# Biofunctionalized Vascular Access Graft Improves Patency and Endothelialization in a Porcine Arteriovenous Model

**Authors:** Aurora Battistella, Morgan Linger, Meredith Overton, Unimunkh Uriyanghai, Christine Wai, Gang Xi, Prabir Roy-Chaudhury, Wei Tan

PMC · DOI: 10.3390/jfb17020065 · 2026-01-27

## TL;DR

A new vascular graft was developed that supports tissue regeneration and maintains mechanical strength in a pig model for hemodialysis.

## Contribution

The study introduces a reinforced, biofunctionalized graft that enables in situ endothelialization and extracellular matrix remodeling in a large animal model.

## Key findings

- The graft showed mechanical properties comparable to Gore-Tex PTFE, including kink resistance and burst pressure.
- In vivo, the graft supported host cell infiltration, collagen deposition, and smooth muscle-like tissue formation.
- Multiphoton imaging revealed greater collagen and elastin content in the graft compared to PTFE controls.

## Abstract

Reliable vascular access remains a major clinical challenge for hemodialysis patients, as expanded polytetrafluoroethylene (PTFE) grafts exhibit poor patency and frequent complications driven by thrombosis and neointimal hyperplasia. Tissue-engineered vascular grafts offer a regenerative alternative but often lack the mechanical resilience required for high-flow arteriovenous (AV) environments. Here, we developed a reinforced, biofunctionalized coaxial electrospun graft comprising a poly(ε-caprolactone) mechanical core and a norbornene-functionalized poly(ethylene glycol) sheath incorporating pro-endothelialization cues. Circumferential PTFE rings were added to improve kink resistance. Grafts were implanted in a porcine AV configuration that recapitulates clinical hemodynamic conditions. Mechanical characterization included compliance, burst pressure, and kink resistance; host remodeling was assessed using histology, immunofluorescence, and multiphoton imaging at 4 weeks. Ring-reinforced electrospun grafts demonstrated a kink radius of 0.187 cm, compliance of 1.04 ± 0.29%/100 mmHg, and burst pressure of 1505 ± 565 mmHg, values all comparable to Gore-Tex PTFE and within industrial performance standards. In vivo, the electrospun grafts showed extensive host cell infiltration, collagen deposition, and formation of smooth muscle-like tissue, whereas PTFE controls remained largely acellular. Immunofluorescence confirmed intramural α-SMA+ and CD31+ cell populations, and multiphoton microscopy revealed significantly greater collagen and elastin content compared with PTFE (p < 0.05). Collectively, these findings demonstrate that the reinforced electrospun graft maintains mechanical integrity under physiological AV loading while supporting in situ endothelialization and extracellular matrix remodeling in a clinically relevant, large animal model. This work provides one of the first demonstrations of functional tissue regeneration within a fully synthetic, acellular scaffold in a porcine hemodialysis model and advances the translational development of durable, regenerative vascular access grafts that couple mechanical resilience with bioactive healing capacity.

## Linked entities

- **Proteins:** ACTA1 (actin alpha 1, skeletal muscle), PECAM1 (platelet and endothelial cell adhesion molecule 1)
- **Chemicals:** poly(ethylene glycol) (PubChem CID 9033), norbornene (PubChem CID 638051), doxorubicin (PubChem CID 31703)

## Full-text entities

- **Genes:** ELN (elastin) [NCBI Gene 2006] {aka ADCL1, SVAS, WBS, WS}, PECAM1 (platelet and endothelial cell adhesion molecule 1) [NCBI Gene 5175] {aka CD31, CD31/EndoCAM, GPIIA', PECA1, PECAM-1, endoCAM}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, SMN1 (survival of motor neuron 1, telomeric) [NCBI Gene 6606] {aka BCD541, GEMIN1, SMA, SMA1, SMA2, SMA3}, ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58] {aka ACTA, ASMA, CFTD, CFTD1, CFTDM, CMYO2A}
- **Diseases:** infection (MESH:D007239), ESKD (MESH:D007676), vascular calcification (MESH:D061205), thrombosis (MESH:D013927), hypertension (MESH:D006973), occlusions (MESH:D001157), neointimal hyperplasia (MESH:D006965), Kink Resistance (MESH:D060467), diabetes (MESH:D003920), uremia (MESH:D014511), inflammatory (MESH:D007249), injury to (MESH:D014947), stenosis (MESH:D003251)
- **Chemicals:** thiol (MESH:D013438), PCL (MESH:C016240), Alexa Fluor 488 (MESH:C000711379), Alexa Fluor (-), H&amp;E (MESH:D006371), Hematoxylin (MESH:D006416), RGD (MESH:C047981), Eosin-Y (MESH:D004801), Buprenorphine (MESH:D002047), heparin (MESH:D006493), alcohols (MESH:D000438), DAPI (MESH:C007293), formalin (MESH:D005557), Maleimide (MESH:C043592), Irgacure 2959 (MESH:C499598), cysteine (MESH:D003545), Prolene (MESH:D011126), PEG dithiol (MESH:C535242), PEG (MESH:D011092), DATS (MESH:C042577), polymer (MESH:D011108), cyanoacrylate (MESH:D003487), paraffin (MESH:D010232), midazolam (MESH:D008874), Dexon (MESH:C007287), stainless steel (MESH:D013193), PTFE (MESH:D011138), oxygen (MESH:D010100), propofol (MESH:D015742), Norbornene (MESH:C046060), Hexafluoroisopropanol (MESH:C001337), ethanol (MESH:D000431), water (MESH:D014867), aspirin (MESH:D001241), isoflurane (MESH:D007530), peptides (MESH:D010455)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Sus scrofa (pig, species) [taxon 9823]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941732/full.md

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Source: https://tomesphere.com/paper/PMC12941732