Premium
IL‐1 β increases intracellular calcium through an IL‐1 type 1 receptor mediated mechanism in C6 astrocytic cells
Author(s) -
Pita Ignacio,
Jelaso Anna M.,
Ide Charles F.
Publication year - 1999
Publication title -
international journal of developmental neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.761
H-Index - 88
eISSN - 1873-474X
pISSN - 0736-5748
DOI - 10.1016/s0736-5748(99)00063-5
Subject(s) - mechanism (biology) , intracellular , calcium in biology , microbiology and biotechnology , chemistry , receptor , neuroscience , biology , biophysics , biochemistry , physics , quantum mechanics
Interleukin‐1β (IL‐1β) is a cytokine that regulates a variety of biological processes. In addition to its traditional role in the immune system, IL‐1β plays an integral role in neural‐immune and developmental processes in the nervous system. The pleiotropic ability of IL‐1β may be due to the activation of different signal transduction mechanisms in specific cell types or under certain cellular conditions. We have previously demonstrated that IL‐1β regulates healing and repair in the developing, mammalian nervous system. In the damaged perinatal mouse brain, IL‐1β is expressed in astrocytes that change from a stellate to a spindle‐shaped morphology. The spindle‐shaped astrocytes enclose the wound, separating the healthy from damaged neural tissue. The shape change and subsequent repair processes are IL‐1β activity‐dependent, acting through the IL‐1 type 1 receptor (IL‐1R1), as co‐application of the IL‐1type 1 receptor antagonist protein (IL‐1ra) blocks IL‐1β induced effects. In the C6 astrocytic cell line, IL‐1β induced similar shape changes and upregulated expression of the cytoskeletal protein, glial fibrillary acidic protein (GFAP). Since cytoskeletal changes, as well as specific signal transduction mechanisms, are associated with increases in intracellular calcium ([Ca 2+ ] i ), studies were carried out to determine if increases in [Ca 2+ ] i induced by IL‐1β occurred through activation of the IL‐1R1 in C6 cells. Cells were treated with IL‐1β and/or IL‐1ra, followed by measurement of relative changes in [Ca 2+ ] i using fura‐2 fluorescence imaging methods. IL‐1β increased [Ca 2+ ] i levels in a dose and time dependent manner. Treatment with IL‐1ra blocked IL‐1β induced increases in [Ca 2+ ] i , indicating that IL‐1β acts through the IL‐1R1. Immunocytochemistry experiments showed that untreated C6 cells normally express IL‐1β, IL‐1ra, and IL‐1R1. Thus, IL‐1 system molecules may play a role in normal C6 astrocyte physiology.