Skip to main content
Erschienen in: Neuroscience Bulletin 2/2019

01.04.2019 | Review

Human Brain Slice Culture: A Useful Tool to Study Brain Disorders and Potential Therapeutic Compounds

verfasst von: Xin-Rui Qi, Ronald W. H. Verwer, Ai-Min Bao, Rawien A. Balesar, Sabina Luchetti, Jiang-Ning Zhou, Dick F. Swaab

Erschienen in: Neuroscience Bulletin | Ausgabe 2/2019

Einloggen, um Zugang zu erhalten

Abstract

Investigating the pathophysiological mechanisms underlying brain disorders is a priority if novel therapeutic strategies are to be developed. In vivo studies of animal models and in vitro studies of cell lines/primary cell cultures may provide useful tools to study certain aspects of brain disorders. However, discrepancies among these studies or unsuccessful translation from animal/cell studies to human/clinical studies often occur, because these models generally represent only some symptoms of a neuropsychiatric disorder rather than the complete disorder. Human brain slice cultures from postmortem tissue or resected tissue from operations have shown that, in vitro, neurons and glia can stay alive for long periods of time, while their morphological and physiological characteristics, and their ability to respond to experimental manipulations are maintained. Human brain slices can thus provide a close representation of neuronal networks in vivo, be a valuable tool for investigation of the basis of neuropsychiatric disorders, and provide a platform for the evaluation of novel pharmacological treatments of human brain diseases. A brain bank needs to provide the necessary infrastructure to bring together donors, hospitals, and researchers who want to investigate human brain slices in cultures of clinically and neuropathologically well-documented material.
Literatur
1.
Zurück zum Zitat Drummond E, Wisniewski T. Alzheimer’s disease: experimental models and reality. Acta Neuropathol 2017, 133: 155–175.CrossRefPubMed Drummond E, Wisniewski T. Alzheimer’s disease: experimental models and reality. Acta Neuropathol 2017, 133: 155–175.CrossRefPubMed
2.
Zurück zum Zitat Nader MA. Animal models for addiction medicine: From vulnerable phenotypes to addicted individuals. Prog Brain Res 2016, 224: 3–24.CrossRefPubMed Nader MA. Animal models for addiction medicine: From vulnerable phenotypes to addicted individuals. Prog Brain Res 2016, 224: 3–24.CrossRefPubMed
3.
Zurück zum Zitat Czeh B, Fuchs E, Wiborg O, Simon M. Animal models of major depression and their clinical implications. Prog Neuropsychopharmacol Biol Psychiatry 2016, 64: 293–310.CrossRefPubMed Czeh B, Fuchs E, Wiborg O, Simon M. Animal models of major depression and their clinical implications. Prog Neuropsychopharmacol Biol Psychiatry 2016, 64: 293–310.CrossRefPubMed
4.
Zurück zum Zitat Willner P. Validity, reliability and utility of the chronic mild stress model of depression: a 10-year review and evaluation. Psychopharmacology (Berl) 1997, 134: 319–329.CrossRef Willner P. Validity, reliability and utility of the chronic mild stress model of depression: a 10-year review and evaluation. Psychopharmacology (Berl) 1997, 134: 319–329.CrossRef
5.
Zurück zum Zitat Sasaguri H, Nilsson P, Hashimoto S, Nagata K, Saito T, De Strooper B, et al. APP mouse models for Alzheimer’s disease preclinical studies. EMBO J 2017, 36: 2473–2487.CrossRefPubMedPubMedCentral Sasaguri H, Nilsson P, Hashimoto S, Nagata K, Saito T, De Strooper B, et al. APP mouse models for Alzheimer’s disease preclinical studies. EMBO J 2017, 36: 2473–2487.CrossRefPubMedPubMedCentral
