Changes in the Neurogenesis and Axonal Sprouting in the Organotypic Hippocampal Slice Culture by Aβ25–35 Treatment
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Induction of neurogenesis can occur in the hippocampus in response to various pathological conditions, such as Alzheimer’s disease. The aim of this study was to investigate the changes that occur in endogenous neural stem cells in response to amyloid beta (Aβ)25-35-induced neuronal cell damage in organotypic hippocampal slice cultures. Cresyl violet staining and Fluoro-Jade B staining were used to detect neuronal cell damage and changes of mossy fiber terminals were observed by Timm’s staining. The immunofl uorescence staining was used to detect the newly generated cells in the subgranular zone (SGZ) of the dentate gyrus with specific marker, 5-bromo-2′-deoxyuridine (BrdU), Ki-67, Nestin, and doublecortin (DCX). In compared to control slices, neuronal cell damage was observed and the mossy fi bers were expanded to CA3 area by treatment with Aβ25-35. Ki-67/Nestin- and BrdU/DCX-positive cells were detected in the SGZ. In conclusion, these results demonstrate that Aβ-induced neuronal damage results in an increase in endogenous neural stem cells in rat hippocampal slice cultures not only for gliosis but also for neurogenesis.
Abstract
Induction of neurogenesis can occur in the hippocampus in response to various pathological conditions, such as Alzheimer’s disease. The aim of this study was to investigate the changes that occur in endogenous neural stem cells in response to amyloid beta (Aβ)25-35-induced neuronal cell damage in organotypic hippocampal slice cultures. Cresyl violet staining and Fluoro-Jade B staining were used to detect neuronal cell damage and changes of mossy fiber terminals were observed by Timm’s staining. The immunofl uorescence staining was used to detect the newly generated cells in the subgranular zone (SGZ) of the dentate gyrus with specific marker, 5-bromo-2′-deoxyuridine (BrdU), Ki-67, Nestin, and doublecortin (DCX). In compared to control slices, neuronal cell damage was observed and the mossy fi bers were expanded to CA3 area by treatment with Aβ25-35. Ki-67/Nestin- and BrdU/DCX-positive cells were detected in the SGZ. In conclusion, these results demonstrate that Aβ-induced neuronal damage results in an increase in endogenous neural stem cells in rat hippocampal slice cultures not only for gliosis but also for neurogenesis.
참고문헌 (38)
- Bjorklund N L, "Absence of amyloid beta oligomers at the postsynapse and regulated synaptic Zn2+ in cognitively intact aged individuals with Alzheimer’s disease neuropathology", Mol. Neurodegener, 7, pp.23~ (2012)
- Bunk E C, "NMDAinduced injury of mouse organotypic hippocampal slice cultures triggers delayed neuroblast proliferation in the dentate gyrus: an in vitro model for the study of neural precursor cell proliferation", Brain Res, 1359, pp.22~32 (2010)
- Bush A I, "Rapid induction of Alzheimer A beta amyloid formation by zinc", Science, 265, pp.1464~1467 (1994)
- Chechneva O, "Identification and characterization of two neurogenic zones in interface organotypic hippocampal slice cultures", Neuroscience, 136, pp.343~355 (2005)
- Chuang T T, "Neurogenesis in mouse models of Alzheimer’s disease", BBA, 1802, pp.872~880 (2010)
- Dehghani F, "The immunosuppressant mycophenolate mofetil attenuates neuronal damage after excitotoxic injury in hippocampal slice cultures", Eur. J. Neurosci, 18, pp.1061~1072 (2003)
- Deshpande A, "A role for synaptic zinc in activity-dependent Abeta oligomer formation and accumulation at excitatory synapses", J. neurosci, 29, pp.4004~4015 (2009)
- Eriksson P S, "Neurogenesis in the adult human hippocampus", Nat. Med, 4, pp.1313~1317 (1998)
- Faller P, "Copper and zinc binding to amyloid-beta: coordination, dynamics, aggregation, reactivity and metal-ion transfer", Chembiochem: Eur. J. Chem. Biol, 10, pp.2837~2845 (2009)
- Haughey N J, "Disruption of neurogenesis in the subventricular zone of adult mice, and in human cortical neuronal precursor cells in culture, by amyloid beta-peptide: implications for the pathogenesis of Alzheimer’s disease", Neuromolecular Med, 1, pp.125~135 (2002)
