Glial Cell Line-Derived Neurotrophic Factor Induces Barrier Function of Endothelial Cells Forming the Blood–Brain Barrier

Since a deep involvement of astrocytes, a kind of glial cells, in differentiation of the blood–brain barrier (BBB) has been suggested, we examined the relation of glial cell line-derived neurotrophic factor (GDNF) to the BBB. First, immunohistochemical examination of the cerebral cortex of rats reve...

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Published inBiochemical and biophysical research communications Vol. 261; no. 1; pp. 108 - 112
Main Authors Igarashi, Yo, Utsumi, Hiroyuki, Chiba, Hideki, Yamada-Sasamori, Yumiko, Tobioka, Hirotoshi, Kamimura, Yasuhiro, Furuuchi, Ken, Kokai, Yasuo, Nakagawa, Takashi, Mori, Michio, Sawada, Norimasa
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 22.07.1999
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Abstract Since a deep involvement of astrocytes, a kind of glial cells, in differentiation of the blood–brain barrier (BBB) has been suggested, we examined the relation of glial cell line-derived neurotrophic factor (GDNF) to the BBB. First, immunohistochemical examination of the cerebral cortex of rats revealed that glial cell line-derived neurotrophic factor receptor (GFRα1) was preferentially expressed on the cell membranes of capillary endothelial cells. Second, to elucidate the effects of GDNF on the BBB, capillary endothelial cells isolated from the porcine cerebral cortex were cultured and then changes in tight junction function of the endothelial cells were examined after addition of GDNF, in terms of transendothelial electrical resistance (TER) and permeability. GDNF at concentrations of 0.1 and 1 ng/ml significantly activated the barrier function of the endothelial cells in the presence of cAMP. Since GDNF is secreted from astrocytes sheathing capillary endothelial cells in the brain cortex, our results strongly suggest that GDNF enhances the barrier function of tight junctions of the BBB on the one hand, and also supports the survival of neurons on the other hand.
AbstractList Since a deep involvement of astrocytes, a kind of glial cells, in differentiation of the blood-brain barrier (BBB) has been suggested, we examined the relation of glial cell line-derived neurotrophic factor (GDNF) to the BBB. First, immunohistochemical examination of the cerebral cortex of rats revealed that glial cell line-derived neurotrophic factor receptor (GFRalpha1) was preferentially expressed on the cell membranes of capillary endothelial cells. Second, to elucidate the effects of GDNF on the BBB, capillary endothelial cells isolated from the porcine cerebral cortex were cultured and then changes in tight junction function of the endothelial cells were examined after addition of GDNF, in terms of transendothelial electrical resistance (TER) and permeability. GDNF at concentrations of 0.1 and 1 ng/ml significantly activated the barrier function of the endothelial cells in the presence of cAMP. Since GDNF is secreted from astrocytes sheathing capillary endothelial cells in the brain cortex, our results strongly suggest that GDNF enhances the barrier function of tight junctions of the BBB on the one hand, and also supports the survival of neurons on the other hand.Since a deep involvement of astrocytes, a kind of glial cells, in differentiation of the blood-brain barrier (BBB) has been suggested, we examined the relation of glial cell line-derived neurotrophic factor (GDNF) to the BBB. First, immunohistochemical examination of the cerebral cortex of rats revealed that glial cell line-derived neurotrophic factor receptor (GFRalpha1) was preferentially expressed on the cell membranes of capillary endothelial cells. Second, to elucidate the effects of GDNF on the BBB, capillary endothelial cells isolated from the porcine cerebral cortex were cultured and then changes in tight junction function of the endothelial cells were examined after addition of GDNF, in terms of transendothelial electrical resistance (TER) and permeability. GDNF at concentrations of 0.1 and 1 ng/ml significantly activated the barrier function of the endothelial cells in the presence of cAMP. Since GDNF is secreted from astrocytes sheathing capillary endothelial cells in the brain cortex, our results strongly suggest that GDNF enhances the barrier function of tight junctions of the BBB on the one hand, and also supports the survival of neurons on the other hand.
Since a deep involvement of astrocytes, a kind of glial cells, in differentiation of the blood-brain barrier (BBB) has been suggested, we examined the relation of glial cell line-derived neurotrophic factor (GDNF) to the BBB. First, immunohistochemical examination of the cerebral cortex of rats revealed that glial cell line-derived neurotrophic factor receptor (GFRalpha1) was preferentially expressed on the cell membranes of capillary endothelial cells. Second, to elucidate the effects of GDNF on the BBB, capillary endothelial cells isolated from the porcine cerebral cortex were cultured and then changes in tight junction function of the endothelial cells were examined after addition of GDNF, in terms of transendothelial electrical resistance (TER) and permeability. GDNF at concentrations of 0.1 and 1 ng/ml significantly activated the barrier function of the endothelial cells in the presence of cAMP. Since GDNF is secreted from astrocytes sheathing capillary endothelial cells in the brain cortex, our results strongly suggest that GDNF enhances the barrier function of tight junctions of the BBB on the one hand, and also supports the survival of neurons on the other hand.