6.
Zurück zum Zitat Testa-Silva G, Verhoog MB, Linaro D, de Kock CP, Baayen JC, Meredith RM, et al. High bandwidth synaptic communication and frequency tracking in human neocortex. PLoS Biol 2014, 12: e1002007.CrossRefPubMedPubMedCentral Testa-Silva G, Verhoog MB, Linaro D, de Kock CP, Baayen JC, Meredith RM, et al. High bandwidth synaptic communication and frequency tracking in human neocortex. PLoS Biol 2014, 12: e1002007.CrossRefPubMedPubMedCentral
7.
Zurück zum Zitat Verhoog MB, Goriounova NA, Obermayer J, Stroeder J, Hjorth JJ, Testa-Silva G, et al. Mechanisms underlying the rules for associative plasticity at adult human neocortical synapses. J Neurosci 2013, 33: 17197–17208.CrossRefPubMedPubMedCentral Verhoog MB, Goriounova NA, Obermayer J, Stroeder J, Hjorth JJ, Testa-Silva G, et al. Mechanisms underlying the rules for associative plasticity at adult human neocortical synapses. J Neurosci 2013, 33: 17197–17208.CrossRefPubMedPubMedCentral
8.
Zurück zum Zitat Oberheim NA, Wang XH, Goldman S, Nedergaard M. Astrocytic complexity distinguishes the human brain. Trends Neurosci 2006, 29: 547–553.CrossRefPubMed Oberheim NA, Wang XH, Goldman S, Nedergaard M. Astrocytic complexity distinguishes the human brain. Trends Neurosci 2006, 29: 547–553.CrossRefPubMed
9.
Zurück zum Zitat Oberheim NA, Takano T, Han X, He W, Lin JHC, Wang F, et al. Uniquely hominid features of adult human astrocytes. J Neurosci 2009, 29: 3276–3287.CrossRefPubMedPubMedCentral Oberheim NA, Takano T, Han X, He W, Lin JHC, Wang F, et al. Uniquely hominid features of adult human astrocytes. J Neurosci 2009, 29: 3276–3287.CrossRefPubMedPubMedCentral
10.
Zurück zum Zitat Van Dam D, De Deyn PP. Non human primate models for Alzheimer’s disease-related research and drug discovery. Expert Opin Drug Discov 2017, 12: 187–200. Van Dam D, De Deyn PP. Non human primate models for Alzheimer’s disease-related research and drug discovery. Expert Opin Drug Discov 2017, 12: 187–200.
11.
Zurück zum Zitat Bauman MD, Schumann CM. Advances in nonhuman primate models of autism: Integrating neuroscience and behavior. Exp Neurol 2018, 299: 252–265.CrossRefPubMed Bauman MD, Schumann CM. Advances in nonhuman primate models of autism: Integrating neuroscience and behavior. Exp Neurol 2018, 299: 252–265.CrossRefPubMed
12.
Zurück zum Zitat Willner P. The validity of animal models of depression. Psychopharmacology (Berl) 1984, 83: 1–16.CrossRef Willner P. The validity of animal models of depression. Psychopharmacology (Berl) 1984, 83: 1–16.CrossRef
13.
Zurück zum Zitat Valster A, Tran NL, Nakada M, Berens ME, Chan AY, Symons M. Cell migration and invasion assays. Methods 2005, 37: 208–215.CrossRefPubMed Valster A, Tran NL, Nakada M, Berens ME, Chan AY, Symons M. Cell migration and invasion assays. Methods 2005, 37: 208–215.CrossRefPubMed
14.
Zurück zum Zitat Buendia I, Parada E, Navarro E, Leon R, Negredo P, Egea J, et al. Subthreshold concentrations of melatonin and galantamine improves pathological AD-hallmarks in hippocampal organotypic cultures. Mol Neurobiol 2016, 53: 3338–3348.CrossRefPubMed Buendia I, Parada E, Navarro E, Leon R, Negredo P, Egea J, et al. Subthreshold concentrations of melatonin and galantamine improves pathological AD-hallmarks in hippocampal organotypic cultures. Mol Neurobiol 2016, 53: 3338–3348.CrossRefPubMed
15.