- Haydar T F, "Organotypic slice cultures for analysis of proliferation, cell death, and migration in the embryonic neocortex", Brain Res, 4, pp.425~437 (1999)
- Heo C, "Effects of the monomeric, oligomeric, and fi brillar Abeta42 peptides on the proliferation and differentiation of adult neural stem cells from subventricular zone", J. Neurochem, 102, pp.493~500 (2007)
- Huang E P, "Metal ions and synaptic transmission: think zinc", Proc. Natl. Acad. Sci. U S A, 94, pp.13386~13387 (1997)
- Kuan C Y, "Hypoxia-ischemia induces DNA synthesis without cell proliferation in dying neurons in adult rodent brain", J. Neurosci, 24, pp.10763~10772 (2004)
- Lie D C, "Neurogenesis in the adult brain: new strategies for central nervous system diseases", Ann. Rev. Pharm. Toxicol, 44, pp.399~421 (2004)
- Lopez-Toledano M A, "Neurogenic effect of betaamyloid peptide in the development of neural stem cells", J. Neurosci, 24, pp.5439~5444 (2004)
- Lopez-Toledano M A, "Increased neurogenesis in young transgenic mice overexpressing human APP(Sw, Ind)", J. Alzheimer’s Dis, 12, pp.229~240 (2007)
- Mattson M P, "Apoptosis in neurodegenerative disorders", Nat. Rev. Mol. Cell Bio, 1, pp.120~129 (2000)
- Mazur-Kolecka B, "Amyloid-beta impairs development of neuronal progenitor cells by oxidative mechanisms", Neurobiol. Aging, 27, pp.1181~1192 (2006)
- Namba T, "Postnatal neurogenesis in hippocampal slice cultures: early in vitro labeling of neural precursor cells leads to efficient neuronal production", J. Neurosci. Res, 85, pp.1704~1712 (2007)
- Perez-Gomez A, "Enhanced neurogenesis in organotypic cultures of rat hippocampus after transient subfieldselective excitotoxic insult induced by domoic acid", Neuroscience, 208, pp.97~108 (2012)
- Picard-Riera N, "Endogenous adult neural stem cells: limits and potential to repair the injured central nervous system", J. Neurosci. Res, 76, pp.223~231 (2004)
- Plumpe T, "Variability of doublecortin-associated dendrite maturation in adult hippocampal neurogenesis is independent of the regulation of precursor cell proliferation", BMC Neurosci, 7, pp.77~ (2006)
- Raineteau O, "Neurogenesis in hippocampal slice cultures", Mol. Cell.Neurosci, 26, pp.241~250 (2004)
- Religa D, "Elevated cortical zinc in Alzheimer disease", Neurology, 67, pp.69~75 (2006)
- Rodriguez J J, "Impaired cell proliferation in the subventricular zone in an Alzheimer’s disease model", Neuroreport, 20, pp.907~912 (2009)
- Rola R, "Radiation-induced impairment of hippocampal neurogenesis is associated with cognitive defi cits in young mice", Exp. Neurol, 188, pp.316~330 (2004)
- Sadgrove M P, "Examination of granule layer cell count, cell density, and single-pulse BrdU incorporation in rat organotypic hippocampal slice cultures with respect to culture medium, septotemporal position, and time in vitro", J. Comp. Neurol, 497, pp.397~415 (2006)
- Scheffler B, "Functional network integration of embryonic stem cell-derived astrocytes in hippocampal slice cultures", Development (Cambridge, England), 130, pp.5533~5541 (2003)
- Schaffer D V, "Neurogenesis and neuroadaptation", Neuromolecular Med, 5, pp.1~9 (2004)
- Suh E C, "A beta 25-35 induces presynaptic changes in organotypic hippocampal slicecultures", Neurotoxicology, 29, pp.691~699 (2008)
- Tamura M, "K252a, an inhibitor of Trk, disturbs pathfinding of hippocampal mossy fi bers", Neuroreport, 17, pp.481~486 (2006)
- Tanaka A, "Immunohistochemical changes related to ageing in the mouse hippocampus and subventricular zone", Mech. Ageing Dev, 128, pp.303~310 (2007)
- Tanvig M, "A brain slice culture model for studies of endogenous and exogenous precursor cell migration in the rostral migratory stream", Brain Res, 1295, pp.1~12 (2009)
- Wang J M, "Regeneration in a degenerating brain: potential of allopregnanolone as a neuroregenerative agent", Curr. Alzheimer Res, 4, pp.510~517 (2007)
- Wang S H, "Hippocampal neurogenesis and behavioural studies on adult ischemic rat response to chronic mild stress", Behav. Brain Res, 189, pp.9~16 (2008)
- Zhang C, "Long-lasting impairment in hippocampal neurogenesis associated with amyloid deposition in a knock-in mouse model of familial Alzheimer’s disease", Exp. Neurol, 204, pp.77~87 (2007)
- Ziabreva I, "Altered neurogenesis in Alzheimer’s disease", J. Psychosom. Res, 61, pp.311~316 (2006)
