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Recipient cell surface molecules

Molecular classification
Receptor, Membrane protein, Lipopolysaccharide (bacteria), Glycoprotein, Ion channel, Adhesion molecule, Other (various molecules depending on context)
01

Overview

Recipient cell surface molecules encompass a diverse and context-dependent collection of membrane-bound proteins, glycoproteins, lipids, and polysaccharides found on the surface of cells that act as points of interaction for extracellular entities. In mammalian systems, these include broad classes such as receptors (GPCRs, tyrosine kinases, cytokine receptors), ion channels, and adhesion molecules involved in signal transduction, vesicle uptake, and cell-cell communication[2][1][4]. In microbial contexts, specific outer membrane proteins, lipopolysaccharides, and polysaccharides serve as receptors for conjugation machinery and horizontal transfer of genetic material[5][6]. These molecules are not a single target but represent a functional group essential for processes like extracellular vesicle uptake, immune modulation, and microbial gene transfer[1][2][5]. This term should not be used as a canonical entry for a therapeutic target; rather, individual surface molecules (such as “Programmed cell death protein 1,” “CD44,” “OmpA,” etc.) should be referenced and structured for database use[3][5][6].

Other names
cell surface moleculecell surface receptorrecipient membrane proteinconjugation receptorexofacial marker
02

Mechanism of action

Uptake of extracellular vesicles via fusion or endocytosis; Receptor-ligand binding leading to signal transduction; Adhesin-receptor interaction in bacterial conjugation

03

Biological functions

Signal transductionCellular uptake of extracellular vesiclesCell-cell communicationImmune responseHorizontal gene transfer (in bacteria)Regulation of cell behaviorOther
04

Disease associations

Cancer (via EV-mediated regulation)Infection (bacterial conjugation)Immune modulationInflammationOther (context-dependent)
05

Safety considerations

Off-target effects if non-specific targeting is attemptedImmunogenicity of cell surface molecules in therapyRisk of facilitating unwanted cell-cell transfer (e.g., horizontal gene transfer in bacteria)Potential for modulating immune response undesirably
06

Biomarkers

CD markers (CD29, CD44, CD73, CD90, CD105, CD117 for EVs)Disease-specific EV surface protein markersNot applicable as a class—must specify molecule

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