Cell engraftment, vascularization, and inflammation after treatment of equine distal limb wounds with endothelial colony forming cells encapsulated within hydrogel microspheres.


Journal

BMC veterinary research
ISSN: 1746-6148
Titre abrégé: BMC Vet Res
Pays: England
ID NLM: 101249759

Informations de publication

Date de publication:
04 Feb 2020
Historique:
received: 13 09 2019
accepted: 27 01 2020
entrez: 6 2 2020
pubmed: 6 2 2020
medline: 30 9 2020
Statut: epublish

Résumé

Endothelial colony forming cells (ECFCs) may be useful therapeutically in conditions with poor blood supply, such as distal limb wounds in the horse. Encapsulation of ECFCs into injectable hydrogel microspheres may ensure cell survival and cell localization to improve neovascularization and healing. Autologous ECFCs were isolated from 6 horses, labeled with quantum nanodots (QD), and a subset were encapsulated in poly(ethylene) glycol fibrinogen microspheres (PEG-Fb MS). Full-thickness dermal wounds were created on each distal limb and injected with empty PEG-Fb MS, serum, ECFCs, or ECFCs encapsulated into PEG- Fb MS (ECFC/MS). Analysis included wound surface area (WSA), granulation tissue scoring (GS), thermography, collagen density staining, and immunohistochemical staining for endothelial and inflammatory cells. The purpose of this study was to track cell location and evaluate wound vascularization and inflammatory response after injection of ECFC/MS or naked ECFCs in equine distal limb wounds. ECFCs were found near and within newly formed blood vessels up to 3 weeks after injection. ECFC and ECFC/MS groups had the greatest blood vessel quantity at week 1 in the wound periphery. Wounds treated with ECFCs and ECFC/MS had the lowest density of neutrophils and macrophages at week 4. There were no significant effects of ECFC or ECFC/MS treatment on other measured parameters. Injection of microsphere encapsulated ECFCs was practical for clinical use and well-tolerated. The positive ECFC treatment effects on blood vessel density and wound inflammation warrant further investigation.

Sections du résumé

BACKGROUND BACKGROUND
Endothelial colony forming cells (ECFCs) may be useful therapeutically in conditions with poor blood supply, such as distal limb wounds in the horse. Encapsulation of ECFCs into injectable hydrogel microspheres may ensure cell survival and cell localization to improve neovascularization and healing. Autologous ECFCs were isolated from 6 horses, labeled with quantum nanodots (QD), and a subset were encapsulated in poly(ethylene) glycol fibrinogen microspheres (PEG-Fb MS). Full-thickness dermal wounds were created on each distal limb and injected with empty PEG-Fb MS, serum, ECFCs, or ECFCs encapsulated into PEG- Fb MS (ECFC/MS). Analysis included wound surface area (WSA), granulation tissue scoring (GS), thermography, collagen density staining, and immunohistochemical staining for endothelial and inflammatory cells. The purpose of this study was to track cell location and evaluate wound vascularization and inflammatory response after injection of ECFC/MS or naked ECFCs in equine distal limb wounds.
RESULTS RESULTS
ECFCs were found near and within newly formed blood vessels up to 3 weeks after injection. ECFC and ECFC/MS groups had the greatest blood vessel quantity at week 1 in the wound periphery. Wounds treated with ECFCs and ECFC/MS had the lowest density of neutrophils and macrophages at week 4. There were no significant effects of ECFC or ECFC/MS treatment on other measured parameters.
CONCLUSIONS CONCLUSIONS
Injection of microsphere encapsulated ECFCs was practical for clinical use and well-tolerated. The positive ECFC treatment effects on blood vessel density and wound inflammation warrant further investigation.

Identifiants

pubmed: 32019556
doi: 10.1186/s12917-020-2269-y
pii: 10.1186/s12917-020-2269-y
pmc: PMC7001230
doi:

Substances chimiques

Hydrogels 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

43

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Auteurs

Randolph L Winter (RL)

Department of Clinical Sciences, Auburn University, Auburn, AL, USA.
Department of Clinical Sciences, Ohio State University, Columbus, OH, USA.

Yuan Tian (Y)

Department of Chemical Engineering, Auburn University, Auburn, AL, USA.

Fred J Caldwell (FJ)

Department of Clinical Sciences, Auburn University, Auburn, AL, USA.

Wen J Seeto (WJ)

Department of Chemical Engineering, Auburn University, Auburn, AL, USA.

Jey W Koehler (JW)

Department of Pathobiology, Auburn University, Auburn, AL, USA.

David A Pascoe (DA)

School of Kinesiology, Auburn University, Auburn, AL, USA.

Shirley Fan (S)

Department of Mathematics, Auburn University, Auburn, AL, USA.

Phillippe Gaillard (P)

Department of Mathematics, Auburn University, Auburn, AL, USA.

Elizabeth A Lipke (EA)

Department of Chemical Engineering, Auburn University, Auburn, AL, USA.

Anne A Wooldridge (AA)

Department of Clinical Sciences, Auburn University, Auburn, AL, USA. aaw0002@auburn.edu.

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