Abstract

Background : Equine amnion mesenchymal stem cells (EAMSCs) from amnion isolated after the foal birth represented an alternative source of easy collection of mesenchymal cells used in equine regenerative medicine. Methods : These cells grown as 2D culture in α-MEM medium supplemented with EGF were differentiated in adipogenic, chondrogenic and osteogenic cells. Half a million cells as pellet were left in 15ml tubes with the same differentiation media for 20 days. After the pellets were collected, embedded in paraffin for morphological study. Results : 2D culture showed EAMSCs with an embryonic phenotype (C-kit+, CD105+, Oct-4+) and a differentiation potential in adipogenic, chondrogenic and osteogenic multipotent cells. By a reproducible method of 3D culture, at day 20 the Authors evidenced a formation of small aggregated spheroids gradually gathering. In cross sections the surface of spheroid evidenced flattened cells embedded in a red matrix by Alizarin staining and occasionally a core of calcium precipitation. A network of apoptotic or necrotic cells in a not mineralized matrix was present into the center of nodules. The 3D spheroids appeared larger (mean diameter of 605±53 µm for gathering spheroids and 1486±79 µm for spheroids already gathered) than those from standard monolayer cultures (mean diameter of 200 ± 73 µm). Conclusions : EAMSCs cultured in 3D method preserve their in vitro multipotent differentiation than adherent 2D culture method. These EAMSCs included in extracellular matrix not mineralized at day 20 seem to be a good source of MSCs for tissue repair and regeneration in equine medicine.

Highlights

  • Equine mesenchymal stem cells (EMSCs) were isolated from bone marrow [1,2,3,4], adipose tissue [5], peripheral blood [1] and cord blood [6,7]

  • Equine amnion mesenchymal stem cells (EAMSCs) cultured in 3D method preserve their in vitro multipotent differentiation than adherent 2-D culture method

  • These EAMSCs included in the extracellular matrix not mineralized at day 20 seem to be a good source of MSCs for tissue repair and regeneration in equine medicine

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Summary

Introduction

Equine mesenchymal stem cells (EMSCs) were isolated from bone marrow [1,2,3,4], adipose tissue [5], peripheral blood [1] and cord blood [6,7]. There is an increasing interest in the investigation of adult extra-embryonic tissues such as fetal adnexa (amnion, amniotic fluid and Wharton jelly) [8,9,10] due to easy collection after birth of the foal. Among the equine fetal adnexa, the amnion has been recently studied as an alternative source of mesenchymal cells used in the field of equine regenerative medicine. Equine amnion mesenchymal stem cells (EAMSCs) from amnion isolated after the foal birth represented an alternative source of easy collection of mesenchymal cells used in equine regenerative medicine

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