Modulation of Glial and Neuronal Migration by Lipocalin-2 in Zebrafish.
- Author:
Ho KIM
1
;
Shinrye LEE
;
Hae Chul PARK
;
Won Ha LEE
;
Myung Shik LEE
;
Kyoungho SUK
Author Information
- Publication Type:Original Article ; In Vitro
- Keywords: LCN2; Glia; Cell migration; Neuroinflammation; Central nervous system; Spinal cord
- MeSH: Astrocytes; Cell Movement; Central Nervous System; Culture Media, Conditioned; Embryonic Structures; Microglia; Neuroglia; Neurons; Proteins; Spinal Cord; Zebrafish
- From:Immune Network 2011;11(6):342-347
- CountryRepublic of Korea
- Language:English
- Abstract: BACKGROUND: Glial cells are involved in immune and inflammatory responses in the central nervous system (CNS). Glial cells such as microglia and astrocytes also provide structural and functional support for neurons. Migration and morphological changes of CNS cells are associated with their physiological as well as pathological functions. The secreted protein lipocalin-2 (LCN2) has been previously implicated in regulation of diverse cellular processes of glia and neurons, including cell migration and morphology. METHODS: Here, we employed a zebrafish model to analyze the role of LCN2 in CNS cell migration and morphology in vivo. In the first part of this study, we examined the indirect effect of LCN2 on cell migration and morphology of microglia, astrocytes, and neurons cultured in vitro. RESULTS: Conditioned media collected from LCN2-treated astrocytes augmented migration of glia and neurons in the Boyden chamber assay. The conditioned media also increased the number of neuronal processes. Next, in order to further understand the role of LCN2 in the CNS in vivo, LCN2 was ectopically expressed in the zebrafish spinal cord. Expression of exogenous LCN2 modulated neuronal cell migration in the spinal cord of zebrafish embryos, supporting the role of LCN2 as a cell migration regulator in the CNS. CONCLUSION: Thus, LCN2 proteins secreted under diverse conditions may play an important role in CNS immune and inflammatory responses by controlling cell migration and morphology.
