The Modulation of Neurotrophin and Epigenetic Regulators: Implication for Astrocyte Proliferation and Neuronal Cell Apoptosis After Spinal Cord Injury
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Objective To investigate alterations in the expression of the main regulators of neuronal survival and death related to astrocytes and neuronal cells in the brain in a mouse model of spinal cord injury (SCI). Methods Eight-week-old male imprinting control region mice (n=36; 30–35 g) were used in this study and randomly assigned to two groups: the naïve control group (n=18) and SCI group (n=18). The mice in both groups were randomly allocated to the following three time points: 3 days, 1 week, and 2 weeks (n=6 each). The expression levels of regulators such as brain-derived neurotrophic factor (BDNF), glial cell line-derived neurotrophic factor (GDNF), nerve growth factor (NGF), histone deacetylase 1 (HDAC1), and methyl-CpG-binding protein 2 (MeCP 2) in the brain were evaluated following thoracic contusive SCI. In addition, the number of neuronal cells in the motor cortex (M1 and M2 areas) and the number of astrocytes in the hippocampus were determined by immunohistochemistry. Results BDNF expression was significantly elevated at 2 weeks after injury (p=0.024). The GDNF level was significantly elevated at 3 days (p=0.042). The expression of HDAC1 was significantly elevated at 1 week (p=0.026). Following SCI, compared with the control the number of NeuN-positive cells in the M1 and M2 areas gradually and consistently decreased at 2 weeks after injury. In contrast, the number of astrocytes was significantly increased at 1 week (p=0.029).Conclusion These results demonstrate that the upregulation of BDNF, GDNF and HDAC1 might play on important role in brain reorganization after SCI.
Abstract
Objective To investigate alterations in the expression of the main regulators of neuronal survival and death related to astrocytes and neuronal cells in the brain in a mouse model of spinal cord injury (SCI). Methods Eight-week-old male imprinting control region mice (n=36; 30–35 g) were used in this study and randomly assigned to two groups: the naïve control group (n=18) and SCI group (n=18). The mice in both groups were randomly allocated to the following three time points: 3 days, 1 week, and 2 weeks (n=6 each). The expression levels of regulators such as brain-derived neurotrophic factor (BDNF), glial cell line-derived neurotrophic factor (GDNF), nerve growth factor (NGF), histone deacetylase 1 (HDAC1), and methyl-CpG-binding protein 2 (MeCP 2) in the brain were evaluated following thoracic contusive SCI. In addition, the number of neuronal cells in the motor cortex (M1 and M2 areas) and the number of astrocytes in the hippocampus were determined by immunohistochemistry. Results BDNF expression was significantly elevated at 2 weeks after injury (p=0.024). The GDNF level was significantly elevated at 3 days (p=0.042). The expression of HDAC1 was significantly elevated at 1 week (p=0.026). Following SCI, compared with the control the number of NeuN-positive cells in the M1 and M2 areas gradually and consistently decreased at 2 weeks after injury. In contrast, the number of astrocytes was significantly increased at 1 week (p=0.029).Conclusion These results demonstrate that the upregulation of BDNF, GDNF and HDAC1 might play on important role in brain reorganization after SCI.
참고문헌 (24)
- Bregman BS, "Infant lesion effect. II:Sparing and recovery of function after spinal cord damage in newborn and adult cats", Brain Res, 285, pp.119~135 (1983)
- 유송희, "The Neuroprotective Effect of Treatment of Valproic Acid in Acute Spinal Cord Injury", 대한신경외과학회지, 51(4), pp.191~198 (2012), 대한신경외과학회[DOI]
- Burns SP, "Recovery of ambulation in motor-incomplete tetraplegia", Arch Phys Med Rehabil, 78, pp.1169~1172 (1997)
- Raineteau O, "Plasticity of motor systems after incomplete spinal cord injury", Nat Rev Neurosci, 2, pp.263~273 (2001)
- Jain N, "Deactivation and reactivation of somatosensory cortex after dorsal spinal cord injury", Nature, 386, pp.495~498 (1997)
- Florence SL, "Large-scale sprouting of cortical connections after peripheral injury in adult macaque monkeys", Science, 282, pp.1117~1121 (1998)
- Bruehlmeier M, "How does the human brain deal with a spinal cord injury?", Eur J Neurosci, 10, pp.3918~3922 (1998)
- Curt A, "Differential effect of spinal cord injury and functional impairment on human brain activation", J Neurotrauma, 19, pp.43~51 (2002)
- Green JB, "Cortical sensorimotor reorganization after spinal cord injury: an electroencephalographic study", Neurology, 50, pp.1115~1121 (1998)
- McKinley PA, "Age-dependent capacity for somatosensory cortex reorganization in chronic spinal cats", Brain Res, 428, pp.136~139 (1987)
- Boutillier AL, "Selective E2Fdependent gene transcription is controlled by histone deacetylase activity during neuronal apoptosis", J Neurochem, 84, pp.814~828 (2003)
- Legube G, "Regulating histone acetyltransferases and deacetylases", EMBO Rep, 4, pp.944~947 (2003)
- Kumar A, "Neuroinflammation after traumatic brain injury: opportunities for therapeutic intervention", Brain Behav Immun, 26, pp.1191~1201 (2012)
- Wu J, "Isolated spinal cord contusion in rats induces chronic brain neuroinflammation, neurodegeneration, and cognitive impairment. Involvement of cell cycle activation", Cell Cycle, 13, pp.2446~2458 (2014)
- Kim BG, "Remodeling of synaptic structures in the motor cortex following spinal cord injury", Exp Neurol, 198, pp.401~415 (2006)
- Lee R, "Regulation of cell survival by secreted proneurotrophins", Science, 294, pp.1945~1948 (2001)
- Seidah NG, "Proprotein and prohormone convertases: a family of subtilases generating diverse bioactive polypeptides", Brain Res, 848, pp.45~62 (1999)
- Seidah NG, "Cellular processing of the neurotrophin precursors of NT3 and BDNF by the mammalian proprotein convertases", FEBS Lett, 379, pp.247~250 (1996)
- Ying SW, "Brain-derived neurotrophic factor induces long-term potentiation in intact adult hippocampus:requirement for ERK activation coupled to CREB and upregulation of Arc synthesis", J Neurosci, 22, pp.1532~1540 (2002)
- Endo T, "Cortical sensory map rearrangement after spinal cord injury: fMRI responses linked to Nogo signalling", Brain, 130(Pt 11), pp.2951~2961 (2007)
- Buss A, "Gradual loss of myelin and formation of an astrocytic scar during Wallerian degeneration in the human spinal cord", Brain, 127(Pt 1), pp.34~44 (2004)
- Wrigley PJ, "Anatomical changes in human motor cortex and motor pathways following complete thoracic spinal cord injury", Cereb Cortex, 19, pp.224~232 (2009)
- Mowla SJ, "Differential sorting of nerve growth factor and brain-derived neurotrophic factor in hippocampal neurons", J Neurosci, 19, pp.2069~2080 (1999)
- Sydekum E, "Rapid functional reorganization of the forelimb cortical representation after thoracic spinal cord injury in adult rats", Neuroimage, 87, pp.72~79 (2014)
