Generation of induced pluripotent stem cells using skin fibroblasts from patients with myocardial infarction under feeder-free conditions

Abstract

Abstract. Myocardial infarction (MI) is an increasing medical problem; however, its pathogenesis has yet to be elucidated and more effective treatment strategies are required. Induced pluripotent stem cells (iPSCs) were recently successfully generated using human somatic cells transfected with four transcription factors. The present study aimed to generate iPSCs from cells from patients with myocardial infarction. Six patients who had been diagnosed with myocardial infarction were enrolled in this study. The fibroblast cells from the biopsied skin were reprogrammed using octamer-binding transcription factor 4 (Oct-4), SRY-related HMG-box gene 2 (Sox-2), Kruppel-like factor 4 (Klf-4) and cellular myelocytomatosis oncogene (c-Myc) transcription factors. The generated cells were identified by karyotyping, in vitro and in vivo differentiation ability and staining for specific markers. These human MI-iPSCs expressed pluripotent genes and cell surface markers, and exhibited normal proliferation. The iPSCs also showed in vivo and in vitro differentiation ability, as indicated by teratoma and embryoid body formation, respectively. Moreover, the iPSCs differentiated into cardiomyocytes and neuronal cells. In conclusion, human iPSCs were successfully generated from skin fibroblasts from patients with MI under feeder-independent conditions, which increases their potential suitability for clinical applications. These results may encourage further study of MI pathogenesis and facilitate the development of safe downstream clinical applications of iPSC-based cell therapies.

Inhibition of MiR-92a May Protect Endothelial Cells After Acute Myocardial Infarction in Rats: Role of KLF2/4

“…Published studies mainly focus on the association between MI and cardiomyocyte death, including apoptosis and necrosis [ 32 ]. Existing experiments in vitro revealed that miR-92a has effects on some cardiac diseases, such as endothelial inflammatory, atherosclerosis, and ischemia-reperfusion injury [ 25 , 33 ].…”

LncRNA MHRT Promotes Cardiac Fibrosis via miR-3185 Pathway Following Myocardial Infarction

“…7) If the ischemia or fibrosis reaction is continuously induced, the extracellular matrix will be excessively deposited, resulting in fibrous scar formation, which will further change the shape and structure of the heart and reduce the compliance of the heart. 8,9) Moreover, excessive accumulation of extracellular matrix easily induces arrhythmias and leads to permanent arrhythmia. 10) Therefore, preventing excessive myocardial fibrosis, late reactive fibrosis of MI, is an important research direction for interventional treatment of acute MI disease.…”