Long term potentiation affects intracellular metalloproteinases activity in the mossy fiber ¡ª CA3 pathway
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- 作者：Grzegorz Wiera ; Tomasz W¨®jtowicz ; Katarzyna Lebida ; Aleks ; ra Piotrowska ; Dominika Drulis-Fajdasz ; Agnieszka Gomu?kiewicz ; Daria Gendosz ; Marzena Podhorska-Oko?¨®w ; Marco Capogna ; Grzegorz Wilczy¨½ski ; Piotr Dzi?giel ; Leszek Kaczmarek ; Jerzy W. Mozrzymas
- 关键词：APMA ; 4-aminophenyl mercuric acid ; CHX ; cycloheximide ; fEPSP ; field excitatory postsynaptic potential ; GFAP ; glial fibrillary acidic protein ; ISZ ; in situ zymography ; LTP ; long term potentiation ; mf-CA3 ; mossy fiber©\CA3 ; MAP-2 ; microtubule associated pr
- 刊名：Molecular and Cellular Neuroscience
- 出版年：2012
- 出版时间：June, 2012
- 年：2012
- 卷：50
- 期：2
- 页码：147-159
- 全文大小：2489 K
文摘
Matrix Metalloproteinases (MMPs) are a family of endopeptidases known to process extracellular proteins. In the last decade, studies carried out mainly on the Schaffer collateral ¡ª CA1 hippocampal projection have provided solid evidence that MMPs regulate synaptic plasticity and learning. Recently, our group has shown that MMP blockade disrupts LTP maintenance also in the mossy fiber-CA3 (mf-CA3) projection (Wojtowicz and Mozrzymas, 2010), where LTP mechanisms are profoundly different (NMDAR-independent and presynaptic expression site). However, how plasticity of this pathway correlates with activity and expression of MMPs remains unknown. Interestingly, several potential MMP substrates (especially of gelatinases) are localized intracellularly but little is known about MMP activity in this compartment. In the present study we have asked whether LTP is associated with the expression and activity of gelatinases in apparent intra- and extracellular compartments along mf-CA3 projection. In situ zymography showed that LTP induction was associated with increased gelatinases activity in the cytoplasm of the hilar and CA3 neurons. Using gelatin zymography, immunohistochemistry and immunofluorescent staining we found that this effect was due to de novo synthesis and activation of MMP-9 which, 2-3 h after LTP induction was particularly evident in the cytoplasm. In contrast, MMP-2 was localized preferentially in the nuclei and was not affected by LTP induction. In conclusion, we demonstrate that LTP induction in the mf-CA3 pathway correlates with increased expression and activity of MMP-9 and provide the first evidence that this increase is particularly evident in the neuronal cytoplasm and nucleus.