Recombinant high‑mobility group box 1 induces cardiomyocyte hypertrophy by regulating the 14‑3‑3η, PI3K and nuclear factor of activated T cells signaling pathways
Autor: | Yan Li, Fei-Fei Su, Jianwei Tian, Jian Zhang, Miaoqian Shi |
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Rok vydání: | 2021 |
Předmět: |
Cancer Research
cardiomyocyte Cardiomegaly high-mobility group box 1 HMGB1 Biochemistry Muscle hypertrophy Wortmannin Mice Phosphatidylinositol 3-Kinases chemistry.chemical_compound Atrial natriuretic peptide Western blot Genetics medicine Animals Myocytes Cardiac HMGB1 Protein Molecular Biology Protein kinase B 14-3-3 PI3K/AKT/mTOR pathway NFATC Transcription Factors biology medicine.diagnostic_test Chemistry Articles Recombinant Proteins Cell biology 14-3-3 Proteins Oncology biology.protein Molecular Medicine Female Signal transduction hypertrophy Proto-Oncogene Proteins c-akt Signal Transduction |
Zdroj: | Molecular Medicine Reports |
ISSN: | 1791-3004 1791-2997 |
DOI: | 10.3892/mmr.2021.11853 |
Popis: | High‑mobility group box 1 (HMGB1) is released by necrotic cells and serves an important role in cardiovascular pathology. However, the effects of HMGB1 in cardiomyocyte hypertrophy remain unclear. Therefore, the aim of the present study was to investigate the potential role of HMGB1 in cardiomyocyte hypertrophy and the underlying mechanisms of its action. Neonatal mouse cardiomyocytes (NMCs) were co‑cultured with recombinant HMGB1 (rHMGB1). Wortmannin was used to inhibit PI3K activity in cardiomyocytes. Subsequently, atrial natriuretic peptide (ANP), 14‑3‑3 and phosphorylated‑Akt (p‑Akt) protein levels were detected using western blot analysis. In addition, nuclear factor of activated T cells 3 (NFAT3) protein levels were measured by western blot analysis and observed in NMCs under a confocal microscope. The results revealed that rHMGB1 increased ANP and p‑Akt, and decreased 14‑3‑3η protein levels. Furthermore, wortmannin abrogated the effects of rHMGB1 on ANP, 14‑3‑3η and p‑Akt protein levels. In addition, rHMGB1 induced nuclear translocation of NFAT3, which was also inhibited by wortmannin pretreatment. The results of this study suggest that rHMGB1 induces cardiac hypertrophy by regulating the 14‑3‑3η/PI3K/Akt/NFAT3 signaling pathway. |
Databáze: | OpenAIRE |
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