Abstract

BackgroundLittle is known about the differences among adult and foetal equine mesenchymal stem cells (MSCs), and no data exist about their comparative ultrastructural morphology. The aim of this study was to describe and compare characteristics, immune properties, and ultrastructural morphology of equine adult (bone marrow: BM, and adipose tissue: AT) and foetal adnexa derived (umbilical cord blood: UCB, and Wharton’s jelly: WJ) MSCs.ResultsNo differences were observed in proliferation during the first 3 passages. While migration ability was similar among cells, foetal MSCs showed a higher adhesion ability, forming smaller spheroids after hanging drop culture (P < 0.05). All MSCs differentiated toward adipogenic, chondrogenic and osteogenic lineages, only tenogenic differentiation was less evident for WJ-MSCs. Data obtained by PCR confirmed MHC1 expression and lack of MHC2 expression in all four cell types. Foetal adnexa MSCs were positive for genes specific for anti-inflammatory and angiogenic factors (IL6, IL8, ILβ1) and WJ-MSCs were the only positive for OCT4 pluripotency gene. At immunofluorescence all cells expressed typical mesenchymal markers (α-SMA, N-cadherin), except for BM-MSCs, which did not express N-cadherin. By transmission electron microscopy, it was observed that WJ-MSCs had a higher (P < 0.05) number of microvesicles compared to adult MSCs, and UCB-MSCs showed more microvesicles than BM-MSCs (P < 0.05). AT-MSCs had a lower number of mitochondria than WJ-MSCs (P < 0.05), and mitochondrial area was higher for WJ-MSCs compared to UCB and AT-MSCs (P < 0.05).ConclusionsResults demonstrate that MSCs from adult and foetal tissues have different characteristics, and foetal MSCs, particularly WJ derived ones, seem to have some charactestics that warrant further investigation into potential advantages for clinical application.

Highlights

  • Little is known about the differences among adult and foetal equine mesenchymal stem cells (MSCs), and no data exist about their comparative ultrastructural morphology

  • In vivo application for treatment of horse tendon and ligament injuries of bone marrow (BM) and amniotic membrane MSCs confirmed the advantage to administer allogeneic amniotic membrane MSCs when needed, before any ultrasonographic change occurs within the injured tendon and ligament, and the lower re-injury rate observed after amniotic MSCs treatment let suppose that their implantation is more efficacious compared to BM-MSCs implantation [9]

  • Due to the large variation observed for ATMSCs, average percentage of migration, observed by scratch test, was similar (P > 0.05) between cell types (WJ-MSCs 43.0 ± 7.7%, umbilical cord blood (UCB)-MSCs 28.4 ± 5.0%, BMMSCs: 25.0 ± 10.2%, adipose tissue (AT)-MSCs 24.5 ± 21.4%) when analysed by one-way ANOVA

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Summary

Introduction

Little is known about the differences among adult and foetal equine mesenchymal stem cells (MSCs), and no data exist about their comparative ultrastructural morphology. The aim of this study was to describe and compare characteristics, immune properties, and ultrastructural morphology of equine adult (bone marrow: BM, and adipose tissue: AT) and foetal adnexa derived (umbilical cord blood: UCB, and Wharton’s jelly: WJ) MSCs. Mesenchymal stem cells (MSCs), known as multipotent stromal cells or mesenchymal progenitor cells, are of increasing interest in the regenerative medicine field. Despite the common characterization and clinical applicability potential for all the different sources of MSCs, In the horse, MSCs from bone marrow (BM) possessed the highest in vitro osteogenic potential compared to adipose tissue (AT) and umbilical cord blood (UCB) and. In vivo application for treatment of horse tendon and ligament injuries of BM and amniotic membrane MSCs confirmed the advantage to administer allogeneic amniotic membrane MSCs when needed, before any ultrasonographic change occurs within the injured tendon and ligament, and the lower re-injury rate observed after amniotic MSCs treatment let suppose that their implantation is more efficacious compared to BM-MSCs implantation [9]

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