RELB
RELB is a member of the NF-kappa B family of transcription factors that play a critical role in inflammation, immune response, cell growth, and cell survival. The NF-kappa B/Rel family includes several structurally related proteins that form homodimers or heterodimers to function as transcription factors. These proteins include RELA (p65), c-Rel, NF-kappa B1 (p50 and its precursor p105), NF-kappa B2 (p52 and its precursor p100), and RELB. They are involved in the regulation of a wide variety of genes that control various biological processes.
Function
RELB forms heterodimers primarily with p50 and p52, which are processed forms of NF-kappa B1 and NF-kappa B2, respectively. Unlike other NF-kappa B members that are activated by a wide range of stimuli, RELB activation is mainly dependent on the non-canonical NF-kappa B pathway, which is triggered by specific signals such as lymphotoxin beta (LTβ) and BAFF (B-cell activating factor). This pathway involves the processing of NF-kappa B2 p100 to p52, leading to the release and nuclear translocation of RELB:p52 heterodimers.
The RELB:p52 complex regulates the expression of genes involved in the development and organization of secondary lymphoid organs, the differentiation of dendritic cells, and the regulation of immune responses, particularly those involving T cells and B cells. Its activity is crucial for the formation of germinal centers, which are key sites for the generation of high-affinity antibodies.
Clinical Significance
Alterations in the RELB pathway have been implicated in various autoimmune diseases, inflammatory disorders, and cancers. Due to its role in immune regulation, dysregulation of RELB can lead to either an inadequate immune response or excessive inflammation. In cancer, RELB can have dual roles, either promoting or inhibiting tumor growth and survival, depending on the context and type of tumor. This makes it a potential target for therapeutic interventions aimed at modulating the immune response or treating cancer.
Research
Research on RELB continues to uncover its complex role in the immune system and its potential as a therapeutic target. Studies are exploring how modulation of the RELB pathway can be used to treat autoimmune diseases, enhance vaccine efficacy, and improve cancer immunotherapy outcomes. Understanding the precise mechanisms of RELB action and its interactions with other signaling pathways is crucial for developing targeted therapies.
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Contributors: Prab R. Tumpati, MD