Regenerative strategies for the consequences of myocardial infarction: Chronological indication and upcoming visions

Biomed Pharmacother. 2022 Feb:146:112584. doi: 10.1016/j.biopha.2021.112584. Epub 2021 Dec 27.

Abstract

Heart muscle injury and an elevated troponin level signify myocardial infarction (MI), which may result in defective and uncoordinated segments, reduced cardiac output, and ultimately, death. Physicians apply thrombolytic therapy, coronary artery bypass graft (CABG) surgery, or percutaneous coronary intervention (PCI) to recanalize and restore blood flow to the coronary arteries, albeit they were not convincingly able to solve the heart problems. Thus, researchers aim to introduce novel substitutional therapies for regenerating and functionalizing damaged cardiac tissue based on engineering concepts. Cell-based engineering approaches, utilizing biomaterials, gene, drug, growth factor delivery systems, and tissue engineering are the most leading studies in the field of heart regeneration. Also, understanding the primary cause of MI and thus selecting the most efficient treatment method can be enhanced by preparing microdevices so-called heart-on-a-chip. In this regard, microfluidic approaches can be used as diagnostic platforms or drug screening in cardiac disease treatment. Additionally, bioprinting technique with whole organ 3D printing of human heart with major vessels, cardiomyocytes and endothelial cells can be an ideal goal for cardiac tissue engineering and remarkable achievement in near future. Consequently, this review discusses the different aspects, advancements, and challenges of the mentioned methods with presenting the advantages and disadvantages, chronological indications, and application prospects of various novel therapeutic approaches.

Keywords: Cardiac cell engineering; Cardiac drug delivery systems; Myocardial infarction (MI); Tissue engineering.

Publication types

  • Review

MeSH terms

  • Biocompatible Materials / metabolism
  • Cell Engineering / methods
  • Drug Delivery Systems / methods
  • Extracellular Vesicles / metabolism
  • Fibroblasts / metabolism
  • Genetic Therapy / methods
  • Heart Failure / physiopathology
  • Humans
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Mesenchymal Stem Cells / metabolism
  • Microfluidics / methods
  • Myoblasts, Skeletal / metabolism
  • Myocardial Infarction / physiopathology*
  • Myocardial Ischemia / physiopathology
  • Regeneration / physiology*
  • Stem Cells / metabolism
  • Tissue Engineering / methods

Substances

  • Biocompatible Materials
  • Intercellular Signaling Peptides and Proteins