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Interleukin 15 expression in the CNS: Blockade of its activity prevents glial activation after an inflammatory injury

✍ Scribed by Diego Gómez-Nicola; Beatriz Valle-Argos; D. Wolfgang Pita-Thomas; Manuel Nieto-Sampedro


Book ID
102845692
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
823 KB
Volume
56
Category
Article
ISSN
0894-1491

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✦ Synopsis


Abstract

Although reactive glia formation after neuronal degeneration or traumatic damage is one of the hallmarks of central nervous system (CNS) injury, we have little information on the signals that direct activation of resting glia. IL‐15, a pro‐inflammatory cytokine involved in regulating the response of T and B cells, may be also key for the regulation of early inflammatory events in the nervous system. IL‐15 was expressed in the CNS, most abundantly in cerebellum and hippocampus, mainly in astrocytes and in some projection neurons. Using a rodent model of acute inflammatory injury [lipopolysaccharide (LPS) injection], we found enhanced expression of IL‐15 in both reactive astroglia and microglia, soon after CNS injury. Blockade of IL‐15 activity with an antibody to the cytokine, reversed activation of both glial types, suggesting that IL‐15 has a major role in the generation of gliotic tissue and in the regulation of neuroimmune responses. Because IL‐15 appears to modulate the inflammatory environment acutely generated after CNS injury, regulating IL‐15 expression seems a clear antiinflammatory therapy to improve the outcome of neurodegenerative diseases and CNS trauma. © 2008 Wiley‐Liss, Inc.