Zurück zum Zitat Shahani N, Subramaniam S, Wolf T, Tackenberg C, Brandt R. Tau aggregation and progressive neuronal degeneration in the absence of changes in spine density and morphology after targeted expression of Alzheimer’s disease-relevant tau constructs in organotypic hippocampal slices. J Neurosci 2006, 26: 6103–6114.CrossRefPubMedPubMedCentral Shahani N, Subramaniam S, Wolf T, Tackenberg C, Brandt R. Tau aggregation and progressive neuronal degeneration in the absence of changes in spine density and morphology after targeted expression of Alzheimer’s disease-relevant tau constructs in organotypic hippocampal slices. J Neurosci 2006, 26: 6103–6114.CrossRefPubMedPubMedCentral
16.
Zurück zum Zitat Cartier J, Piyasena C, Sparrow SA, Boardman JP, Drake AJ. Alterations in glucose concentrations affect DNA methylation at Lrg1 in an ex vivo rat cortical slice model of preterm brain injury. Eur J Neurosci 2018, 47: 380–387.CrossRefPubMed Cartier J, Piyasena C, Sparrow SA, Boardman JP, Drake AJ. Alterations in glucose concentrations affect DNA methylation at Lrg1 in an ex vivo rat cortical slice model of preterm brain injury. Eur J Neurosci 2018, 47: 380–387.CrossRefPubMed
17.
Zurück zum Zitat Molnar G, Rozsa M, Baka J, Holderith N, Barzo P, Nusser Z, et al. Human pyramidal to interneuron synapses are mediated by multi-vesicular release and multiple docked vesicles. Elife 2016, 5. Molnar G, Rozsa M, Baka J, Holderith N, Barzo P, Nusser Z, et al. Human pyramidal to interneuron synapses are mediated by multi-vesicular release and multiple docked vesicles. Elife 2016, 5.
18.
Zurück zum Zitat Konishi Y, Lindholm K, Yang LB, Li R, Shen Y. Isolation of living neurons from human elderly brains using the immunomagnetic sorting DNA-linker system. Am J Pathol 2002, 161: 1567–1576.CrossRefPubMedPubMedCentral Konishi Y, Lindholm K, Yang LB, Li R, Shen Y. Isolation of living neurons from human elderly brains using the immunomagnetic sorting DNA-linker system. Am J Pathol 2002, 161: 1567–1576.CrossRefPubMedPubMedCentral
19.
Zurück zum Zitat Kriks S, Shim JW, Piao J, Ganat YM, Wakeman DR, Xie Z, et al. Dopamine neurons derived from human ES cells efficiently engraft in animal models of Parkinson’s disease. Nature 2011, 480: 547–551.CrossRefPubMedPubMedCentral Kriks S, Shim JW, Piao J, Ganat YM, Wakeman DR, Xie Z, et al. Dopamine neurons derived from human ES cells efficiently engraft in animal models of Parkinson’s disease. Nature 2011, 480: 547–551.CrossRefPubMedPubMedCentral
20.
Zurück zum Zitat Zhang Y, Pak C, Han Y, Ahlenius H, Zhang Z, Chanda S, et al. Rapid single-step induction of functional neurons from human pluripotent stem cells. Neuron 2013, 78: 785–798.CrossRefPubMedPubMedCentral Zhang Y, Pak C, Han Y, Ahlenius H, Zhang Z, Chanda S, et al. Rapid single-step induction of functional neurons from human pluripotent stem cells. Neuron 2013, 78: 785–798.CrossRefPubMedPubMedCentral
21.
Zurück zum Zitat Lancaster MA, Renner M, Martin CA, Wenzel D, Bicknell LS, Hurles ME, et al. Cerebral organoids model human brain development and microcephaly. Nature 2013, 501: 373–379.CrossRefPubMed Lancaster MA, Renner M, Martin CA, Wenzel D, Bicknell LS, Hurles ME, et al. Cerebral organoids model human brain development and microcephaly. Nature 2013, 501: 373–379.CrossRefPubMed
22.
Zurück zum Zitat Qi XR, Luchetti S, Verwer RWH, Sluiter AA, Mason MRJ, Zhou JN, et al. Alterations in the steroid biosynthetic pathways in the human prefrontal cortex in mood disorders: A post-mortem study. Brain Pathol 2018, 28: 536–547.CrossRefPubMed Qi XR, Luchetti S, Verwer RWH, Sluiter AA, Mason MRJ, Zhou JN, et al. Alterations in the steroid biosynthetic pathways in the human prefrontal cortex in mood disorders: A post-mortem study. Brain Pathol 2018, 28: 536–547.CrossRefPubMed
