Optimizing perfusion-decellularization methods of porcine livers for clinical-scale whole-organ bioengineering.

Abstract:

:Aim. To refine the decellularization protocol of whole porcine liver, which holds great promise for liver tissue engineering. Methods. Three decellularization methods for porcine livers (1% sodium dodecyl sulfate (SDS), 1% Triton X-100 + 1% sodium dodecyl sulfate, and 1% sodium deoxycholate + 1% sodium dodecyl sulfate) were studied. The obtained liver scaffolds were processed for histology, residual cellular content analysis, and extracellular matrix (ECM) components evaluation to investigate decellularization efficiency and ECM preservation. Rat primary hepatocytes were seeded into three kinds of scaffold to detect the biocompatibility. Results. The whole liver decellularization was successfully achieved following all three kinds of treatment. SDS combined with Triton had a high efficacy of cellular removal and caused minimal disruption of essential ECM components; it was also the most biocompatible procedure for primary hepatocytes. Conclusion. We have refined a novel, standardized, time-efficient, and reproducible protocol for the decellularization of whole liver which can be further adapted to liver tissue engineering.

journal_name

Biomed Res Int

authors

Wu Q,Bao J,Zhou YJ,Wang YJ,Du ZG,Shi YJ,Li L,Bu H

doi

10.1155/2015/785474

subject

Has Abstract

pub_date

2015-01-01 00:00:00

pages

785474

eissn

2314-6133

issn

2314-6141

journal_volume

2015

pub_type

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