Role of Exosomes Derived from miR-133b Modified MSCs in an Experimental Rat Model of Intracerebral Hemorrhage
Autor: | Tiejun Zhang, Chengyuan Ji, Xiang Li, Qing Sun, Gang Chen, Xiyang Yao, Haitao Shen, Haiying Li |
---|---|
Rok vydání: | 2018 |
Předmět: |
Male
0301 basic medicine RHOA Central nervous system Apoptosis Biology Exosomes CREB Exosome Neuroprotection Rats Sprague-Dawley 03 medical and health sciences Cellular and Molecular Neuroscience 0302 clinical medicine Western blot medicine Animals Cyclic AMP Response Element-Binding Protein Cerebral Hemorrhage Mitogen-Activated Protein Kinase 1 Mitogen-Activated Protein Kinase 3 medicine.diagnostic_test Mesenchymal stem cell Mesenchymal Stem Cells General Medicine Microvesicles Rats MicroRNAs 030104 developmental biology medicine.anatomical_structure Cancer research biology.protein 030217 neurology & neurosurgery |
Zdroj: | Journal of Molecular Neuroscience. 64:421-430 |
ISSN: | 1559-1166 0895-8696 |
DOI: | 10.1007/s12031-018-1041-2 |
Popis: | Intracerebral hemorrhage (ICH) has poor outcomes due to high mortality and morbidity, but until now, the effective treatments remain limited. MicroRNAs (miRNAs) are vital regulators of gene expression and demonstrated to be linked to the pathogenesis of various central nervous system (CNS) diseases. Exosomes are considered as cell-to-cell communication vectors and secreted largely by mesenchymal stromal cells (MSCs). The present study investigated the role of miR-133b delivered by exosomes secreted from MSCs to brain tissues in rats after ICH. An autologous arterial blood ICH model in adult male Sprague-Dawley (SD) rats was used in this study. At 72 h after transfection with miR-133b mimics in MSCs, miR-133b-modified MSC-derived exosomes were collected from medium of MSCs and then injected to rats via tail vein. The levels of miR-133b in secreted exosomes and brain tissues of rats in various groups and the levels of RhoA, phosphorylations of extracellular signal regulating kinase (ERK1/2), and cAMP response element-binding protein (CREB) were detected by real-time PCR and western blot analysis, respectively. The effects of miR-133b on neuronal apoptosis and degeneration were respectively evaluated by TUNEL and fluoro-jade B staining. The miR-133b levels were reduced in brain tissues of rats at 24 h and peaked at 72 h after ICH. At 24 h after miR-133b-modified exosome administration, the level of miR-133b was significantly increased, while the apoptotic and neurodegenerative neurons were obviously reduced in brain tissues after ICH. The results of western blot analysis showed that miR-133b modified exosomes treatment remarkably suppressed RhoA expression and activated ERK1/2/CREB in brain tissues after ICH. Collectively, our investigation suggested that exosomes derived from miR-133b modified MSCs exhibited neuroprotective role for anti-apoptotic effect of miR-133b mediating RhoA and ERK1/2/CREB in rats after ICH. |
Databáze: | OpenAIRE |
Externí odkaz: |