TY - JOUR
T1 - Lipocalin-2 is a chemokine inducer in the central nervous system
T2 - Role of chemokine ligand 10 (CXCL10) in lipocalin-2-induced cell migration
AU - Lee, Shinrye
AU - Kim, Jong Heon
AU - Kim, Jae Hong
AU - Seo, Jung Wan
AU - Han, Hyung Soo
AU - Lee, Won Ha
AU - Mori, Kiyoshi
AU - Nakao, Kazuwa
AU - Barasch, Jonathan
AU - Suk, Kyoungho
PY - 2011/12/23
Y1 - 2011/12/23
N2 - The secreted protein lipocalin-2 (LCN2) has been implicated in diverse cellular processes, including cell morphology and migration. Little is known, however, about the role of LCN2 in the CNS. Here, we show that LCN2 promotes cell migration through up-regulation of chemokines in brain. Studies using cultured glial cells, microvascular endothelial cells, and neuronal cells suggest that LCN2 may act as a chemokine inducer on the multiple cell types in the CNS. In particular, up-regulation of CXCL10 by JAK2/STAT3 and IKK/NF-κB pathways in astrocytes played a pivotal role in LCN2-induced cell migration. The cell migration-promoting activity of LCN2 in the CNS was verified in vivo using mouse models. The expression of LCN2 was notably increased in brain following LPS injection or focal injury. Mice lacking LCN2 showed the impaired migration of astrocytes to injury sites with a reduced CXCL10 expression in the neuroinflammation or injury models. Thus, the LCN2 proteins, secreted under inflammatory conditions, may amplify neuroinflammation by inducing CNS cells to secrete chemokines such as CXCL10, which recruit additional inflammatory cells.
AB - The secreted protein lipocalin-2 (LCN2) has been implicated in diverse cellular processes, including cell morphology and migration. Little is known, however, about the role of LCN2 in the CNS. Here, we show that LCN2 promotes cell migration through up-regulation of chemokines in brain. Studies using cultured glial cells, microvascular endothelial cells, and neuronal cells suggest that LCN2 may act as a chemokine inducer on the multiple cell types in the CNS. In particular, up-regulation of CXCL10 by JAK2/STAT3 and IKK/NF-κB pathways in astrocytes played a pivotal role in LCN2-induced cell migration. The cell migration-promoting activity of LCN2 in the CNS was verified in vivo using mouse models. The expression of LCN2 was notably increased in brain following LPS injection or focal injury. Mice lacking LCN2 showed the impaired migration of astrocytes to injury sites with a reduced CXCL10 expression in the neuroinflammation or injury models. Thus, the LCN2 proteins, secreted under inflammatory conditions, may amplify neuroinflammation by inducing CNS cells to secrete chemokines such as CXCL10, which recruit additional inflammatory cells.
UR - http://www.scopus.com/inward/record.url?scp=83755181397&partnerID=8YFLogxK
U2 - 10.1074/jbc.M111.299248
DO - 10.1074/jbc.M111.299248
M3 - Article
C2 - 22030398
AN - SCOPUS:83755181397
SN - 0021-9258
VL - 286
SP - 43855
EP - 43870
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 51
ER -