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bFGF and EGF modulate trauma-induced proliferation and neurogenesis in juvenile organotypic hippocampal slice cultures

bFGF and EGF modulate trauma-induced proliferation and neurogenesis in juvenile organotypic hippocampal slice cultures
bFGF and EGF modulate trauma-induced proliferation and neurogenesis in juvenile organotypic hippocampal slice cultures
Since postnatal and adult mammalian brains have been shown to retain an ability to generate neurons from endogenous stem cells throughout life, these cells could play a central role in regeneration after neuronal loss. Therefore, we studied cell proliferation, glio- and neurogenesis respectively after brain injury in organotypic hippocampal slice cultures using a focal trauma by transecting Schaffer collaterals in the cornu ammonis (CA) 2 region mechanically. After determination of cell death using propidium iodide, neuroregenerative processes were quantitatively analyzed by various immunohistochemical techniques at different time points post injury. As this endogenous insult-induced neurogenesis is rather inefficient, we investigated if it can be enhanced by application of exogenous growth factors.
Exogenous basic fibroblast growth factor (bFGF) enhanced neurogenesis significantly in the dentate gyrus (DG) region. A neutralizing antibody against endogenous bFGF revealed a significant decrease of basal and trauma-induced proliferation. Reverse transcription polymerase chain reaction (RT-PCR) studies exhibited a downregulation of FGF messenger ribonucleic acid (mRNA) transcription after the antibody treatment. In contrast, epidermal growth factor (EGF) increased proliferation, but not neurogenesis. A combination of bFGF and EGF displayed an EGF-like effect on proliferation and no effect on neurogenesis. These results demonstrate, that in our model bFGF but not EGF sustains neurogenesis, whereas together the two growth factors permit an increased proliferation but not neurogenesis in organic hippocampal slice cultures.
stem cells, growth factors, endogenous repair, in vitro, regeneration, degeneration
0006-8993
78-89
Laskowski, Alexandra
f06f47d0-8587-4074-91b6-eb59f28572ae
Schmidt, Werner
72a5867a-1a24-4d76-9bbc-c179f115bb2d
Dinkel, Klaus
76cfe276-d6b7-440f-9b4b-e29f6d3ba125
Martinez-Sanchez, Monica
8e06f214-ff8b-4e22-970b-47005fede5ef
Reymann, Klaus G.
be5a8cb9-cc02-42d7-a00a-3e3aa6bf3850
Laskowski, Alexandra
f06f47d0-8587-4074-91b6-eb59f28572ae
Schmidt, Werner
72a5867a-1a24-4d76-9bbc-c179f115bb2d
Dinkel, Klaus
76cfe276-d6b7-440f-9b4b-e29f6d3ba125
Martinez-Sanchez, Monica
8e06f214-ff8b-4e22-970b-47005fede5ef
Reymann, Klaus G.
be5a8cb9-cc02-42d7-a00a-3e3aa6bf3850

Laskowski, Alexandra, Schmidt, Werner, Dinkel, Klaus, Martinez-Sanchez, Monica and Reymann, Klaus G. (2005) bFGF and EGF modulate trauma-induced proliferation and neurogenesis in juvenile organotypic hippocampal slice cultures. Brain Research, 1037 (1-2), 78-89. (doi:10.1016/j.brainres.2004.12.035).

Record type: Article

Abstract

Since postnatal and adult mammalian brains have been shown to retain an ability to generate neurons from endogenous stem cells throughout life, these cells could play a central role in regeneration after neuronal loss. Therefore, we studied cell proliferation, glio- and neurogenesis respectively after brain injury in organotypic hippocampal slice cultures using a focal trauma by transecting Schaffer collaterals in the cornu ammonis (CA) 2 region mechanically. After determination of cell death using propidium iodide, neuroregenerative processes were quantitatively analyzed by various immunohistochemical techniques at different time points post injury. As this endogenous insult-induced neurogenesis is rather inefficient, we investigated if it can be enhanced by application of exogenous growth factors.
Exogenous basic fibroblast growth factor (bFGF) enhanced neurogenesis significantly in the dentate gyrus (DG) region. A neutralizing antibody against endogenous bFGF revealed a significant decrease of basal and trauma-induced proliferation. Reverse transcription polymerase chain reaction (RT-PCR) studies exhibited a downregulation of FGF messenger ribonucleic acid (mRNA) transcription after the antibody treatment. In contrast, epidermal growth factor (EGF) increased proliferation, but not neurogenesis. A combination of bFGF and EGF displayed an EGF-like effect on proliferation and no effect on neurogenesis. These results demonstrate, that in our model bFGF but not EGF sustains neurogenesis, whereas together the two growth factors permit an increased proliferation but not neurogenesis in organic hippocampal slice cultures.

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More information

Published date: 2005
Keywords: stem cells, growth factors, endogenous repair, in vitro, regeneration, degeneration

Identifiers

Local EPrints ID: 27634
URI: http://eprints.soton.ac.uk/id/eprint/27634
ISSN: 0006-8993
PURE UUID: 184cacaa-3772-43ca-a7fe-1183397564f4

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Date deposited: 27 Apr 2006
Last modified: 15 Mar 2024 07:20

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Contributors

Author: Alexandra Laskowski
Author: Werner Schmidt
Author: Klaus Dinkel
Author: Monica Martinez-Sanchez
Author: Klaus G. Reymann

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