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LIN28 Expression in Rat Spinal Cord After Injury
Authors:Ying Yue  Dongmei Zhang  Shengyang Jiang  Aihong Li  Aisong Guo  Xinming Wu  Xiaopeng Xia  Hongbing Cheng  Tao Tao  Xingxing Gu
Institution:1. The Jiangsu Key Laboratory of Neuroregeneration, Nantong University, Nantong, 226001, People’s Republic of China
2. Department of Pathogen Biology, Medical School, Nantong University, Nantong, 226001, People’s Republic of China
3. Basic Medial Research Center, Medical School, Nantong University, Nantong, 226001, People’s Republic of China
4. Department of Neurology, Affiliated Hospital of Nantong University, Nantong, 226001, People’s Republic of China
5. Department of Orthopaedics, Traditional Chinese Medical Hospital of Nantong City, Nantong, 226001, People’s Republic of China
6. Department of Chemistry and Institutes of Biomedical Sciences, Fudan University, Shanghai, 200433, People’s Republic of China
Abstract:LIN28, an RNA-binding protein, is known to be involved in the regulation of many cellular processes, such as embryonic stem cell proliferation, cell fate succession, developmental timing, and oncogenesis. However, its expression and function in central nervous system still unclear. In this study, we performed an acute spinal cord contusion injury (SCI) model in adult rats and investigated the dynamic changes of LIN28 expression in spinal cord. Western blot and immunohistochemistry analysis revealed that LIN28 was present in normal spinal cord. It gradually increased, reached a peak at 3 day, and then nearly declined to the basal level at 14 days after SCI. Double immunofluorescence staining showed that LIN28 immunoreactivity was found in neurons, astrocytes and a handful of microglia. Interestingly, LIN28 expression was increased predominantly in astrocytes but not in neurons. Moreover, the colocalization of LIN28 and proliferating cell nuclear antigen was detected after injury. Western blot showed that LIN28 participated in lipopolysaccharide (LPS) induced astrocytes inflammatory responses by NF-κB signaling pathway. These results suggested that LIN28 may be involved in the pathologic process of SCI, and further research is needed to have a good understanding of its function and mechanism.
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