Vitronectin-Mediated Cell Interaction Mechanisms

Summary

Vitronectin is a multifunctional glycoprotein present in plasma and deposited within the extracellular matrix, where it orchestrates a suite of cellular behaviours through interactions with cell-surface receptors and matrix components. Central to its activity is the RGD (Arg-Gly-Asp) motif, which engages integrin receptors—particularly αvβ3 and αvβ5—to regulate cell adhesion, spreading and migration. Conformational rearrangements expose cryptic binding domains for protease inhibitors and glycosaminoglycans, thereby modulating fibrinolysis, coagulation and tissue remodelling. Beyond its adhesive roles, vitronectin acts as a signalling scaffold: binding to integrins recruits focal adhesion kinase and downstream effectors such as STAT3 to sustain mitochondrial bioenergetics and promote cell survival. In the nervous system, vitronectin–integrin engagement supports neurite outgrowth, preserves blood–brain barrier integrity and may influence neurodegenerative processes. Through its versatility in receptor recognition, vitronectin underpins wound healing, angiogenesis and stem-cell maintenance, making it a focal point for therapeutic strategies in tissue regeneration, cancer metastasis and neuroprotection.

Research from Nature Portfolio

No recent Nature Portfolio content available.

Vitronectin-Mediated Cell Interaction Mechanisms publication trend

The graph below shows the total number of articles in vitronectin-mediated cell interaction mechanisms across all publications each year (not limited to Nature Index journals).

Technical terms

RGD motif: A tripeptide sequence (Arg-Gly-Asp) in vitronectin that binds integrin receptors to mediate cell adhesion.

Integrin: A family of transmembrane heterodimeric receptors that connect extracellular ligands to intracellular cytoskeletal and signalling networks.

Glycosaminoglycan (GAG): A linear polysaccharide chain, such as heparin, that associates with vitronectin to regulate its conformation and multimerisation.

Somatomedin B domain: A compact N-terminal region of vitronectin that binds plasminogen activator inhibitor-1 and contributes to cell-surface receptor interactions.

Focal adhesion kinase (FAK): A cytoplasmic tyrosine kinase activated by integrin clustering that links adhesion receptors to downstream survival and growth pathways.

References

  1. Integrin-FAK signaling rapidly and potently promotes mitochondrial function through STAT3. Cell Communication and Signaling (2016).
  2. Role of Vitronectin and Its Receptors in Neuronal Function and Neurodegenerative Diseases. International Journal of Molecular Sciences (2022).
  3. The Solution Structure of the N-terminal Domain of Human Vitronectin PROXIMAL SITES THAT REGULATE FIBRINOLYSIS AND CELL MIGRATION*. Journal of Biological Chemistry (2004).

About these summaries

This Nature Research Intelligence Topic summary is created with the cited references and a large language model. We take care to ground generated text with facts, and have systems in place to gain human feedback on the overall quality of the process in line with our AI principles. We strive to create accurate and useful summaries for people unfamiliar with the research topic and that supports this goal. These pages are a beta release and will be updated as we learn how best to help people gain value from a research topic summary.

Nature Strategy Reports
Turn complex research questions into confident strategic decisions 

When you're under pressure to set direction, justify investment, or understand your competitive position, you need more than raw data — you need trusted insights you can act on.

  • Benchmark your performance against global peers using robust, methodologically sound analysis.

  • Combine quantitative metrics with qualitative expert insight to uncover strengths, gaps and emerging opportunities.

  • Gain tailored, decision-ready recommendations aligned to your strategic priorities.

Talk to us to learn more about our data dashboards and bespoke strategy reports.

Nature Masterclasses
Grow research skills, confidence and careers with training built for every stage of the research lifecycle.

Developed with Nature Portfolio journal Editors and internationally renowned experts. Discover three ways to learn:

  • Self-paced, online courses in convenient bite-sized units, covering key skills across scientific writing, publishing, grant writing, data analysis, and more.

  • Expert trainer-led workshops with hands-on exercises and real-time feedback across core research skills, delivered via interactive group sessions.

  • Editor-led workshops combining core principles in writing and publishing, personalised 1:1 feedback from Nature Portfolio Editors and hands-on exercises.

Explore course catalogues and workshop agendas, enquire about the options or request institutional pricing.