec373028cb1d9567b4796f498be80d6f