toggle visibility Search & Display Options

Select All    Deselect All
 |   | 
  Record Links
Author (up) Pamies, D.; Barreras, P.; Block, K.; Makri, G.; Kumar, A.; Wiersma, D.; Smirnova, L.; Zhang, C.; Bressler, J.; Christian, K.M.; Harris, G.; Ming, G.-L.; Berlinicke, C.J.; Kyro, K.; Song, H.; Pardo, C.A.; Hartung, T.; Hogberg, H.T. url  doi
  Title A human brain microphysiological system derived from induced pluripotent stem cells to study neurological diseases and toxicity Type Journal Article
  Year 2016 Publication Altex Abbreviated Journal Altex  
  Volume Issue Pages  
  Keywords 3D culture; Cns; brain; microphysiological system; myelination  
  Abstract Human in-vitro models of brain neurophysiology are needed to investigate molecular and cellular mechanisms associated with neurological disorders and neurotoxicity. We have developed a reproducible iPSC-derived human 3D brain microphysiological system (BMPS), comprised of differentiated mature neurons and glial cells (astrocytes and oligodendrocytes) that reproduce neuronal-glial interactions and connectivity. BMPS mature over eight weeks and show the critical elements of neuronal function: synaptogenesis and neuron-to-neuron (e.g. spontaneous electric field potentials) and neuronal-glial interactions (e.g. myelination), that mimic the microenvironment of the central nervous system, rarely seen in vitro so far. The BMPS shows 40% overall myelination after 8 weeks of differentiation. Myelin was observed by immunohistochemistry and confirmed by confocal microscopy 3D reconstruction and electron microscopy. These findings are of particular relevance since myelin is crucial for proper neuronal function and development. The ability to assess oligodendroglia function and mechanisms associated with myelination in this BMPS model provide an excellent tool for future studies of neurological disorders such as multiple sclerosis and other demyelinating diseases. Thus, the BMPS provides a suitable and reliable model to investigate neuron-neuroglia function in neurotoxicology or other pathogenic mechanisms.  
  Address Center for Alternatives to Animal Testing, Johns Hopkins University, Baltimore, USA  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 1868-596X ISBN Medium  
  Area Expedition Conference  
  Notes PMID:27883356 Approved no  
  Call Number ref @ user @ Serial 95911  
Permanent link to this record
Select All    Deselect All
 |   | 

Save Citations:
Export Records: