Evaluation of transplantation sites for human intestinal organoids.
Akaljot SinghHolly M PolingNambirajan SundaramNicole BrownJames M WellsMichael A HelmrathPublished in: PloS one (2020)
Our group has developed two transplantation models for the engraftment of Human Intestinal Organoids (HIOs): the renal subcapsular space (RSS) and the mesentery each with specific benefits for study. While engraftment at both sites generates laminated intestinal structures, a direct comparison between models has not yet been performed. Embryonic stem cells were differentiated into HIOs, as previously described. HIOs from the same batch were transplanted on the same day into either the RSS or mesentery. 10 weeks were allowed for engraftment and differentiation, at which time they were harvested and assessed. Metrics for comparison included: mortality, engraftment rate, gross size, number and grade of lumens, and expression of markers specific to epithelial differentiation, mesenchymal differentiation, and carbohydrate metabolism. Mortality was significantly increased when undergoing mesentery transplantation, however engraftment was significantly higher. Graft sizes were similar between groups. Morphometric parameters were similar between groups, however m-tHIOs presented with significantly fewer lumens than k-tHIO. Transcript and protein level expression of markers specific to epithelial differentiation, mesenchymal differentiation, and carbohydrate metabolism were similar between groups. Transplantation into both sites yields viable tissue of similar quality based on our assessments with enhanced engraftment and a dominant lumen for uniform study benefiting the mesenteric site and survival benefiting RSS.
Keyphrases
- hematopoietic stem cell
- endothelial cells
- poor prognosis
- induced pluripotent stem cells
- stem cells
- bone marrow
- cell therapy
- cardiovascular events
- binding protein
- risk factors
- high resolution
- long non coding rna
- pluripotent stem cells
- type diabetes
- mesenchymal stem cells
- coronary artery disease
- amino acid
- mass spectrometry
- small molecule
- quality improvement
- children with cerebral palsy
- preterm birth
- free survival