Decellularization of kidney tissue: comparison of sodium lauryl ether sulfate and sodium dodecyl sulfate for allotransplantation in rat
Autor: | Sajad Daneshi, Mahdi Muhaddesi, Mohammad Reza Miri, Iraj Nabipour, Pouya Behrouzi, Mehdi Mahmudpour, Arezoo Khoradmehr, Mohammad Amin Keshvari, Alireza Afshar, Hossein Azari, Amin Tamadon, Reza Shirazi, Mandana Baghban |
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Rok vydání: | 2021 |
Předmět: |
Kidney
Histology Chromatography Decellularization Biocompatibility Chemistry Sodium Mesenchymal stem cell chemistry.chemical_element Cell Biology Pathology and Forensic Medicine Extracellular matrix Glycosaminoglycan chemistry.chemical_compound medicine.anatomical_structure medicine Sodium dodecyl sulfate |
Zdroj: | Cell and Tissue Research. 386:365-378 |
ISSN: | 1432-0878 0302-766X |
DOI: | 10.1007/s00441-021-03517-5 |
Popis: | An automatic decellularization device was developed to perfuse and decellularize male rats’ kidneys using both sodium lauryl ether sulfate (SLES) and sodium dodecyl sulfate (SDS) and to compare their efficacy in kidney decellularization and post-transplantation angiogenesis. Kidneys were perfused with either 1% SDS solution for 4 h or 1% SLES solution for 6 h. The decellularized scaffolds were stained with hematoxylin and eosin, periodic acid Schiff, Masson’s trichrome, and Alcian blue to determine cell removal and glycogen, collagen, and glycosaminoglycan contents, respectively. Moreover, scanning electron microscopy was performed to evaluate the cell removal and preservation of microarchitecture of both SDS and SLES scaffolds. Additionally, DNA quantification assay was applied for all groups in order to measure residual DNA in the scaffolds and normal kidney. In order to demonstrate biocompatibility of the decellularized scaffolds, human umbilical cord mesenchymal stromal/stem cells (hUC-MSCs) were seeded on the scaffolds. In addition, the allotransplantation was performed in back muscle and angiogenesis was evaluated. Complete cell removal in both SLES and SDS groups was observed in scanning electron microscopy and DNA quantification assays. Moreover, the extracellular matrix (ECM) architecture of rat kidney in the SLES group was significantly preserved better than the SDS group. The hUC-MSCs were successfully migrated from the cell culture plate surface into the SDS and SLES decellularized scaffolds. The formation of blood vessels was observed in the kidney in both SLES and SDS decellularized kidneys. The better preservation of ECM than SDS introduces SLES as the solvent of choice for kidney decellularization. |
Databáze: | OpenAIRE |
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