23.
Zurück zum Zitat Verwer RW, Baker RE, Boiten EF, Dubelaar EJ, van Ginkel CJ, Sluiter AA, et al. Post-mortem brain tissue cultures from elderly control subjects and patients with a neurodegenerative disease. Exp Gerontol 2003, 38: 167–172.CrossRefPubMed Verwer RW, Baker RE, Boiten EF, Dubelaar EJ, van Ginkel CJ, Sluiter AA, et al. Post-mortem brain tissue cultures from elderly control subjects and patients with a neurodegenerative disease. Exp Gerontol 2003, 38: 167–172.CrossRefPubMed
24.
Zurück zum Zitat Verwer RW, Hermens WT, Dijkhuizen P, ter Brake O, Baker RE, Salehi A, et al. Cells in human postmortem brain tissue slices remain alive for several weeks in culture. FASEB J 2002, 16: 54–60.CrossRefPubMed Verwer RW, Hermens WT, Dijkhuizen P, ter Brake O, Baker RE, Salehi A, et al. Cells in human postmortem brain tissue slices remain alive for several weeks in culture. FASEB J 2002, 16: 54–60.CrossRefPubMed
25.
Zurück zum Zitat Verwer RW, Sluiter AA, Balesar RA, Baaijen JC, de Witt Hamer PC, Speijer D, et al. Injury response of resected human brain tissue in vitro. Brain Pathol 2015, 25: 454–468.CrossRefPubMed Verwer RW, Sluiter AA, Balesar RA, Baaijen JC, de Witt Hamer PC, Speijer D, et al. Injury response of resected human brain tissue in vitro. Brain Pathol 2015, 25: 454–468.CrossRefPubMed
26.
Zurück zum Zitat Verwer RW, Sluiter AA, Balesar RA, Baayen JC, Noske DP, Dirven CM, et al. Mature astrocytes in the adult human neocortex express the early neuronal marker doublecortin. Brain 2007, 130: 3321–3335.CrossRefPubMed Verwer RW, Sluiter AA, Balesar RA, Baayen JC, Noske DP, Dirven CM, et al. Mature astrocytes in the adult human neocortex express the early neuronal marker doublecortin. Brain 2007, 130: 3321–3335.CrossRefPubMed
27.
Zurück zum Zitat Verwer RW, Sluiter AA, Balesar RA, Baayen JC, Speijer D, Idema S, et al. Altered loyalties of neuronal markers in cultured slices of resected human brain tissue. Brain Pathol 2016, 26: 523–532.CrossRefPubMed Verwer RW, Sluiter AA, Balesar RA, Baayen JC, Speijer D, Idema S, et al. Altered loyalties of neuronal markers in cultured slices of resected human brain tissue. Brain Pathol 2016, 26: 523–532.CrossRefPubMed
28.
Zurück zum Zitat Wu L, Sluiter AA, Guo HF, Balesar RA, Swaab DF, Zhou JN, et al. Neural stem cells improve neuronal survival in cultured postmortem brain tissue from aged and Alzheimer patients. J Cell Mol Med 2008, 12: 1611–1621.CrossRefPubMed Wu L, Sluiter AA, Guo HF, Balesar RA, Swaab DF, Zhou JN, et al. Neural stem cells improve neuronal survival in cultured postmortem brain tissue from aged and Alzheimer patients. J Cell Mol Med 2008, 12: 1611–1621.CrossRefPubMed
29.
Zurück zum Zitat Castren E, Rantamaki T. The role of BDNF and its receptors in depression and antidepressant drug action: Reactivation of developmental plasticity. Dev Neurobiol 2010, 70: 289–297.CrossRefPubMed Castren E, Rantamaki T. The role of BDNF and its receptors in depression and antidepressant drug action: Reactivation of developmental plasticity. Dev Neurobiol 2010, 70: 289–297.CrossRefPubMed
30.
Zurück zum Zitat Martinowich K, Manji H, Lu B. New insights into BDNF function in depression and anxiety. Nat Neurosci 2007, 10: 1089–1093.CrossRefPubMed Martinowich K, Manji H, Lu B. New insights into BDNF function in depression and anxiety. Nat Neurosci 2007, 10: 1089–1093.CrossRefPubMed
31.
