Precision cell delivery in biphasic polymer systems enhances growth of keratinocytes in culture and promotes their attachment on acellular dermal matrices

Rishima Agarwal, Guanyong Liu, Nicky W. Tam, Paul F. Gratzer, John P. Frampton

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

7 Citas (Scopus)

Resumen

Current approaches for precision deposition of cells are not optimized for moist environments or for substrates with complex surface topographic features, for example, the surface of dermal matrices and other biomaterials. To overcome these challenges, an approach is presented that utilizes cell confinement in phase-separating polymer solutions of polyethylene glycol and dextran to precisely deliver keratinocytes in well-defined colonies. Using this approach, keratinocyte colonies are produced with superior viability, proliferative capacity, and barrier formation compared with the same number of cells dispersedly seeded across substrate surfaces. It is further demonstrated that keratinocytes delivered in colonies to the surface of acellular dermal matrices form an intact epidermal basal layer more rapidly and more completely than cells delivered by conventional dispersed seeding. These findings demonstrate that delivery of keratinocytes in phase-separating polymer solutions holds potential for enhancing growth of keratinocytes in culture and production of functional skin equivalents.

Idioma originalEnglish
Páginas (desde-hasta)997-1006
Número de páginas10
PublicaciónJournal of Tissue Engineering and Regenerative Medicine
Volumen13
N.º6
DOI
EstadoPublished - jun. 2019

Nota bibliográfica

Funding Information:
Natural Sciences and Engineering Research Council of Canada, Grant/Award Number: RGPIN‐2016‐02498

Funding Information:
We wish to thank DeCell Technologies for providing DermGEN™ samples for this study. R. A. acknowledges scholarships from the Canadian Institutes of Health Research (CIHR) and the Dalhousie University Faculty of Engineering (Exxon Mobil Canada Ltd.). N. W. T. acknowledges scholarship from the Dalhousie University Faculty of Medicine (Graduate Studentship Award). This work was supported by Canada Research Chairs Program, Canada Foundation for Innovation (Project# 33533), and the Natural Sciences and Engineering Research Council of Canada (NSERC–RGPIN‐2016‐02498).

Funding Information:
We wish to thank DeCell Technologies for providing DermGEN™ samples for this study. R. A. acknowledges scholarships from the Canadian Institutes of Health Research (CIHR) and the Dalhousie University Faculty of Engineering (Exxon Mobil Canada Ltd.). N. W. T. acknowledges scholarship from the Dalhousie University Faculty of Medicine (Graduate Studentship Award). This work was supported by Canada Research Chairs Program, Canada Foundation for Innovation (Project# 33533), and the Natural Sciences and Engineering Research Council of Canada (NSERC–RGPIN-2016-02498).

Publisher Copyright:
© 2019 John Wiley & Sons, Ltd.

ASJC Scopus Subject Areas

  • Medicine (miscellaneous)
  • Biomaterials
  • Biomedical Engineering

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