In vitro differences between astrocytes of control and Wobbler mice spinal cord

The Wobbler mouse, a model of amyotrophic lateral sclerosis (ALS), presents motorneuron degeneration and pronounced astrogliosis in the spinal cord. We have studied factors controlling astrocyte proliferation in cultures derived from Wobbler and control mice spinal cord. Basal rate of [3H]thymidine...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado: 1999
Materias:
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03643190_v24_n12_p1535_GonzalezDeniselle
http://hdl.handle.net/20.500.12110/paper_03643190_v24_n12_p1535_GonzalezDeniselle
Aporte de:
id paper:paper_03643190_v24_n12_p1535_GonzalezDeniselle
record_format dspace
spelling paper:paper_03643190_v24_n12_p1535_GonzalezDeniselle2023-06-08T15:35:34Z In vitro differences between astrocytes of control and Wobbler mice spinal cord Astrocytes Culture Glial fibrillary acidic protein Glucocorticoids Interleukin 1 TGF-β1 Wobbler mouse corticosterone glial fibrillary acidic protein interleukin 1alpha transforming growth factor beta1 amyotrophic lateral sclerosis animal cell article astrocyte astrocytosis cell proliferation controlled study female male motoneuron mouse nerve cell degeneration nonhuman priority journal protein expression spinal cord atrophy Animals Astrocytes Cell Division Cells, Cultured Corticosterone Female Glial Fibrillary Acidic Protein Gliosis Interleukin-1 Kinetics Male Mice Mice, Inbred Strains Mice, Neurologic Mutants Motor Neuron Disease Neuroprotective Agents Pregnatrienes Receptors, Glucocorticoid Reference Values Spinal Cord Thymidine Transforming Growth Factor beta Animalia The Wobbler mouse, a model of amyotrophic lateral sclerosis (ALS), presents motorneuron degeneration and pronounced astrogliosis in the spinal cord. We have studied factors controlling astrocyte proliferation in cultures derived from Wobbler and control mice spinal cord. Basal rate of [3H]thymidine incorporation was 15 times lower in Wobbler astrocytes. While in control cultured cells interleukin-1α (IL-1) and corticosterone (CORT) significantly increased proliferation, both agents were inactive in Wobbler astrocytes. The lack of response to CORT was not due to the absence of glucocorticoid receptors, because similar receptor amounts were found in Wobbler and control astrocytes. In contrast to IL-1 and CORT, transforming growth factor-β1 (TGF-β1) substantially increased proliferation of Wobbler astrocytes but not of control cells. Differences in response to TGF- β1 were also obtained by measuring glial fibrillary acidic protein (GFAP) immunoreaction intensity, which was substantially higher in Wobbler astrocytes. Thus, abnormal responses to different mitogens characterized Wobbler astrocytes in culture. We suggest that TGF-β1 may play a role in the reactive gliosis and GFAP hyperexpression found in the degenerating spinal cord of this model of ALS. 1999 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03643190_v24_n12_p1535_GonzalezDeniselle http://hdl.handle.net/20.500.12110/paper_03643190_v24_n12_p1535_GonzalezDeniselle
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Astrocytes
Culture
Glial fibrillary acidic protein
Glucocorticoids
Interleukin 1
TGF-β1
Wobbler mouse
corticosterone
glial fibrillary acidic protein
interleukin 1alpha
transforming growth factor beta1
amyotrophic lateral sclerosis
animal cell
article
astrocyte
astrocytosis
cell proliferation
controlled study
female
male
motoneuron
mouse
nerve cell degeneration
nonhuman
priority journal
protein expression
spinal cord atrophy
Animals
Astrocytes
Cell Division
Cells, Cultured
Corticosterone
Female
Glial Fibrillary Acidic Protein
Gliosis
Interleukin-1
Kinetics
Male
Mice
Mice, Inbred Strains
Mice, Neurologic Mutants
Motor Neuron Disease
Neuroprotective Agents
Pregnatrienes