Zurück zum Zitat Wolkowitz OM, Reus VI, Keebler A, Nelson N, Friedland M, Brizendine L, et al. Double-blind treatment of major depression with dehydroepiandrosterone. Am J Psychiatry 1999, 156: 646–649.PubMed Wolkowitz OM, Reus VI, Keebler A, Nelson N, Friedland M, Brizendine L, et al. Double-blind treatment of major depression with dehydroepiandrosterone. Am J Psychiatry 1999, 156: 646–649.PubMed
32.
Zurück zum Zitat Rabkin JG, McElhiney MC, Rabkin R, McGrath PJ, Ferrando SJ. Placebo-controlled trial of dehydroepiandrosterone (DHEA) for treatment of nonmajor depression in patients with HIV/AIDS. Am J Psychiatry 2006, 163: 59–66.CrossRefPubMed Rabkin JG, McElhiney MC, Rabkin R, McGrath PJ, Ferrando SJ. Placebo-controlled trial of dehydroepiandrosterone (DHEA) for treatment of nonmajor depression in patients with HIV/AIDS. Am J Psychiatry 2006, 163: 59–66.CrossRefPubMed
33.
Zurück zum Zitat Bsibsi M, Persoon-Deen C, Verwer RW, Meeuwsen S, Ravid R, Van Noort JM. Toll-like receptor 3 on adult human astrocytes triggers production of neuroprotective mediators. Glia 2006, 53: 688–695.CrossRefPubMed Bsibsi M, Persoon-Deen C, Verwer RW, Meeuwsen S, Ravid R, Van Noort JM. Toll-like receptor 3 on adult human astrocytes triggers production of neuroprotective mediators. Glia 2006, 53: 688–695.CrossRefPubMed
34.
Zurück zum Zitat Talbot K, Wang HY, Kazi H, Han LY, Bakshi KP, Stucky A, et al. Demonstrated brain insulin resistance in Alzheimer’s disease patients is associated with IGF-1 resistance, IRS-1 dysregulation, and cognitive decline. J Clin Invest 2012, 122: 1316–1338.CrossRefPubMedPubMedCentral Talbot K, Wang HY, Kazi H, Han LY, Bakshi KP, Stucky A, et al. Demonstrated brain insulin resistance in Alzheimer’s disease patients is associated with IGF-1 resistance, IRS-1 dysregulation, and cognitive decline. J Clin Invest 2012, 122: 1316–1338.CrossRefPubMedPubMedCentral
35.
Zurück zum Zitat Dai JP, Swaab DF, Buijs RM. Recovery of axonal transport in “dead neurons”. Lancet 1998, 351: 499–500.CrossRefPubMed Dai JP, Swaab DF, Buijs RM. Recovery of axonal transport in “dead neurons”. Lancet 1998, 351: 499–500.CrossRefPubMed
36.
Zurück zum Zitat Dai JP, Van der Vliet J, Swaab DF, Buijs RM. Human retinohypothalamic tract as revealed by in vitro postmortem tracing. J Comp Neurol 1998, 397: 357–370.CrossRefPubMed Dai JP, Van der Vliet J, Swaab DF, Buijs RM. Human retinohypothalamic tract as revealed by in vitro postmortem tracing. J Comp Neurol 1998, 397: 357–370.CrossRefPubMed
37.
Zurück zum Zitat Dai JP, Swaab DF, Van der Vliet J, Buijs RM. Postmortem tracing reveals the organization of hypothalamic projections of the suprachiasmatic nucleus in the human brain. J Comp Neurol 1998, 400: 87–102.CrossRefPubMed Dai JP, Swaab DF, Van der Vliet J, Buijs RM. Postmortem tracing reveals the organization of hypothalamic projections of the suprachiasmatic nucleus in the human brain. J Comp Neurol 1998, 400: 87–102.CrossRefPubMed
38.
Zurück zum Zitat Dai JP, Van der Vliet J, Swaab DF, Buijs RM. Postmortem anterograde tracing of intrahypothalamic projections of the human dorsomedial nucleus of the hypothalamus. J Comp Neurol 1998, 401: 16–33.CrossRefPubMed Dai JP, Van der Vliet J, Swaab DF, Buijs RM. Postmortem anterograde tracing of intrahypothalamic projections of the human dorsomedial nucleus of the hypothalamus. J Comp Neurol 1998, 401: 16–33.CrossRefPubMed
39.
Zurück zum Zitat Dai JP, Buijs RM, Kamphorst W, Swaab DF. Impaired axonal transport of cortical neurons in Alzheimer’s disease is associated with neuropathological changes. Brain Res 2002, 948: 138–144.CrossRefPubMed Dai JP, Buijs RM, Kamphorst W, Swaab DF. Impaired axonal transport of cortical neurons in Alzheimer’s disease is associated with neuropathological changes. Brain Res 2002, 948: 138–144.CrossRefPubMed
