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Review
. 2010 May;14(5):1044-55.
doi: 10.1111/j.1582-4934.2010.01046.x. Epub 2010 Feb 27.

Injectable cardiac tissue engineering for the treatment of myocardial infarction

Affiliations
Review

Injectable cardiac tissue engineering for the treatment of myocardial infarction

Haibin Wang et al. J Cell Mol Med. 2010 May.

Abstract

Future perspectives Heart disease is a leading cause of morbidity and mortality worldwide. Myocardial infarction leads to permanent loss of cardiac tissue and ultimately heart failure. However, current therapies could only stall the progression of the disease. Thus, new therapies are needed to regenerate damaged hearts to overcome poor prognosis of patients with heart failure. The shortage of heart donors is also a factor for innovating new therapies. Although the cardiac performance by cell-based therapy has improved, unsatisfactory cell retention and transplant survival still plague this technique. Because biomaterials can improve the cell retention, survival and differentiation, cardiac tissue engineering is now being explored as an approach to support cell-based therapies and enhance their efficacy for cardiac disease. In the last decade, cardiac tissue engineering has made considerable progress. Among different kinds of approaches in the cardiac tissue engineering, the approach of injectable cardiac tissue engineering is more minimally invasive than that of in vitro engineered tissue or epicardial patch implantation. It is therefore clinically appealing. In this review, we strive to describe the major progress in the filed of injectable cardiac tissue engineering, including seeding cell sources, biomaterials and novel findings in preclinical studies and clinical applications. The remaining problems will also be discussed.

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Figures

Fig 1
Fig 1
Schematic diagram illustrating the strategies of injectable cardiac tissue engineering for the treatment of myocardial infarction. The injectable biomaterials can deliver cells directly into the infarcted wall. They can also be utilized in acellular approaches to support the LV wall and avoid the negative remodelling after an MI, or for the controlled delivery of therapeutic genes and proteins to ischaemic myocardium.

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