Related Experiment Video
Updated: Mar 20, 2026

Induction of Adhesion-dependent Signals Using Low-intensity Ultrasound
Published on: May 8, 2012
Syndecan-4, a PRRSV attachment factor, mediates PRRSV entry through its interaction with EGFR
1College of Veterinary Medicine, Nanjing Agricultural University, China.
Abstract:
The causative agent of porcine reproductive and respiratory syndrome is the PRRS virus (PRRSV), an enveloped, single-stranded and positive-sense RNA virus. The host factors and mechanisms that are involved in PRRSV entry are still largely unknown. In our present studies, we found that syndecan-4, one of the heparan sulfate proteoglycans, plays a critical role in PRRSV entry, especially in PRRSV attachment. Moreover, EGFR interacts with syndecan-4 in MACR-145 cells and disruption of their interaction impaired PRRSV entry. Furthermore, EGFR inhibitor AG1478 or syndecan-4 derived peptide SSTN87-131 inhibited syndecan-4 endocytosis induced by PRRSV entry. Altogether, syndecan-4, a PRRSV attachment factor, mediated PRRSV entry by interacting with EGFR.
Insights
Syndecan-4 is crucial for Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) entry by acting as an attachment factor. It interacts with EGFR, mediating viral entry into host cells.
Area of Science:
- Virology
- Cell Biology
- Biochemistry
Background:
- Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) causes significant economic losses in the swine industry.
- Understanding PRRSV entry mechanisms is vital for developing effective control strategies.
- Host factors mediating PRRSV cell entry remain largely unidentified.
Purpose of the Study:
- To investigate host factors involved in PRRSV cell entry.
- To elucidate the role of syndecan-4 in PRRSV attachment and entry.
- To explore the interaction between syndecan-4 and Epidermal Growth Factor Receptor (EGFR) during PRRSV infection.
Main Methods:
- Utilized MACR-145 cells for PRRSV infection studies.
- Investigated the role of syndecan-4 using specific peptides and inhibitors.
- Assessed the interaction between syndecan-4 and EGFR.
- Monitored PRRSV entry and syndecan-4 endocytosis.
Main Results:
- Syndecan-4, a heparan sulfate proteoglycan, was identified as a critical factor for PRRSV attachment and entry.
- EGFR was found to interact with syndecan-4 in MACR-145 cells, and disrupting this interaction inhibited PRRSV entry.
- Inhibition of EGFR or syndecan-4 function impaired PRRSV-induced syndecan-4 endocytosis.
Conclusions:
- Syndecan-4 acts as a PRRSV attachment factor, mediating viral entry.
- The interaction between syndecan-4 and EGFR is essential for efficient PRRSV cell entry.
- Targeting the syndecan-4/EGFR pathway may offer a novel strategy to block PRRSV infection.
Related Concept Videos
Intracellular Signaling Affects Focal Adhesions
Some...
Adherens Junctions
Adherens Junctions are Dynamic
Fibronectins Connect Cells with ECM
Both proteoglycans and collagen are attached to fibronectin proteins, which, in turn, are attached to integrin proteins. These integrin proteins interact with transmembrane...
Mitogens and the Cell Cycle
Rous Sarcoma Virus (RSV) and Cancer
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
Rous Sarcoma Virus (RSV) and Cancer