40.
Zurück zum Zitat Dai JP, Buijs R, Swaab D. Glucocorticoid hormone (cortisol) affects axonal transport in human cortex neurons but shows resistance in Alzheimer’s disease. Br J Pharmacol 2004, 143: 606–610.CrossRefPubMedPubMedCentral Dai JP, Buijs R, Swaab D. Glucocorticoid hormone (cortisol) affects axonal transport in human cortex neurons but shows resistance in Alzheimer’s disease. Br J Pharmacol 2004, 143: 606–610.CrossRefPubMedPubMedCentral
41.
Zurück zum Zitat Schwarz N, Hedrich UBS, Schwarz H, P AH, Dammeier N, Auffenberg E, et al. Human cerebrospinal fluid promotes long-term neuronal viability and network function in human neocortical organotypic brain slice cultures. Sci Rep 2017, 7: 12249. Schwarz N, Hedrich UBS, Schwarz H, P AH, Dammeier N, Auffenberg E, et al. Human cerebrospinal fluid promotes long-term neuronal viability and network function in human neocortical organotypic brain slice cultures. Sci Rep 2017, 7: 12249.
42.
Zurück zum Zitat Wickham J, Brodjegard NG, Vighagen R, Pinborg LH, Bengzon J, Woldbye DPD, et al. Prolonged life of human acute hippocampal slices from temporal lobe epilepsy surgery. Sci Rep 2018, 8: 4158.CrossRefPubMedPubMedCentral Wickham J, Brodjegard NG, Vighagen R, Pinborg LH, Bengzon J, Woldbye DPD, et al. Prolonged life of human acute hippocampal slices from temporal lobe epilepsy surgery. Sci Rep 2018, 8: 4158.CrossRefPubMedPubMedCentral
43.
Zurück zum Zitat Le Duigou C, Savary E, Morin-Brureau M, Gomez-Dominguez D, Sobczyk A, Chali F, et al. Imaging pathological activities of human brain tissue in organotypic culture. J Neurosci Methods 2018, 298: 33–44.CrossRefPubMedPubMedCentral Le Duigou C, Savary E, Morin-Brureau M, Gomez-Dominguez D, Sobczyk A, Chali F, et al. Imaging pathological activities of human brain tissue in organotypic culture. J Neurosci Methods 2018, 298: 33–44.CrossRefPubMedPubMedCentral
44.
Zurück zum Zitat Cohen I, Navarro V, Clemenceau S, Baulac M, Miles R. On the origin of interictal activity in human temporal lobe epilepsy in vitro. Science 2002, 298: 1418–1421.CrossRefPubMed Cohen I, Navarro V, Clemenceau S, Baulac M, Miles R. On the origin of interictal activity in human temporal lobe epilepsy in vitro. Science 2002, 298: 1418–1421.CrossRefPubMed
45.
Zurück zum Zitat Mendes ND, Fernandes A, Almeida GM, Santos LE, Selles MC, Lyra ESNM, et al. Free-floating adult human brain-derived slice cultures as a model to study the neuronal impact of Alzheimer’s disease-associated Abeta oligomers. J Neurosci Methods 2018, 307: 203–209.CrossRefPubMed Mendes ND, Fernandes A, Almeida GM, Santos LE, Selles MC, Lyra ESNM, et al. Free-floating adult human brain-derived slice cultures as a model to study the neuronal impact of Alzheimer’s disease-associated Abeta oligomers. J Neurosci Methods 2018, 307: 203–209.CrossRefPubMed
46.
Zurück zum Zitat Sebollela A, Freitas-Correa L, Oliveira FF, Paula-Lima AC, Saraiva LM, Martins SM, et al. Amyloid-beta oligomers induce differential gene expression in adult human brain slices. J Biol Chem 2012, 287: 7436–7445.CrossRefPubMedPubMedCentral Sebollela A, Freitas-Correa L, Oliveira FF, Paula-Lima AC, Saraiva LM, Martins SM, et al. Amyloid-beta oligomers induce differential gene expression in adult human brain slices. J Biol Chem 2012, 287: 7436–7445.CrossRefPubMedPubMedCentral
47.
