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Activity-dependent long-term plasticity of afferent synapses on grafted stem/progenitor cell-derived neurons.

Toft Sörensen, Andreas LU ; Rogelius, Nina LU ; Lundberg, Cecilia LU orcid and Kokaia, Merab LU (2011) In Experimental Neurology 229. p.274-281
Abstract
Stem cell-based cell replacement therapies aiming at restoring injured or diseased brain function ultimately rely on the capability of transplanted cells to promote functional recovery. The mechanisms by which stem cell-based therapies for neurological conditions can lead to functional recovery are uncertain, but structural and functional repair appears to depend on integration of transplanted cell-derived neurons into neuronal circuitries. The nature by which stem/progenitor cell-derived neurons synaptically integrate into neuronal circuitries is largely unexplored. Here we show that transplanted GFP-labeled neuronal progenitor cells into the rat hippocampus exhibit mature neuronal morphology following 4-10 weeks. GFP-positive cells were... (More)
Stem cell-based cell replacement therapies aiming at restoring injured or diseased brain function ultimately rely on the capability of transplanted cells to promote functional recovery. The mechanisms by which stem cell-based therapies for neurological conditions can lead to functional recovery are uncertain, but structural and functional repair appears to depend on integration of transplanted cell-derived neurons into neuronal circuitries. The nature by which stem/progenitor cell-derived neurons synaptically integrate into neuronal circuitries is largely unexplored. Here we show that transplanted GFP-labeled neuronal progenitor cells into the rat hippocampus exhibit mature neuronal morphology following 4-10 weeks. GFP-positive cells were preferentially integrated into the principal cell layers of hippocampus, particularly CA3. Patch-clamp recordings from GFP-expressing cells revealed that they generated fast action potentials, and their intrinsic membrane properties were overall similar to endogenous host neurons recorded in same areas. As judged by occurrence of spontaneous excitatory postsynaptic currents (EPSCs), transplanted GFP-positive cells were synaptically integrated into the host circuitry. Comparable to host neurons, both paired-pulse depression and facilitation of afferent fiber stimulation-evoked EPSCs were observed in GFP-positive cells. Upon high-frequency stimulation, GFP-positive cells displayed post-tetanic potentiation of EPSCs, in some cases followed by long-term potentiation (LTP) lasting for more than 30 min. Our data show for the first time that transplanted neuronal progenitor cells can become functional neurons and their afferent synapses are capable of expressing activity-dependent short and long-term plasticity. These synaptic properties may facilitate host-to-graft interactions and regulate activity of the grafted cells promoting functional recovery of the diseased brain. (Less)
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author
; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Experimental Neurology
volume
229
pages
274 - 281
publisher
Elsevier
external identifiers
  • wos:000291419400011
  • pmid:21324317
  • scopus:79956138622
  • pmid:21324317
ISSN
0014-4886
DOI
10.1016/j.expneurol.2011.02.008
language
English
LU publication?
yes
id
e8152daf-3cb2-4ab0-abcc-09a0fced2eae (old id 1831783)
alternative location
http://www.ncbi.nlm.nih.gov/pubmed/21324317?dopt=Abstract
date added to LUP
2016-04-01 11:16:11
date last changed
2022-01-26 06:41:16
@article{e8152daf-3cb2-4ab0-abcc-09a0fced2eae,
  abstract     = {{Stem cell-based cell replacement therapies aiming at restoring injured or diseased brain function ultimately rely on the capability of transplanted cells to promote functional recovery. The mechanisms by which stem cell-based therapies for neurological conditions can lead to functional recovery are uncertain, but structural and functional repair appears to depend on integration of transplanted cell-derived neurons into neuronal circuitries. The nature by which stem/progenitor cell-derived neurons synaptically integrate into neuronal circuitries is largely unexplored. Here we show that transplanted GFP-labeled neuronal progenitor cells into the rat hippocampus exhibit mature neuronal morphology following 4-10 weeks. GFP-positive cells were preferentially integrated into the principal cell layers of hippocampus, particularly CA3. Patch-clamp recordings from GFP-expressing cells revealed that they generated fast action potentials, and their intrinsic membrane properties were overall similar to endogenous host neurons recorded in same areas. As judged by occurrence of spontaneous excitatory postsynaptic currents (EPSCs), transplanted GFP-positive cells were synaptically integrated into the host circuitry. Comparable to host neurons, both paired-pulse depression and facilitation of afferent fiber stimulation-evoked EPSCs were observed in GFP-positive cells. Upon high-frequency stimulation, GFP-positive cells displayed post-tetanic potentiation of EPSCs, in some cases followed by long-term potentiation (LTP) lasting for more than 30 min. Our data show for the first time that transplanted neuronal progenitor cells can become functional neurons and their afferent synapses are capable of expressing activity-dependent short and long-term plasticity. These synaptic properties may facilitate host-to-graft interactions and regulate activity of the grafted cells promoting functional recovery of the diseased brain.}},
  author       = {{Toft Sörensen, Andreas and Rogelius, Nina and Lundberg, Cecilia and Kokaia, Merab}},
  issn         = {{0014-4886}},
  language     = {{eng}},
  pages        = {{274--281}},
  publisher    = {{Elsevier}},
  series       = {{Experimental Neurology}},
  title        = {{Activity-dependent long-term plasticity of afferent synapses on grafted stem/progenitor cell-derived neurons.}},
  url          = {{https://lup.lub.lu.se/search/files/2522264/1852395.pdf}},
  doi          = {{10.1016/j.expneurol.2011.02.008}},
  volume       = {{229}},
  year         = {{2011}},
}