Target intelligence / Profile preview

Endothelial microparticle (EMP)

Target
EMP
Molecular classification
Extracellular vesicle, Cell-derived microparticle, Other
01

Overview

Endothelial microparticles (EMPs) are submicron extracellular vesicles, typically ranging from 100 nm to 1 μm in diameter, that are shed from the plasma membrane of endothelial cells in response to activation, injury, or apoptosis. They represent a specialized subset of endothelial-derived factors that act as mobile biological effectors, carrying a complex cargo of proteins, lipids, and genetic material, such as microRNAs, to target cells. In healthy physiological states, they participate in vascular homeostasis and cell-to-cell communication; however, their levels are significantly elevated in conditions characterized by endothelial dysfunction, including cardiovascular disease, diabetes mellitus, and systemic inflammation. EMPs are increasingly recognized as both diagnostic biomarkers for disease progression and potential therapeutic targets, with research focusing on pharmacological interventions that can reduce their shedding or block their pro-inflammatory and pro-thrombotic effects on the vasculature.

Other names
Endothelial-derived microparticleEndothelial-derived microvesicleEndothelial extracellular vesicleEndothelial-derived factorEndothelial-derived microparticle (EMP)
02

Mechanism of action

Reduction of endothelial cell activation and apoptosis to decrease the shedding of microparticles; inhibition of microparticle-mediated pro-inflammatory and pro-coagulant signaling pathways.

03

Biological functions

Signal transductionCoagulationInflammationAngiogenesisCell-to-cell communicationApoptosis
04

Disease associations

Cardiovascular diseaseDiabetes mellitusSepsisInflammationChronic obstructive pulmonary diseaseHypertensionAtherosclerosis
05

Safety considerations

Potential for systemic disruption of physiological intercellular communicationLack of standardized isolation and quantification protocolsHigh heterogeneity in vesicle cargo and surface markersPotential off-target effects when used as delivery vehicles
06

Interacting drugs

Atorvastatin

5 more in the full profile.

07

Biomarkers

CD31 (PECAM-1)CD144 (VE-cadherin)CD62E (E-selectin)CD146 (MCAM)CD105 (Endoglin)Annexin V

Beyond the preview

Go deeper on Endothelial microparticle (EMP).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Endothelial microparticle (EMP).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call