Zurück zum Zitat Chaichana KL, Capilla-Gonzalez V, Gonzalez-Perez O, Pradilla G, Han J, Olivi A, et al. Preservation of glial cytoarchitecture from ex vivo human tumor and non-tumor cerebral cortical explants: A human model to study neurological diseases. J Neurosci Methods 2007, 164: 261–270.CrossRefPubMedPubMedCentral Chaichana KL, Capilla-Gonzalez V, Gonzalez-Perez O, Pradilla G, Han J, Olivi A, et al. Preservation of glial cytoarchitecture from ex vivo human tumor and non-tumor cerebral cortical explants: A human model to study neurological diseases. J Neurosci Methods 2007, 164: 261–270.CrossRefPubMedPubMedCentral
48.
Zurück zum Zitat Ting JT, Kalmbach B, Chong P, de Frates R, Keene CD, Gwinn RP, et al. A robust ex vivo experimental platform for molecular-genetic dissection of adult human neocortical cell types and circuits. Sci Rep 2018, 8: 8407.CrossRefPubMedPubMedCentral Ting JT, Kalmbach B, Chong P, de Frates R, Keene CD, Gwinn RP, et al. A robust ex vivo experimental platform for molecular-genetic dissection of adult human neocortical cell types and circuits. Sci Rep 2018, 8: 8407.CrossRefPubMedPubMedCentral
49.
Zurück zum Zitat Andersson M, Avaliani N, Svensson A, Wickham J, Pinborg LH, Jespersen B, et al. Optogenetic control of human neurons in organotypic brain cultures. Sci Rep 2016, 6. Andersson M, Avaliani N, Svensson A, Wickham J, Pinborg LH, Jespersen B, et al. Optogenetic control of human neurons in organotypic brain cultures. Sci Rep 2016, 6.
50.
Zurück zum Zitat Lavenex P, Lavenex PB, Bennett JL, Amaral DG. Postmortem changes in the neuroanatomical characteristics of the primate brain: hippocampal formation. J Comp Neurol 2009, 512: 27–51.CrossRefPubMedPubMedCentral Lavenex P, Lavenex PB, Bennett JL, Amaral DG. Postmortem changes in the neuroanatomical characteristics of the primate brain: hippocampal formation. J Comp Neurol 2009, 512: 27–51.CrossRefPubMedPubMedCentral
51.
Zurück zum Zitat Fountoulakis M, Hardmeier R, Hoger H, Lubec G. Postmortem changes in the level of brain proteins. Exp Neurol 2001, 167: 86–94.CrossRefPubMed Fountoulakis M, Hardmeier R, Hoger H, Lubec G. Postmortem changes in the level of brain proteins. Exp Neurol 2001, 167: 86–94.CrossRefPubMed
52.
Zurück zum Zitat Bao AM, Swaab DF. The art of matching brain tissue from patients and controls for postmortem research. Handb Clin Neurol 2018, 150: 197–217.CrossRefPubMed Bao AM, Swaab DF. The art of matching brain tissue from patients and controls for postmortem research. Handb Clin Neurol 2018, 150: 197–217.CrossRefPubMed
53.
Zurück zum Zitat Samarasekera N, Salman RA, Huitinga I, Klioueva N, McLean CA, Kretzschmar H, et al. Brain banking for neurological disorders. Lancet Neurol 2013, 12: 1096–1105.CrossRefPubMed Samarasekera N, Salman RA, Huitinga I, Klioueva N, McLean CA, Kretzschmar H, et al. Brain banking for neurological disorders. Lancet Neurol 2013, 12: 1096–1105.CrossRefPubMed
54.
Zurück zum Zitat Yan XX, Ma C, Bao AM, Wang XM, Gai WP. Brain banking as a cornerstone of neuroscience in China. Lancet Neurol 2015, 14: 136.CrossRefPubMed Yan XX, Ma C, Bao AM, Wang XM, Gai WP. Brain banking as a cornerstone of neuroscience in China. Lancet Neurol 2015, 14: 136.CrossRefPubMed
Metadaten
Titel
Human Brain Slice Culture: A Useful Tool to Study Brain Disorders and Potential Therapeutic Compounds
verfasst von
Xin-Rui Qi
Ronald W. H. Verwer
Ai-Min Bao
Rawien A. Balesar
Sabina Luchetti
Jiang-Ning Zhou
Dick F. Swaab
Publikationsdatum
01.04.2019
Verlag
Springer Singapore
Erschienen in
Neuroscience Bulletin / Ausgabe 2/2019
Print ISSN: 1673-7067
Elektronische ISSN: 1995-8218
DOI
https://doi.org/10.1007/s12264-018-0328-1

