Abstract

Intracoronary injection of bone marrow mononuclear cells (BMMNC) is an emerging treatment for heart failure. Initial donor cell retention in the heart is the key to the success of this approach, but this process remains insufficiently characterized. Although it is assumed that cell size of injected cells may influence their initial retention, no scientific evidence has been reported. We developed a unique model utilizing an ex-vivo rat heart perfusion system, enabling quantitative assessment of retention of donor cells after intracoronary injection. The initial (5 minutes after intracoronary injection) retention rate of BMMNC was as low as approximately 20% irrespective of donor cell doses injected (1×106, 8×106, 4×107). Quantitative cell-size assessment revealed a positive relationship between the size of BMMNC and retention ratio; larger subpopulations of BMMNC were more preferentially retained compared to smaller ones. Furthermore, a larger cell type—bone marrow-derived mesenchymal stromal cells (median size = 11.5μm versus 7.0μm for BMMNC)—had a markedly increased retention rate (77.5±1.8%). A positive relationship between the cell size and retention ratio was also seen in mesenchymal stromal cells. Flow-cytometric studies showed expression of cell-surface proteins, including integrins and selectin-ligands, was unchanged between pre-injection BMMNC and those exited from the heart, suggesting that biochemical interaction between donor cells and host coronary endothelium is not critical for BMMNC retention. Histological analyses showed that retained BMMNC and mesenchymal stromal cells were entrapped in the coronary vasculature and did not extravasate by 60 minutes after transplantation. Whilst BMMNC did not change coronary flow after intracoronary injection, mesenchymal stromal cells reduced it, suggesting coronary embolism, which was supported by the histological finding of intravascular cell-clump formation. These data indicate that cell-size dependent, passive (mechanical), intravascular entrapment is responsible for the initial donor cell retention after intracoronary injection of BMMNC in the heart having normal vasculatures (at least).

Highlights

  • Transplantation of unfractionated bone marrow mononuclear cells (BMMNC) via intracoronary (IC) injection is a promising approach for the treatment of acute myocardial infarction and chronic heart failure [1,2,3,4,5,6]

  • Using our original rat model based on Langendorff ex-vivo heart perfusion, donor cell loss was quantified minute-by-minute after IC injection of rat BMMNC (1×106, 8×106 or 40×106 cells injected)

  • The BMMNC retention rate at 5 minutes was poor (~20%) after IC injection into the normal heart, and this proportion was consistent between three different BMMNC doses

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Summary

Introduction

Transplantation of unfractionated bone marrow mononuclear cells (BMMNC) via intracoronary (IC) injection is a promising approach for the treatment of acute myocardial infarction and chronic heart failure [1,2,3,4,5,6]. Engraftment of donor cells after IC injection is the consequence of a number of donor cell behaviors, including initial retention, trans-endothelial migration into myocardial interstitium (or integration into vascular walls) and survival with/without differentiation. Among these processes, initial retention has been suggested to be the major determinant of successful engraftment of transplanted cells via IC injection [15,16]. Our understanding of the mechanism responsible for the initial donor cell retention remains insufficient

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