Abstract

Point-of-care kits to concentrate bone marrow (BM)-derived mesenchymal stem cells (MSCs) are used clinically in horses. A maximal number of MSCs per milliliter of marrow aspirated might be desired prior to use of a point-of-care system to concentrate MSCs. Our objective was to test a method to increase the number of MSCs per milliliter of marrow collected. We collected two BM aspirates using two different collection techniques from 12 horses. The first collection technique was to aspirate BM from a single site without advancement of the biopsy needle. The second collection technique was to aspirate marrow from multiple sites within the same sternal puncture by advancing the needle 5 mm three times for BM aspiration from four sites. Numbers of MSCs in collected BM were assessed by total nucleated cell count of BM after aspiration, total colony-forming unit-fibroblast (CFU-F) assay, and total MSC number at each culture passage. The BM aspiration technique of four needle advancements during BM aspiration resulted in higher initial nucleated cell counts, more CFU-Fs, and more MSCs at the first passage. There were no differences in the number of MSCs at later passages. Multiple advancements of the BM needle during BM aspiration resulted in increased MSC concentration at the time of BM collection. If a point-of-care kit is used to concentrate MSCs, multiple advancements may result in higher MSC numbers in the BM concentrate after preparation by the point-of-care kit. For culture expanded MSCs beyond the first cell passage, the difference is of questionable clinical relevance.

Highlights

  • Grafting of autologous bone marrow (BM)-derived cells, as raw BM [1], concentrated BM [2], or BM-derived culture expanded mesenchymal stem cells (MSCs) [3] is used in the horse as a regenerative therapy

  • Our objective was to determine whether multiple advancements (MS) within the same sternal puncture would result in a greater number of MSCs in a 56-ml BM aspirate compared to collection of 56 ml BM from a single site (SS)

  • We found a significantly higher number of nucleated cells in the BM aspirate, and after culture a significantly higher number of colony-forming unit-fibroblast (CFU-F) and a significantly higher number of MSCs at the first passage from multiple sites (MS) compared to SS aspirates

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Summary

Introduction

Grafting of autologous bone marrow (BM)-derived cells, as raw BM [1], concentrated BM [2], or BM-derived culture expanded mesenchymal stem cells (MSCs) [3] is used in the horse as a regenerative therapy. One major difference is the timing of therapeutic application Both raw BM and concentrated BM can be used for point-of-care therapy, whereas BM-derived MSCs typically undergo a 2- to 4-week culture period [4] prior to implantation. The ability to increase the Needle Advancement Increases MSC Concentration mononuclear fraction in BMAC compared to BM has been well described in multiple species ranging from an increase of 2.4- to 5-fold in people [6], 7-fold in dogs [7], 3.5-fold in pigs [8], and 5- to 19-fold in the horse [9]. In people with atrophic tibial diaphyseal non-union, treatment success with either BM or BMAC was related to the number of progenitors in the graft [10]

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