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Updated: Jun 27, 2026

Intramyocardial Cell Delivery: Observations in Murine Hearts
Published on: January 24, 2014
Comparison of different adult stem cell types for treatment of myocardial ischemia
Koen E A van der Bogt1, Ahmad Y Sheikh, Sonja Schrepfer
1Laboratory of Cardiothoracic Transplantation, Stanford University School of Medicine, Stanford, CA 94305-5324, USA.
Background:
A comparative analysis of the efficacy of different cell candidates for the treatment of heart disease remains to be described. This study is designed to evaluate the therapeutic efficacy of 4 cell types in a murine model of myocardial infarction.
Methods And Results:
Bone marrow mononuclear cells (MN), mesenchymal stem cells (MSC), skeletal myoblasts (SkMb), and fibroblasts (Fibro) expressing firefly luciferase (Fluc) and green fluorescence protein (GFP) were characterized by flow cytometry, bioluminescence imaging (BLI), and luminometry. Female FVB mice (n=70) underwent LAD ligation and intramyocardially received one cell type (5x10(5)) or PBS. Cell survival was measured by BLI and by TaqMan PCR. Cardiac function was assessed by echocardiography and invasive hemodynamic measurements. Fluc expression correlated with cell number in all groups (r(2)>0.93). In vivo BLI revealed acute donor cell death of MSC, SkMb, and Fibro within 3 weeks after transplantation. By contrast, cardiac signals were still present after 6 weeks in the MN group, as confirmed by TaqMan PCR (P<0.01). Echocardiography showed significant preservation of fractional shortening in the MN group compared to controls (P<0.05). Measurements of left ventricular end-systolic/diastolic volumes revealed that the least amount of ventricular dilatation occurred in the MN group (P<0.05). Histology confirmed the presence of MN, although there was no evidence of transdifferentiation by donor MN into cardiomyocytes.
Conclusions:
This is the first study to show that compared to MSC, SkMB, and Fibro, MN exhibit a more favorable survival pattern, which translates into a more robust preservation of cardiac function.
Insights
Bone marrow mononuclear cells (MN) showed better survival and preserved cardiac function in a myocardial infarction model compared to mesenchymal stem cells (MSC), skeletal myoblasts (SkMb), and fibroblasts (Fibro). This finding highlights MN as a promising cell therapy for heart disease.
Area of Science:
- Regenerative Medicine
- Cardiovascular Research
- Cell Therapy
Background:
- The efficacy of various cell types for treating heart disease requires comparative analysis.
- Current research lacks a clear understanding of optimal cell candidates for myocardial infarction therapy.
Purpose of the Study:
- To evaluate and compare the therapeutic efficacy of four distinct cell types in a murine model of myocardial infarction.
- To assess cell survival, cardiac function, and ventricular remodeling following cell transplantation.
Main Methods:
- Four cell types (bone marrow mononuclear cells, mesenchymal stem cells, skeletal myoblasts, fibroblasts) were characterized and transplanted into mice post-myocardial infarction.
- Cell survival was monitored using bioluminescence imaging and TaqMan PCR.
- Cardiac function was assessed via echocardiography and hemodynamic measurements.
Main Results:
- Bone marrow mononuclear cells (MN) demonstrated significantly longer survival compared to mesenchymal stem cells (MSC), skeletal myoblasts (SkMb), and fibroblasts (Fibro).
- MN transplantation led to significant preservation of fractional shortening and reduced ventricular dilatation.
- While MN were present, no evidence of transdifferentiation into cardiomyocytes was observed.
Conclusions:
- Bone marrow mononuclear cells (MN) exhibit superior survival rates compared to MSC, SkMb, and Fibro in a myocardial infarction model.
- The enhanced survival of MN translates to more effective preservation of cardiac function.
- MN represent a promising cell candidate for myocardial infarction treatment due to their favorable survival and functional outcomes.
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