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- 1Institute of Anatomy and Cell Biology, Universitätsmedizin Greifswald, Greifswald, Germany
- 2The Edmond and Lily Safra Center of Brain Science, The Hebrew University of Jerusalem, Jerusalem, Israel
A commentary on
Lipocalin-2 is involved in emotional behaviors and cognitive function
by Ferreira, A. C., Pinto, V., Dá Mesquita, S., Novais, A., Sousa, J. C., Correia-Neves, M., et al. (2013). Front. Cell Neurosci. 7:122. doi: 10.3389/fncel.2013.00122
Lipocalins are a diverse family of secreted proteins that are involved in a variety of cellular processes. A member of the lipocalin protein family is lipocalin-2. Lipocalin-2 mRNA and protein expression in the adult brain, under physiological conditions, is thought to be rather low, especially in the hippocampus (Chia et al., 2011). Moreover, lipocalin-2 seems to be expressed, at least in the adult brain, by glia cells (Chia et al., 2011; Marques et al., 2012). Lipocalin-2 has been found to be upregulated in astrocytes after neuronal injury induced e.g. by kainate (Chia et al., 2011) and it has been shown that reactive astrocytes secrete lipocalin2 to promote neuron death (Bi et al., 2013).
Based on the expression of lipocalin 2 in the brain, the data shown in the paper “Lipocalin-2 is involved in emotional behaviors and cognitive function” by Ferreira and colleagues are very interesting. The data may hint a strong interplay between glia cell function and neuronal functioning. The authors demonstrate that lack of lipocalin-2 alters behavior and cognitive functions and induces morphological changes (dendritic length and spine-densities) and that absence of lipocalin-2 impairs synaptic plasticity. These interesting findings offer the opportunity to analyze the interplay of astrocytes and neurons in more detail. There are different scenarios that may account for the effects seen in the lipocalin-2 deficient mice:
(1) The observed changes may be mediated by a receptor capable of binding lipocalin, like the 24p3R (Devireddy et al., 2005), which is known to be expressed by neurons (Ip et al., 2011).
(2) Gliotransmission and the tripartite synapse (Santello et al., 2012) are known to play important roles for electrophysiological properties of neurons. Deletion of lipocalin-2 may affect the population of astrocytes, leading to changes in the activity-dependent synaptic plasticity.
(3) Deficiency for lipocalin-2 may have an effect upon embryonic brain development and/or modify other regulatory molecules, such as microRNAs whose other targets may be affected differently due to these changes.
In conclusion, lipocalin-2 regulation connects between cell types, behavioral paradigms and possibly developmental ones.
References
Bi, F., Huang, C., Tong, J., Qiu, G., Huang, B., Wu, Q., et al. (2013). Reactive astrocytes secrete lcn2 to promote neuron death. Proc. Natl. Acad. Sci. U.S.A. 110, 4069–4074. doi: 10.1073/pnas.1218497110
Chia, W. J., Dawe, G. S., and Ong, W. Y. (2011). Expression and localization of the iron-siderophore binding protein lipocalin 2 in the normal rat brain and after kainate-induced excitotoxicity. Neurochem. Int. 59, 591–599. doi: 10.1016/j.neuint.2011.04.007
Devireddy, L. R., Gazin, C., Zhu, X., and Green, M. R. (2005). A cell-surface receptor for lipocalin 24p3 selectively mediates apoptosis and iron uptake. Cell 123, 1293–1305. doi: 10.1016/j.cell.2005.10.027
Ip, J. P., Nocon, A. L., Hofer, M. J., Lim, S. L., Muller, M., and Campbell, I. L. (2011). Lipocalin 2 in the central nervous system host response to systemic lipopolysaccharide administration. J. Neuroinflammation 8:124. doi: 10.1186/1742-2094-8-124
Marques, F., Mesquita, S. D., Sousa, J. C., Coppola, G., Gao, F., Geschwind, D. H., et al. (2012). Lipocalin 2 is present in the EAE brain and is modulated by natalizumab. Front. Cell Neurosci. 6:33. doi: 10.3389/fncel.2012.00033
Keywords: lipocalin-2, astrocytes, hippocampus, synaptic plasticity, mouse
Citation: von Bohlen und Halbach O and Soreq H (2013) Hippocampal Lipocalin 2: an emotional link between neurons and glia. Front. Cell. Neurosci. 7:132. doi: 10.3389/fncel.2013.00132
Received: 02 August 2013; Accepted: 06 August 2013;
Published online: 23 August 2013.
Edited by:
Silvia Alboni, University of Modena and Reggio Emilia, ItalyCopyright © 2013 von Bohlen und Halbach and Soreq. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence:b2xpdmVyLnZvbmJvaGxlbkB1bmktZ3JlaWZzd2FsZC5kZQ==