EMR2
EMR2, or Egf-Like Module Containing, Mucin-Like, Hormone Receptor-Like 2, is a protein that in humans is encoded by the EMR2 gene. This gene is a member of the adhesion G protein-coupled receptor (GPCR) family. Adhesion GPCRs are a large family of G protein-coupled receptors that play a critical role in various biological processes including cell adhesion, immune response, and neurodevelopment. EMR2, in particular, has been implicated in the regulation of inflammatory responses and immune system functions.
Structure
EMR2 is characterized by an extended extracellular region containing multiple EGF-like domains, which are typical for proteins involved in cell adhesion and signaling. The extracellular domain is followed by a seven-transmembrane domain, characteristic of GPCRs, which transduces signals across the cell membrane. The N-terminal fragment of EMR2 is rich in cysteine residues, forming the EGF-like domains that are crucial for its interaction with other molecules and possibly for its ligand-binding specificity.
Function
The precise biological functions of EMR2 are still being elucidated. However, it is known to play a role in the modulation of immune responses. EMR2 expression is predominantly found in myeloid cells, such as monocytes and macrophages, where it can influence the cell's behavior in response to inflammation. It has been suggested that EMR2 can mediate cell adhesion and migration, processes essential for the immune system's response to injury and infection. Additionally, EMR2 may participate in the regulation of cytokine production, further influencing inflammatory responses.
Clinical Significance
Alterations in the expression or function of EMR2 have been associated with various inflammatory and autoimmune diseases. Given its role in modulating immune responses, EMR2 is a potential target for therapeutic interventions in conditions characterized by excessive or inappropriate inflammation. Research into EMR2's involvement in specific diseases is ongoing, with the aim of developing novel treatments that can modulate its activity.
Research Directions
Future research on EMR2 is likely to focus on elucidating its ligand specificity, signaling pathways, and the mechanisms by which it regulates immune responses. Understanding these aspects of EMR2 function could reveal new therapeutic targets for a range of inflammatory and autoimmune diseases. Additionally, studies are needed to explore the potential of targeting EMR2 in cancer therapy, given the importance of immune regulation in tumor progression and response to treatment.
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Contributors: Prab R. Tumpati, MD