Why the study?
Nanofibrous electrospun scaffolds rarely permit cell infiltration for 3D cardiac tissue constructs, prompting the development of novel bimodal electrospun scaffolds.
Does a Col/PLGA bimodal cardiac patch laden with BMSCs improve cardiac function and attenuate remodeling in a rabbit myocardial infarction model?
Does a Col/PLGA bimodal cardiac patch laden with BMSCs improve cardiac function and attenuate remodeling in a rabbit myocardial infarction model?
p-value: p=<0.05
A Col/PLGA bimodal cardiac patch laden with mesenchymal stem cells significantly improved myocardial contractility and attenuated cardiac remodeling in a preclinical rabbit model of myocardial infarction.
Novel electrospun cardiac patches merit preclinical follow-up; leaves open any clinical role in regeneration.
BACKGROUND: Although the use of cardiac patches is still controversial, cardiac patch has the significance in the field of the tissue engineered cardiac regeneration because it overcomes several shortcomings of intra-myocardial injection by providing a template for cells to form a cohesive sheet. So far, fibrous scaffolds fabricated using electrospinning technique have been increasingly explored for preparation of cardiac patches. One of the problems with the use of electrospinning is that nanofibrous structures hardly allow the infiltration of cells for development of 3D tissue construct. In this respect, we have prepared novel bi-modal electrospun scaffolds as a feasible strategy to address the challenges in cardiac tissue engineering . METHODS: Nano/micro bimodal composite fibrous patch composed of collagen and poly (D, L-lactic-co-glycolic acid) (Col/PLGA) was fabricated using an independent nozzle control multi-electrospinning apparatus, and its feasibility as the stem cell laden cardiac patch was systemically investigated. RESULTS: Nano/micro bimodal distributions of Col/PLGA patches without beaded fibers were obtained in the range of the 4-6% collagen concentration. The poor mechanical properties of collagen and the hydrophobic property of PLGA were improved by co-electrospinning. In vitro experiments using bone marrow-derived mesenchymal stem cells (BMSCs) revealed that Col/PLGA showed improved cyto-compatibility and proliferation capacity compared to PLGA, and their extent increased with increase in collagen content. The results of tracing nanoparticle-labeled as well as GFP transfected BMSCs strongly support that Col/PLGA possesses the long-term stem cells retention capability, thereby allowing stem cells to directly function as myocardial and vascular endothelial cells or to secrete the recovery factors, which in turn leads to improved heart function proved by histological and echocardiographic findings. CONCLUSION: Col/PLGA bimodal cardiac patch could significantly attenuate cardiac remodeling and fully recover the cardiac function, as a consequence of their potent long term stem cell engraftment capability.
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Wee et al. (2022) studied Myocardial infarction (n=15). Col/PLGA bimodal fibrous patch laden with BMSCs vs. No treatment (MI group) was evaluated on Left ventricular fractional shortening (LVFS) and ejection fraction (LVEF) (p=<0.05).
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