Receptors, Glucocorticoid
Reference Values
Spinal Cord
Thymidine
Transforming Growth Factor beta
Animalia
spellingShingle Astrocytes
Culture
Glial fibrillary acidic protein
Glucocorticoids
Interleukin 1
TGF-β1
Wobbler mouse
corticosterone
glial fibrillary acidic protein
interleukin 1alpha
transforming growth factor beta1
amyotrophic lateral sclerosis
animal cell
article
astrocyte
astrocytosis
cell proliferation
controlled study
female
male
motoneuron
mouse
nerve cell degeneration
nonhuman
priority journal
protein expression
spinal cord atrophy
Animals
Astrocytes
Cell Division
Cells, Cultured
Corticosterone
Female
Glial Fibrillary Acidic Protein
Gliosis
Interleukin-1
Kinetics
Male
Mice
Mice, Inbred Strains
Mice, Neurologic Mutants
Motor Neuron Disease
Neuroprotective Agents
Pregnatrienes
Receptors, Glucocorticoid
Reference Values
Spinal Cord
Thymidine
Transforming Growth Factor beta
Animalia
In vitro differences between astrocytes of control and Wobbler mice spinal cord
topic_facet Astrocytes
Culture
Glial fibrillary acidic protein
Glucocorticoids
Interleukin 1
TGF-β1
Wobbler mouse
corticosterone
glial fibrillary acidic protein
interleukin 1alpha
transforming growth factor beta1
amyotrophic lateral sclerosis
animal cell
article
astrocyte
astrocytosis
cell proliferation
controlled study
female
male
motoneuron
mouse
nerve cell degeneration
nonhuman
priority journal
protein expression
spinal cord atrophy
Animals
Astrocytes
Cell Division
Cells, Cultured
Corticosterone
Female
Glial Fibrillary Acidic Protein
Gliosis
Interleukin-1
Kinetics
Male
Mice
Mice, Inbred Strains
Mice, Neurologic Mutants
Motor Neuron Disease
Neuroprotective Agents
Pregnatrienes
Receptors, Glucocorticoid
Reference Values
Spinal Cord
Thymidine
Transforming Growth Factor beta
Animalia
description The Wobbler mouse, a model of amyotrophic lateral sclerosis (ALS), presents motorneuron degeneration and pronounced astrogliosis in the spinal cord. We have studied factors controlling astrocyte proliferation in cultures derived from Wobbler and control mice spinal cord. Basal rate of [3H]thymidine incorporation was 15 times lower in Wobbler astrocytes. While in control cultured cells interleukin-1α (IL-1) and corticosterone (CORT) significantly increased proliferation, both agents were inactive in Wobbler astrocytes. The lack of response to CORT was not due to the absence of glucocorticoid receptors, because similar receptor amounts were found in Wobbler and control astrocytes. In contrast to IL-1 and CORT, transforming growth factor-β1 (TGF-β1) substantially increased proliferation of Wobbler astrocytes but not of control cells. Differences in response to TGF- β1 were also obtained by measuring glial fibrillary acidic protein (GFAP) immunoreaction intensity, which was substantially higher in Wobbler astrocytes. Thus, abnormal responses to different mitogens characterized Wobbler astrocytes in culture. We suggest that TGF-β1 may play a role in the reactive gliosis and GFAP hyperexpression found in the degenerating spinal cord of this model of ALS.
title In vitro differences between astrocytes of control and Wobbler mice spinal cord
title_short In vitro differences between astrocytes of control and Wobbler mice spinal cord
title_full In vitro differences between astrocytes of control and Wobbler mice spinal cord
title_fullStr In vitro differences between astrocytes of control and Wobbler mice spinal cord
title_full_unstemmed In vitro differences between astrocytes of control and Wobbler mice spinal cord
title_sort in vitro differences between astrocytes of control and wobbler mice spinal cord
publishDate 1999
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03643190_v24_n12_p1535_GonzalezDeniselle
http://hdl.handle.net/20.500.12110/paper_03643190_v24_n12_p1535_GonzalezDeniselle
_version_ 1768544914106220544