Home > Publications Database > Three-Dimensional Biohybrid StarPEG-Heparin Hydrogel Cultures for Modeling Human Neuronal Development and Alzheimer's Disease Pathology. > print |
001 | 165568 | ||
005 | 20240112171940.0 | ||
020 | _ | _ | |a 978-1-0716-2654-2 (print) |
020 | _ | _ | |a 978-1-0716-2655-9 (electronic) |
024 | 7 | _ | |a 10.1007/978-1-0716-2655-9_8 |2 doi |
024 | 7 | _ | |a pmid:36399269 |2 pmid |
024 | 7 | _ | |a 1064-3745 |2 ISSN |
024 | 7 | _ | |a 1940-6029 |2 ISSN |
024 | 7 | _ | |a altmetric:138628551 |2 altmetric |
037 | _ | _ | |a DZNE-2022-01708 |
041 | _ | _ | |a English |
082 | _ | _ | |a 570 |
100 | 1 | _ | |a Siddiqui, Tohid |0 P:(DE-2719)2812737 |b 0 |e First author |
245 | _ | _ | |a Three-Dimensional Biohybrid StarPEG-Heparin Hydrogel Cultures for Modeling Human Neuronal Development and Alzheimer's Disease Pathology. |
260 | _ | _ | |a New York, NY |c 2023 |b Springer US |
295 | 1 | 0 | |a Alzheimer’s Disease / Chun, Jerold (Editor) ; New York, NY : Springer US, 2023, Chapter 8 ; ISSN: 1064-3745=1940-6029 ; ISBN: 978-1-0716-2654-2=978-1-0716-2655-9 ; doi:10.1007/978-1-0716-2655-9 |
300 | _ | _ | |a 159 - 170 |
336 | 7 | _ | |a BOOK_CHAPTER |2 ORCID |
336 | 7 | _ | |a Book Section |0 7 |2 EndNote |
336 | 7 | _ | |a bookPart |2 DRIVER |
336 | 7 | _ | |a INBOOK |2 BibTeX |
336 | 7 | _ | |a Output Types/Book chapter |2 DataCite |
336 | 7 | _ | |a Contribution to a book |b contb |m contb |0 PUB:(DE-HGF)7 |s 1694166854_31831 |2 PUB:(DE-HGF) |
490 | 0 | _ | |a Methods in Molecular Biology |v 2561 |
520 | _ | _ | |a In this chapter, we present the methodology currently used in our laboratory to generate a starPEG-MMP (starPEG)- and heparin maleimide HM06 (heparin)-based 3D cell culture system, in a hydrogel, that can be used to study human neuronal development and Alzheimer's disease (AD) pathology. A 3D cell culture system can mimic the in vivo cellular environment better than a 2D format, in which these cells exhibit neural network formation, electrophysiological activity, tissue-specific extracellular matrix (ECM) deposition, and neurotransmitter responsiveness. When treated with amyloid beta-42 (Aβ42) peptides, this system recapitulates many of the pathological effects of AD, including reduced neural stem cell proliferation, impaired neuronal network formation, dystrophic axonal ends, synaptic loss, failure to deposit ECM, elevated tau hyperphosphorylation, and formation of neurofibrillary tangles. Culturing human primary cortical astrocyte (pHA)- or induced pluripotent stem cell (iPSC)-derived human neural stem cells in this biohybrid hydrogel system has led to the discovery of novel regulatory pathways underlying neurodegenerative pathology in different phases of AD. |
536 | _ | _ | |a 352 - Disease Mechanisms (POF4-352) |0 G:(DE-HGF)POF4-352 |c POF4-352 |f POF IV |x 0 |
588 | _ | _ | |a Dataset connected to CrossRef Book Series, PubMed, , Journals: pub.dzne.de |
650 | _ | 2 | |a Humans |2 MeSH |
650 | _ | 2 | |a Alzheimer Disease: metabolism |2 MeSH |
650 | _ | 2 | |a Amyloid beta-Peptides: metabolism |2 MeSH |
650 | _ | 2 | |a Hydrogels: metabolism |2 MeSH |
650 | _ | 2 | |a Heparin: metabolism |2 MeSH |
650 | _ | 2 | |a Neurons: metabolism |2 MeSH |
650 | _ | 7 | |a Alzheimer’s disease |2 Other |
650 | _ | 7 | |a 3D |2 Other |
650 | _ | 7 | |a Alzheimer’s disease |2 Other |
650 | _ | 7 | |a Amyloid beta-42 (Aβ42) |2 Other |
650 | _ | 7 | |a Biohybrid hydrogel cell culture |2 Other |
650 | _ | 7 | |a Heparin |2 Other |
650 | _ | 7 | |a Human neural development |2 Other |
650 | _ | 7 | |a Primary human astrocytes |2 Other |
650 | _ | 7 | |a StarPEG |2 Other |
650 | _ | 7 | |a iPSC-derived neural stem cells |2 Other |
650 | _ | 7 | |a Amyloid beta-Peptides |2 NLM Chemicals |
650 | _ | 7 | |a Hydrogels |2 NLM Chemicals |
650 | _ | 7 | |a Heparin |0 9005-49-6 |2 NLM Chemicals |
650 | _ | 7 | |a Amyloid beta-42 (Aβ42) |2 Other |
700 | 1 | _ | |a Celikkaya, Hilal |0 P:(DE-2719)2813050 |b 1 |
700 | 1 | _ | |a Atasavum, Zeynep Tansu |0 P:(DE-2719)9002487 |b 2 |u dzne |
700 | 1 | _ | |a Popova, Stanislava |0 P:(DE-2719)2812472 |b 3 |
700 | 1 | _ | |a Freudenberg, Uwe |b 4 |
700 | 1 | _ | |a Werner, Carsten |b 5 |
700 | 1 | _ | |a Kizil, Caghan |0 P:(DE-2719)2811030 |b 6 |e Last author |
773 | _ | _ | |a 10.1007/978-1-0716-2655-9_8 |
856 | 4 | _ | |u https://pub.dzne.de/record/165568/files/DZNE-2022-01708_Restricted.pdf |
856 | 4 | _ | |u https://pub.dzne.de/record/165568/files/DZNE-2022-01708_Restricted.pdf?subformat=pdfa |x pdfa |
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910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 0 |6 P:(DE-2719)2812737 |
910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 1 |6 P:(DE-2719)2813050 |
910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 2 |6 P:(DE-2719)9002487 |
910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 3 |6 P:(DE-2719)2812472 |
910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 6 |6 P:(DE-2719)2811030 |
913 | 1 | _ | |a DE-HGF |b Gesundheit |l Neurodegenerative Diseases |1 G:(DE-HGF)POF4-350 |0 G:(DE-HGF)POF4-352 |3 G:(DE-HGF)POF4 |2 G:(DE-HGF)POF4-300 |4 G:(DE-HGF)POF |v Disease Mechanisms |x 0 |
914 | 1 | _ | |y 2023 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0200 |2 StatID |b SCOPUS |d 2020-09-11 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0300 |2 StatID |b Medline |d 2020-09-11 |
920 | 1 | _ | |0 I:(DE-2719)1710007 |k AG Kizil |l Mechanisms of Induced Plasticity of the Vertebrate Brain |x 0 |
980 | _ | _ | |a contb |
980 | _ | _ | |a VDB |
980 | _ | _ | |a I:(DE-2719)1710007 |
980 | _ | _ | |a UNRESTRICTED |
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