| Literature DB >> 30548802 |
Katja Jansen1, Miguel Castilho2,3, Sanne Aarts1,2, Michael M Kaminski4, Soeren S Lienkamp4, Roman Pichler4, Jos Malda2,3,5, Tina Vermonden1,6,3, Jitske Jansen7, Rosalinde Masereeuw1,3.
Abstract
The increasing prevalence of end-stage renal disease and persistent shortage of donor organs call for alternative therapies for kidney patients. Dialysis remains an inferior treatment as clearance of large and protein-bound waste products depends on active tubular secretion. Biofabricated tissues could make a valuable contribution, but kidneys are highly intricate and multifunctional organs. Depending on the therapeutic objective, suitable cell sources and scaffolds must be selected. This study provides a proof-of-concept for stand-alone kidney tubule grafts with suitable mechanical properties for future implantation purposes. Porous tubular nanofiber scaffolds are fabricated by electrospinning 12%, 16%, and 20% poly-ε-caprolactone (PCL) v/w (chloroform and dimethylformamide, 1:3) around 0.7 mm needle templates. The resulting scaffolds consist of 92%, 69%, and 54% nanofibers compared to microfibers, respectively. After biofunctionalization with L-3,4-dihydroxyphenylalanine and collagen IV, 10 × 106 proximal tubule cells per mL are injected and cultured until experimental readout. A human-derived cell model can bridge all fiber-to-fiber distances to form a monolayer, whereas small-sized murine cells form monolayers on dense nanofiber meshes only. Fabricated constructs remain viable for at least 3 weeks and maintain functionality as shown by inhibitor-sensitive transport activity, which suggests clearance capacity for both negatively and positively charged solutes.Entities:
Keywords: polycaprolactone; regenerative medicine; renal replacement therapy; renal transport; tissue engineering
Mesh:
Substances:
Year: 2018 PMID: 30548802 PMCID: PMC7116029 DOI: 10.1002/mabi.201800412
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979