Autophagy mediates the secretion of macrophage migration inhibitory factor from cardiomyocytes upon serum-starvation
Autor: | Xiangning Deng, Youyi Zhang, Han Xiao, Wei Gao, Juan Gao, Xinyu Wang, Jimin Wu |
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Rok vydání: | 2019 |
Předmět: |
Male
0301 basic medicine Bodily Secretions animal diseases medicine.medical_treatment Autophagy-Related Protein 5 Rats Sprague-Dawley chemistry.chemical_compound 0302 clinical medicine Myocytes Cardiac Creatine Kinase General Environmental Science Aged 80 and over Middle Aged respiratory system Troponin Cytokine 030220 oncology & carcinogenesis General Agricultural and Biological Sciences Signal Transduction Adult medicine.medical_specialty Adolescent ATG5 Ischemia Myocardial Reperfusion Injury chemical and pharmacologic phenomena General Biochemistry Genetics and Molecular Biology 03 medical and health sciences Internal medicine Lactate dehydrogenase Autophagy otorhinolaryngologic diseases medicine Animals Humans Secretion Acute Coronary Syndrome Macrophage Migration-Inhibitory Factors Cell damage Aged L-Lactate Dehydrogenase business.industry Fibroblasts medicine.disease biological factors Rats 030104 developmental biology Endocrinology chemistry Macrophage migration inhibitory factor business Biomarkers |
Zdroj: | Science China Life Sciences. 62:1038-1046 |
ISSN: | 1869-1889 1674-7305 |
DOI: | 10.1007/s11427-019-9567-1 |
Popis: | Macrophage migration inhibitory factor (MIF) is an inflammatory cytokine. It is elevated early in the blood of acute myocardial infarction patients. However, it is unclear whether and how MIF is released. This study investigated the cellular source and mechanism of MIF release from hearts. An ischemia-mimic treatment induced the secretion of MIF from neonatal rat cardiomyocytes but not from fibroblasts. The treatment did not cause significant leakage of lactate dehydrogenase, suggesting that ischemia induced the MIF secretion without causing severe cell damage. Plasma samples from patients with acute chest pain at the emergency department were collected for the detection of MIF. MIF levels in patients with acute coronary syndrome (ACS) increased early, when cardiac injury markers were not yet elevated, suggesting that ischemia can induce MIF secretion before the occurrence of severe myocardial damage. Serum-starvation caused MIF secretion from rat cardiomyocytes and Langendorff-perfused rat hearts. The secretion was suppressed by the inhibition of autophagy by inhibitors or by silencing of Atg5. In conclusion, serum-starvation induces the secretion of MIF from cardiomyocytes via autophagy dependent pathway. Clarifying the mechanism of MIF secretion will be helpful for its application in the early diagnosis and treatment of ACS. |
Databáze: | OpenAIRE |
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