Weitere Artikel der Ausgabe 2/2019

Neuroscience Bulletin 2/2019 Zur Ausgabe

Leitlinien kompakt für die Neurologie

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Hirnblutung unter DOAK und VKA ähnlich bedrohlich

17.05.2024 Direkte orale Antikoagulanzien Nachrichten

Kommt es zu einer nichttraumatischen Hirnblutung, spielt es keine große Rolle, ob die Betroffenen zuvor direkt wirksame orale Antikoagulanzien oder Marcumar bekommen haben: Die Prognose ist ähnlich schlecht.

Thrombektomie auch bei großen Infarkten von Vorteil

16.05.2024 Ischämischer Schlaganfall Nachrichten

Auch ein sehr ausgedehnter ischämischer Schlaganfall scheint an sich kein Grund zu sein, von einer mechanischen Thrombektomie abzusehen. Dafür spricht die LASTE-Studie, an der Patienten und Patientinnen mit einem ASPECTS von maximal 5 beteiligt waren.

Schwindelursache: Massagepistole lässt Otholiten tanzen

14.05.2024 Benigner Lagerungsschwindel Nachrichten

Wenn jüngere Menschen über ständig rezidivierenden Lagerungsschwindel klagen, könnte eine Massagepistole der Auslöser sein. In JAMA Otolaryngology warnt ein Team vor der Anwendung hochpotenter Geräte im Bereich des Nackens.

Schützt Olivenöl vor dem Tod durch Demenz?

10.05.2024 Morbus Alzheimer Nachrichten

Konsumieren Menschen täglich 7 Gramm Olivenöl, ist ihr Risiko, an einer Demenz zu sterben, um mehr als ein Viertel reduziert – und dies weitgehend unabhängig von ihrer sonstigen Ernährung. Dafür sprechen Auswertungen zweier großer US-Studien.

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.