TY - JOUR
T1 - Brain injury and tumor necrosis factors induce calbindin D‐28K in astrocytes
T2 - Evidence for a cytoprotective response
AU - Mattson, M. P.
AU - Cheng, B.
AU - Baldwin, S. A.
AU - Smith‐Swintosky, V. L.
AU - Keller, J.
AU - Geddes, J. W.
AU - Scheff, S. W.
AU - Christakos, S.
PY - 1995/10/15
Y1 - 1995/10/15
N2 - Calbindin is a 28 kDa calcium‐binding protein expressed in restricted neuronal populations in the mammalian brain where it may play a role in protecting neurons against excitotoxic insults. Recent findings indicate that electrical activity and some neurotrophic factors can induce the expression of calbindin in neurons. We now report that brain injury, effected by systemic administration of the excitotoxin kainate or mechanical trauma, induces expression of calbindin in cells of the corpus callosum and subcortical white matter. Immunohistochemical analysis using antibodies to the astrocyte‐specific proteins (glial fibrillary acidic protein and S‐100β) established the identity of calbindin immunoreactive cells as astrocytes. Because brain injury is known to induce the expression of several neurotrophic factors and cytokines, we employed cultures of hippocampal and neocortical astrocytes to test the hypothesis that such factors can induce expression of calbindin in astrocytes. Tumor necrosis factors (TNFβ and TNFβ), cytokines that are expressed in response to brain injury, induced the expression of calbindin in cultured rat hippocampal and neocortical astrocytes. Two neurotrophic factors, basic fibroblast growth factor and nerve growth factor, did not induce calbindin in astrocytes. TNF‐treated, calbindin‐expressing astrocytes were resistant to acidosis and calcium ionophore toxicity, suggesting that TNFs and calbindin may serve a cytoprotective role in astrocytes in the injured brain. © 1995 Wiley‐Liss, Inc.
AB - Calbindin is a 28 kDa calcium‐binding protein expressed in restricted neuronal populations in the mammalian brain where it may play a role in protecting neurons against excitotoxic insults. Recent findings indicate that electrical activity and some neurotrophic factors can induce the expression of calbindin in neurons. We now report that brain injury, effected by systemic administration of the excitotoxin kainate or mechanical trauma, induces expression of calbindin in cells of the corpus callosum and subcortical white matter. Immunohistochemical analysis using antibodies to the astrocyte‐specific proteins (glial fibrillary acidic protein and S‐100β) established the identity of calbindin immunoreactive cells as astrocytes. Because brain injury is known to induce the expression of several neurotrophic factors and cytokines, we employed cultures of hippocampal and neocortical astrocytes to test the hypothesis that such factors can induce expression of calbindin in astrocytes. Tumor necrosis factors (TNFβ and TNFβ), cytokines that are expressed in response to brain injury, induced the expression of calbindin in cultured rat hippocampal and neocortical astrocytes. Two neurotrophic factors, basic fibroblast growth factor and nerve growth factor, did not induce calbindin in astrocytes. TNF‐treated, calbindin‐expressing astrocytes were resistant to acidosis and calcium ionophore toxicity, suggesting that TNFs and calbindin may serve a cytoprotective role in astrocytes in the injured brain. © 1995 Wiley‐Liss, Inc.
KW - acidosis
KW - calcium‐binding protein
KW - corpus callosum
KW - cytokine
KW - excitotoxicity
KW - fura‐2
KW - hippocampus
KW - kainate
KW - nerve growth factor
KW - traumatic brain injury
UR - http://www.scopus.com/inward/record.url?scp=0028845422&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0028845422&partnerID=8YFLogxK
U2 - 10.1002/jnr.490420310
DO - 10.1002/jnr.490420310
M3 - Article
C2 - 8583504
AN - SCOPUS:0028845422
SN - 0360-4012
VL - 42
SP - 357
EP - 370
JO - Journal of Neuroscience Research
JF - Journal of Neuroscience Research
IS - 3
ER -