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EFFECTS OF ROCK INHIBITOR Y27632 AND EGFR INHIBITOR PD168393 ON HUMAN NEURAL PRECURSORS CO-CULTURED WITH RAT AUDITORY BRAINSTEM EXPLANT
Karolinska University Hospital, Sweden; Karolinska University Hospital, Sweden.
Lund University, Sweden.
Karolinska University Hospital, Sweden; Karolinska University Hospital, Sweden.
Karolinska University Hospital, Sweden; Karolinska University Hospital, Sweden; Capital Medical University, Peoples R China.
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2015 (English)In: Neuroscience, ISSN 0306-4522, E-ISSN 1873-7544, Vol. 287, 43-54 p.Article in journal (Refereed) Published
Abstract [en]

Hearing function lost by degeneration of inner ear spiral ganglion neurons (SGNs) in the auditory nervous system could potentially be compensated by cellular replacement using suitable donor cells. Donor cell-derived neuronal development with functional synaptic formation with auditory neurons of the cochlear nucleus (CN) in the brainstem is a prerequisite for a successful transplantation. Here a rat auditory brainstem explant culture system was used as a screening platform for donor cells. The explants were co-cultured with human neural precursor cells (HNPCs) to determine HNPCs developmental potential in the presence of environmental cues characteristic for the auditory brainstem region in vitro. We explored effects of pharmacological inhibition of GTPase Rho with its effector Rho-associated kinase (ROCK) and epidermal growth factor receptor (EGFR) signaling on the co-cultures. Pharmacological agents ROCK inhibitor Y27632 and EGFR blocker PD168393 were tested. Effect of the treatment on explant penetration by green fluorescent protein (GFP)-labeled HNPCs was evaluated based on the following criteria: number of GFP-HNPCs located within the explant; distance migrated by the GFP-HNPCs deep into the explant; length of the GFP+/neuronal class III beta-tubulin (TUJ1)+ processes developed and phenotypes displayed. In a short 2-week co-culture both inhibitors had growth-promoting effects on HNPCs, prominent in neurite extension elongation. Significant enhancement of migration and in-growth of HNPCs into the brain slice tissue was only observed in Y27632-treated co-cultures. Difference between Y27632- and PD168393-treated HNPCs acquiring neuronal fate was significant, though not different from the fates acquired in control co-culture. Our data suggest the presence of inhibitory mechanisms in the graft-host environment of the auditory brainstem slice co-culture system with neurite growth arresting properties which can be modulated by administration of signaling pathways antagonists. Therefore the co-culture system can be utilized for screens of donor cells and compounds regulating neuronal fate determination. (C) 2014 IBRO. Published by Elsevier Ltd. All rights reserved.

Place, publisher, year, edition, pages
PERGAMON-ELSEVIER SCIENCE LTD , 2015. Vol. 287, 43-54 p.
Keyword [en]
hearing; organotypic culture; neuronal restoration; Y27632; PD168393
National Category
Clinical Medicine
Identifiers
URN: urn:nbn:se:liu:diva-114975DOI: 10.1016/j.neuroscience.2014.12.009ISI: 000348759100006PubMedID: 25514049OAI: oai:DiVA.org:liu-114975DiVA: diva2:794134
Note

Funding Agencies|Swedish Research Council [2008-2822]; Marianne and Marcus Wallenbergs Foundation; Petrus and Augusta Hedlunds Foundation; Swedish Association of Hard of Hearing People; Acta Otolaryngologicas Foundation; Karolinska Institutet Foundations

Available from: 2015-03-10 Created: 2015-03-06 Last updated: 2017-12-04

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Olivius, Petri

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Division of Neuro and Inflammation ScienceFaculty of Medicine and Health SciencesDepartment of Otorhinolaryngology in Linköping
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