Perfusion-decellularization of vascularized pig stomachs

Maistriaux, Louis;Fievé, Lies;Vincent, Shirley;Gianello, Pierre;DUISIT, Jérôme;et.al.
(2019) 19th Congress of the European Society for Organ Transplantation — Location: Copenhagen, Denmark (15.September.2019)

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Authors
  • Author
  • Fievé, LiesUCLouvain
    Author
  • Vincent, ShirleyUCLouvain
    Author
  • Gianello, Pierreorcid-logoUCLouvain
    Author
  • Author
  • DUISIT, Jérômeorcid-logoUCLouvain
    Author
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Abstract
Background Total-partial gastrectomy, congenital gastric malformations and other causes of permanent gastric size reduction may result in severe side effects and poor life quality. A bioengineered stomach transplant could thus restore a physiological transit and a digestive function, while being fully compatible. This work aim was to apply, in piglet stomachs, the “decellularization-recellularization” approach, as previously reported by our team in human and porcine composite tissues. Methods/Materials Seven neonatal porcine stomachs were surgically harvested along with their vascular pedicle and decellularized by sequential perfusion of demineralized water, sodium dodecyl sulfate, Triton X-100, finalized by DNASe and PBS solutions.Cell clearance was evaluated by H&E and DAPI stainging and DNA quantification. Extracellular matrix preservation was assessed by Masson’s Trichrome (MT), type I and type IV collagens, and laminin stainings, elastin and GAG quantification. The vascular network was evaluated with angio-CT. Finally, matrix samples were sterilized and cultured with a fibroblastic cell line and analyzed by H&E and Live/dead stainings. Results Stomachs were successfully decellularized, with a fast bleaching during the SDS perfusion while preserving their morphology. Nuclei were absent on H&E, MT and DAPI staining; DNA reduction was significant (p<0.01). MT showed a well-preserved microscopic architecture of the mucosa, submucosa, muscularis and serosa layers. Type I, type IV collagens, and laminin were positively stained in both native and decellularized stomachs. Matrix proteins quantification revealed an increase for the collagen but a decrease for elastin and GAG. The angio-CT showed a well preserved and accessible vascular bed. Seeded fibroblasts were viable after 7 and 14 days, as shown by the Live/dead and the H&E stainings. Conclusion We demonstrated the ability to produce porcine stomach extracellular matrix with a preserved vascularization. This could offer broad new perspectives in organ tissue engineering at this anatomical level.
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Maistriaux, L., Fievé, L., Vincent, S., Gianello, P., Lengelé, B., & DUISIT, J. (2019). Perfusion-decellularization of vascularized pig stomachs. Transplant International, 32(Supplement 2), 422. https://hdl.handle.net/2078.5/94158 (Original work published 2019)