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temporal differences in microrna expression patterns in astrocytes and neurons after ischemic injury时间微rna表达模式的差异在缺血性损伤后星形胶质细胞和神经元.pdfVIP

temporal differences in microrna expression patterns in astrocytes and neurons after ischemic injury时间微rna表达模式的差异在缺血性损伤后星形胶质细胞和神经元.pdf

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temporal differences in microrna expression patterns in astrocytes and neurons after ischemic injury时间微rna表达模式的差异在缺血性损伤后星形胶质细胞和神经元

Temporal Differences in MicroRNA Expression Patterns in Astrocytes and Neurons after Ischemic Injury Mateo Ziu, Lauren Fletcher, Shushan Rana, David F. Jimenez, Murat Digicaylioglu* Department of Neurosurgery, University of Texas Health Science Center at San Antonio, San Antonio, Texas, United States of America Abstract MicroRNAs (miRNAs) are small, non-protein-coding RNA molecules that modulate gene translation. Their expression is altered in many central nervous system (CNS) injuries suggesting a role in the cellular response to stress. Current studies in brain tissue have not yet described the cell-specific temporal miRNA expression patterns following ischemic injury. In this study, we analyzed the expression alterations of a set of miRNAs in neurons and astrocytes subjected to 60 minutes of ischemia and collected at different time-points following this injury. To mimic ischemic conditions and reperfusion in vitro, cortical primary neuronal and astrocytic cultures prepared from fetal rats were first placed in oxygen and glucose deprived (OGD) medium for 60 minutes, followed by their transfer into normoxic pre-conditioned medium. Total RNA was extracted at different time-points after the termination of the ischemic insult and the expression levels of miRNAs were measured. In neurons exposed to OGD, expression of miR-29b was upregulated 2-fold within 6 h and up to 4-fold at 24 h post-OGD, whereas induction of miR-21 was upregulated 2-fold after 24 h when compared to expression in neurons under normoxic conditions. In contrast, in astrocytes, miR-29b and miR-21 were upregulated only after 12 h. MiR-30b, 107, and 137 showed expression alteration in astrocytes, but not in neurons. Furthermore, we show that expression of miR-29b was significantly decreased in neurons exposed to Insulin-Like Growth Factor I (IGF-I), a well documented neuroprot

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