Since a deep involvement of astrocytes, a kind of glial cells, in differentiation of the blood-brain barrier (BBB) has been suggested, we examined the relation of glial cell line-derived neurotrophic factor (GDNF) to the BBB. First, immunohistochemical examination of the cerebral cortex of rats revealed that glial cell line-derived neurotrophic factor receptor (GFR alpha 1) was preferentially expressed on the cell membranes of capillary endothelial cells. Second, to elucidate the effects of GDNF on the BBB, capillary endothelial cells isolated from the porcine cerebral cortex were cultured and then changes in tight junction function of the endothelial cells were examined after addition of GDNF, in terms of transendothelial electrical resistance (TER) and permeability. GDNF at concentrations of 0.1 and 1 ng/ml significantly activated the barrier function of the endothelial cells in the presence of cAMP. Since GDNF is secreted from astrocytes sheathing capillary endothelial cells in the brain cortex, our results strongly suggest that GDNF enhances the barrier function of tight junctions of the BBB on the one hand, and also supports the survival of neurons on the other hand.
Since a deep involvement of astrocytes, a kind of glial cells, in differentiation of the blood–brain barrier (BBB) has been suggested, we examined the relation of glial cell line-derived neurotrophic factor (GDNF) to the BBB. First, immunohistochemical examination of the cerebral cortex of rats revealed that glial cell line-derived neurotrophic factor receptor (GFRα1) was preferentially expressed on the cell membranes of capillary endothelial cells. Second, to elucidate the effects of GDNF on the BBB, capillary endothelial cells isolated from the porcine cerebral cortex were cultured and then changes in tight junction function of the endothelial cells were examined after addition of GDNF, in terms of transendothelial electrical resistance (TER) and permeability. GDNF at concentrations of 0.1 and 1 ng/ml significantly activated the barrier function of the endothelial cells in the presence of cAMP. Since GDNF is secreted from astrocytes sheathing capillary endothelial cells in the brain cortex, our results strongly suggest that GDNF enhances the barrier function of tight junctions of the BBB on the one hand, and also supports the survival of neurons on the other hand.
Author Igarashi, Yo
Mori, Michio
Tobioka, Hirotoshi
Kokai, Yasuo
Utsumi, Hiroyuki
Furuuchi, Ken
Chiba, Hideki
Nakagawa, Takashi
Sawada, Norimasa
Kamimura, Yasuhiro
Yamada-Sasamori, Yumiko
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  surname: Igarashi
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  organization: Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060, Japan
– sequence: 2
  givenname: Hiroyuki
  surname: Utsumi
  fullname: Utsumi, Hiroyuki
  organization: Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060, Japan
– sequence: 3
  givenname: Hideki
  surname: Chiba
  fullname: Chiba, Hideki
  organization: Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060, Japan
– sequence: 4
  givenname: Yumiko
  surname: Yamada-Sasamori
  fullname: Yamada-Sasamori, Yumiko
  organization: Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060, Japan
– sequence: 5
  givenname: Hirotoshi
  surname: Tobioka
  fullname: Tobioka, Hirotoshi
  organization: Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060, Japan
– sequence: 6
  givenname: Yasuhiro
  surname: Kamimura
  fullname: Kamimura, Yasuhiro
  organization: Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060, Japan
– sequence: 7
  givenname: Ken
  surname: Furuuchi
  fullname: Furuuchi, Ken
  organization: Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060, Japan
– sequence: 8
  givenname: Yasuo
  surname: Kokai
  fullname: Kokai, Yasuo
  organization: Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060, Japan
– sequence: 9
  givenname: Takashi
  surname: Nakagawa
  fullname: Nakagawa, Takashi
  organization: Department of Neurosurgery, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060, Japan
– sequence: 10
  givenname: Michio
  surname: Mori
  fullname: Mori, Michio
  organization: Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060, Japan
– sequence: 11
  givenname: Norimasa
  surname: Sawada
  fullname: Sawada, Norimasa
  organization: Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060, Japan
BackLink https://www.ncbi.nlm.nih.gov/pubmed/10405331$$D View this record in MEDLINE/PubMed
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Snippet Since a deep involvement of astrocytes, a kind of glial cells, in differentiation of the blood–brain barrier (BBB) has been suggested, we examined the relation...
Since a deep involvement of astrocytes, a kind of glial cells, in differentiation of the blood-brain barrier (BBB) has been suggested, we examined the relation...
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SubjectTerms Animals
Blood-Brain Barrier - drug effects
Cell Membrane - chemistry
Cell Membrane - drug effects
Cell Membrane Permeability - drug effects
Cells, Cultured
Cerebral Cortex - blood supply
Cerebral Cortex - chemistry
Cerebral Cortex - cytology
Cyclic AMP - pharmacology
Dose-Response Relationship, Drug
Drosophila Proteins
Electric Impedance
Endothelium, Vascular - chemistry
Endothelium, Vascular - cytology
Endothelium, Vascular - drug effects
Endothelium, Vascular - physiology
Glial Cell Line-Derived Neurotrophic Factor
Glial Cell Line-Derived Neurotrophic Factor Receptors
Immunohistochemistry
Nerve Growth Factors
Nerve Tissue Proteins - pharmacology
Proto-Oncogene Proteins - analysis
Proto-Oncogene Proteins c-ret
Rats
Receptor Protein-Tyrosine Kinases - analysis
Swine
Tight Junctions - drug effects
Tight Junctions - physiology
Time Factors
Title Glial Cell Line-Derived Neurotrophic Factor Induces Barrier Function of Endothelial Cells Forming the Blood–Brain Barrier
URI https://dx.doi.org/10.1006/bbrc.1999.0992
https://www.ncbi.nlm.nih.gov/pubmed/10405331
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