Patch grafting, strategies for transplantation of organoids into solid organs such as liver. (October 2021)
- Record Type:
- Journal Article
- Title:
- Patch grafting, strategies for transplantation of organoids into solid organs such as liver. (October 2021)
- Main Title:
- Patch grafting, strategies for transplantation of organoids into solid organs such as liver
- Authors:
- Zhang, Wencheng
Lanzoni, Giacomo
Hani, Homayoun
Overi, Diletta
Cardinale, Vincenzo
Simpson, Sean
Pitman, Wendy
Allen, Amanda
Yi, Xianwen
Wang, Xicheng
Gerber, David
Prestwich, Glenn
Lozoya, Oswaldo
Gaudio, Eugenio
Alvaro, Domenico
Tokaz, Debra
Dominguez-Bendala, Juan
Adin, Christopher
Piedrahita, Jorge
Mathews, Kyle
Sethupathy, Praveen
Carpino, Guido
He, Zhiying
Wauthier, Eliane
Reid, Lola M. - Abstract:
- Abstract: Epithelial cell therapies have been at an impasse because of inefficient methods of transplantation to solid organs. Patch grafting strategies were established enabling transplantation of ≥10 7th organoids/patch of porcine GFP+ biliary tree stem/progenitors into livers of wild type hosts. Grafts consisted of organoids embedded in soft (~100 Pa) hyaluronan hydrogels, both prepared in serum-free Kubota's Medium; placed against target sites; covered with a silk backing impregnated with more rigid hyaluronan hydrogels (~700 Pa); and use of the backing to tether grafts with sutures or glue to target sites. Hyaluronan coatings (~200–300 Pa) onto the serosal surface of the graft served to minimize adhesions with neighboring organs. The organ's clearance of hyaluronans enabled restoration of tissue-specific paracrine and systemic signaling, resulting in return of normal hepatic histology, with donor parenchymal cells uniformly integrated amidst host cells and that had differentiated to mature hepatocytes and cholangiocytes. Grafts containing donor mature hepatocytes, partnered with endothelia, and in the same graft biomaterials as for stem/progenitor organoids, did not engraft. Engraftment occurred if porcine liver-derived mesenchymal stem cells (MSCs) were co-transplanted with donor mature cells. RNA-seq analyses revealed that engraftment correlated with expression of matrix-metalloproteinases (MMPs), especially secreted isoforms that were found expressed strongly byAbstract: Epithelial cell therapies have been at an impasse because of inefficient methods of transplantation to solid organs. Patch grafting strategies were established enabling transplantation of ≥10 7th organoids/patch of porcine GFP+ biliary tree stem/progenitors into livers of wild type hosts. Grafts consisted of organoids embedded in soft (~100 Pa) hyaluronan hydrogels, both prepared in serum-free Kubota's Medium; placed against target sites; covered with a silk backing impregnated with more rigid hyaluronan hydrogels (~700 Pa); and use of the backing to tether grafts with sutures or glue to target sites. Hyaluronan coatings (~200–300 Pa) onto the serosal surface of the graft served to minimize adhesions with neighboring organs. The organ's clearance of hyaluronans enabled restoration of tissue-specific paracrine and systemic signaling, resulting in return of normal hepatic histology, with donor parenchymal cells uniformly integrated amidst host cells and that had differentiated to mature hepatocytes and cholangiocytes. Grafts containing donor mature hepatocytes, partnered with endothelia, and in the same graft biomaterials as for stem/progenitor organoids, did not engraft. Engraftment occurred if porcine liver-derived mesenchymal stem cells (MSCs) were co-transplanted with donor mature cells. RNA-seq analyses revealed that engraftment correlated with expression of matrix-metalloproteinases (MMPs), especially secreted isoforms that were found expressed strongly by organoids, less so by MSCs, and minimally, if at all, by adult cells. Engraftment with patch grafting strategies occurred without evidence of emboli or ectopic cell distribution. It was successful with stem/progenitor organoids or with cells with a source(s) of secreted MMP isoforms and offers significant potential for enabling cell therapies for solid organs. … (more)
- Is Part Of:
- Biomaterials. Volume 277(2021)
- Journal:
- Biomaterials
- Issue:
- Volume 277(2021)
- Issue Display:
- Volume 277, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 277
- Issue:
- 2021
- Issue Sort Value:
- 2021-0277-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-10
- Subjects:
- Liver -- Biliary tree -- Stem/progenitors -- Cell therapies -- Grafting -- Matrix-metalloproteinases (MMPs) -- Hyaluronans
Biomedical materials -- Periodicals
Biocompatible Materials -- Periodicals
Biomatériaux -- Périodiques
610.28 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01429612 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01429612 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01429612 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.biomaterials.2021.121067 ↗
- Languages:
- English
- ISSNs:
- 0142-9612
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2087.715000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 19167.xml